NP53939.RAQlILes18sxXCMH7bHJminlm83eUGDtjwA6h7le8m9WA
has assertion: NP53939.RAQlILes18sxXCMH7bHJminlm83eUGDtjwA6h7le8m9WA130 assertion
has provenance: NP53939.RAQlILes18sxXCMH7bHJminlm83eUGDtjwA6h7le8m9WA130 provenance
has publication info: NP53939.RAQlILes18sxXCMH7bHJminlm83eUGDtjwA6h7le8m9WA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53939.RAQlILes18sxXCMH7bHJminlm83eUGDtjwA6h7le8m9WA130 assertion
type: Assertion
description: [Our results argue against a major role of NF-M in PD. However, rare variants of the NF-M gene may act as susceptibility factors for PD and functional analyses of the identified variations are warranted to decipher possible mechanisms in NEUROLOGICALeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14583397
was generated by: ECO_0000203

gad-20130706
imported on: 2013-07-06

DisGeNET evidence - LITERATURE
type: ECO_0000212
comment: Gene-disease associations inferred from text-mining the literature.

disgenetrdf
version: v2.1.0

NP53945.RAX6mD0FzHgrTc -h2kF6-zfeHXwopjrCJMOEZh1NTaFQ
has assertion: NP53945.RAX6mD0FzHgrTc -h2kF6-zfeHXwopjrCJMOEZh1NTaFQ130 assertion
has provenance: NP53945.RAX6mD0FzHgrTc -h2kF6-zfeHXwopjrCJMOEZh1NTaFQ130 provenance
has publication info: NP53945.RAX6mD0FzHgrTc -h2kF6-zfeHXwopjrCJMOEZh1NTaFQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53945.RAX6mD0FzHgrTc -h2kF6-zfeHXwopjrCJMOEZh1NTaFQ130 assertion
type: Assertion
description: [Taking into account the above results, as well as those of other studies, it appears that the ND gene mutations can account for 3% of cases of advanced ROP. Although the ND gene is not frequently involved in advanced ROP, the present large-scale study further supports the hypothesis that genetic influences may play an important role in the development of severe ROP in some premature infants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11322656
was generated by: ECO_0000203

NP53949.RASGV0dvTMJFObzesPaELmqn7gsJdZK1GrEcNkB2c1G7s
has assertion: NP53949.RASGV0dvTMJFObzesPaELmqn7gsJdZK1GrEcNkB2c1G7s130 assertion
has provenance: NP53949.RASGV0dvTMJFObzesPaELmqn7gsJdZK1GrEcNkB2c1G7s130 provenance
has publication info: NP53949.RASGV0dvTMJFObzesPaELmqn7gsJdZK1GrEcNkB2c1G7s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53949.RASGV0dvTMJFObzesPaELmqn7gsJdZK1GrEcNkB2c1G7s130 assertion
type: Assertion
description: [ Mutations in the Norrie disease gene can lead to retinal malformations of variable severity both in hemizygous males and manifesting carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/8832723
was generated by: ECO_0000203

NP53960.RAW2lTaUzCUKs0NZAFb-3emzgwfZvOY7DtqijkYZAYahQ
has assertion: NP53960.RAW2lTaUzCUKs0NZAFb-3emzgwfZvOY7DtqijkYZAYahQ130 assertion
has provenance: NP53960.RAW2lTaUzCUKs0NZAFb-3emzgwfZvOY7DtqijkYZAYahQ130 provenance
has publication info: NP53960.RAW2lTaUzCUKs0NZAFb-3emzgwfZvOY7DtqijkYZAYahQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53960.RAW2lTaUzCUKs0NZAFb-3emzgwfZvOY7DtqijkYZAYahQ130 assertion
type: Assertion
description: [ Our results suggest that genetic variations in NCAM1 or nearby genes could confer risks associated with bipolar affective disorder in Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15050861
was generated by: ECO_0000203

NP53966.RAUlNH zCmYHTz9ODMvPB8Q hAb-h02SMtM3KNldz3biI
has assertion: NP53966.RAUlNH zCmYHTz9ODMvPB8Q hAb-h02SMtM3KNldz3biI130 assertion
has provenance: NP53966.RAUlNH zCmYHTz9ODMvPB8Q hAb-h02SMtM3KNldz3biI130 provenance
has publication info: NP53966.RAUlNH zCmYHTz9ODMvPB8Q hAb-h02SMtM3KNldz3biI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53966.RAUlNH zCmYHTz9ODMvPB8Q hAb-h02SMtM3KNldz3biI130 assertion
type: Assertion
description: [Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18676680
was generated by: ECO_0000203

NP53975.RAT30v0JltxwrHLHbwxwqoRyBhNbZ0eeRVGmftjf2nM-U
has assertion: NP53975.RAT30v0JltxwrHLHbwxwqoRyBhNbZ0eeRVGmftjf2nM-U130 assertion
has provenance: NP53975.RAT30v0JltxwrHLHbwxwqoRyBhNbZ0eeRVGmftjf2nM-U130 provenance
has publication info: NP53975.RAT30v0JltxwrHLHbwxwqoRyBhNbZ0eeRVGmftjf2nM-U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53975.RAT30v0JltxwrHLHbwxwqoRyBhNbZ0eeRVGmftjf2nM-U130 assertion
type: Assertion
description: [is that heterozygous germline mutation I171V in NBS1 gene is a significant risk factor for breast cancer development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17899368
was generated by: ECO_0000203

NP53979.RAdMqeRTuCBRuYAxo3L2Fs8mk-4tg9nD3Ygui9cpBWXD4
has assertion: NP53979.RAdMqeRTuCBRuYAxo3L2Fs8mk-4tg9nD3Ygui9cpBWXD4130 assertion
has provenance: NP53979.RAdMqeRTuCBRuYAxo3L2Fs8mk-4tg9nD3Ygui9cpBWXD4130 provenance
has publication info: NP53979.RAdMqeRTuCBRuYAxo3L2Fs8mk-4tg9nD3Ygui9cpBWXD4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53979.RAdMqeRTuCBRuYAxo3L2Fs8mk-4tg9nD3Ygui9cpBWXD4130 assertion
type: Assertion
description: [Analysis of variants in DNA damage signalling genes in bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18638378
was generated by: ECO_0000203

NP53980.RAc4b6hwhyJt6HHARgRz3NF3RROxonUJTVWaIGaiVr8vY
has assertion: NP53980.RAc4b6hwhyJt6HHARgRz3NF3RROxonUJTVWaIGaiVr8vY130 assertion
has provenance: NP53980.RAc4b6hwhyJt6HHARgRz3NF3RROxonUJTVWaIGaiVr8vY130 provenance
has publication info: NP53980.RAc4b6hwhyJt6HHARgRz3NF3RROxonUJTVWaIGaiVr8vY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53980.RAc4b6hwhyJt6HHARgRz3NF3RROxonUJTVWaIGaiVr8vY130 assertion
type: Assertion
description: [our study provides the strongest evidence to date for a role of common variants in DNA repair genes in bladder carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19706757
was generated by: ECO_0000203

NP53981.RAdbZ81kUhSRFBf7okS51zJ9i3xjEAxBewfj4OD q-rNg
has assertion: NP53981.RAdbZ81kUhSRFBf7okS51zJ9i3xjEAxBewfj4OD q-rNg130 assertion
has provenance: NP53981.RAdbZ81kUhSRFBf7okS51zJ9i3xjEAxBewfj4OD q-rNg130 provenance
has publication info: NP53981.RAdbZ81kUhSRFBf7okS51zJ9i3xjEAxBewfj4OD q-rNg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53981.RAdbZ81kUhSRFBf7okS51zJ9i3xjEAxBewfj4OD q-rNg130 assertion
type: Assertion
description: [Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19692168
was generated by: ECO_0000203

NP53986.RAbHguZvMtgeYuBz5IkIv9J7jnpijIQqBly4G-sWNVhBk
has assertion: NP53986.RAbHguZvMtgeYuBz5IkIv9J7jnpijIQqBly4G-sWNVhBk130 assertion
has provenance: NP53986.RAbHguZvMtgeYuBz5IkIv9J7jnpijIQqBly4G-sWNVhBk130 provenance
has publication info: NP53986.RAbHguZvMtgeYuBz5IkIv9J7jnpijIQqBly4G-sWNVhBk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53986.RAbHguZvMtgeYuBz5IkIv9J7jnpijIQqBly4G-sWNVhBk130 assertion
type: Assertion
description: [Haplotypic variation in MRE11, RAD50 and NBS1 and risk of non-Hodgkin's lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17169801
was generated by: ECO_0000203

NP53989.RAb9L3hAt-0XdsFwNjYIBr8YC5Abp8KmE9XP50QNoP4-8
has assertion: NP53989.RAb9L3hAt-0XdsFwNjYIBr8YC5Abp8KmE9XP50QNoP4-8130 assertion
has provenance: NP53989.RAb9L3hAt-0XdsFwNjYIBr8YC5Abp8KmE9XP50QNoP4-8130 provenance
has publication info: NP53989.RAb9L3hAt-0XdsFwNjYIBr8YC5Abp8KmE9XP50QNoP4-8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53989.RAb9L3hAt-0XdsFwNjYIBr8YC5Abp8KmE9XP50QNoP4-8130 assertion
type: Assertion
description: [NAT2 fast acetylator genotype and MGMT promoter methylation may contribute to gender difference in K-RAS mutation occurrence in Taiwanese colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19107910
was generated by: ECO_0000203

NP53995.RAV-XcQbKCOFBBzQpDhKW ymy RcuBJ RFFapR6GQ8FF0
has assertion: NP53995.RAV-XcQbKCOFBBzQpDhKW ymy RcuBJ RFFapR6GQ8FF0130 assertion
has provenance: NP53995.RAV-XcQbKCOFBBzQpDhKW ymy RcuBJ RFFapR6GQ8FF0130 provenance
has publication info: NP53995.RAV-XcQbKCOFBBzQpDhKW ymy RcuBJ RFFapR6GQ8FF0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53995.RAV-XcQbKCOFBBzQpDhKW ymy RcuBJ RFFapR6GQ8FF0130 assertion
type: Assertion
description: [In a multicenter case-control study, 490 colorectal cancer patients and 593 controls (433 matched case-control pairs) were genotyped for common polymorphisms in the cytochrome P450 (CYP1A1, CYP1A2, CYP1B1, CYP2A6, CYP2C9, CYP2C19 and CYP2D6), glutathione S-transferase (GSTM1, GSTP1 and GSTT1), sulfotransferase (SULT1A1 and SULT1A2), N-acetyl transferase 2 (NAT2), NAD(P)H:quinone oxidoreductase (NQO1), methylenetetrahydrofolate reductase (MTHFR), and microsomal epoxide hydrolase (EPHX1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12419832
was generated by: ECO_0000203

NP53999.RAR bZdjiIA8hUilMOSv1azNXiiyUJIvAvb6DU7zGsz5E
has assertion: NP53999.RAR bZdjiIA8hUilMOSv1azNXiiyUJIvAvb6DU7zGsz5E130 assertion
has provenance: NP53999.RAR bZdjiIA8hUilMOSv1azNXiiyUJIvAvb6DU7zGsz5E130 provenance
has publication info: NP53999.RAR bZdjiIA8hUilMOSv1azNXiiyUJIvAvb6DU7zGsz5E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP53999.RAR bZdjiIA8hUilMOSv1azNXiiyUJIvAvb6DU7zGsz5E130 assertion
type: Assertion
description: [Molecular genetic analysis of NBS1 in German melanoma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17496786
was generated by: ECO_0000203

NP54002.RAcS9RcBO0rdQyadHdWtNFalvqnBJQyktQSBxwrkc7Xwk
has assertion: NP54002.RAcS9RcBO0rdQyadHdWtNFalvqnBJQyktQSBxwrkc7Xwk130 assertion
has provenance: NP54002.RAcS9RcBO0rdQyadHdWtNFalvqnBJQyktQSBxwrkc7Xwk130 provenance
has publication info: NP54002.RAcS9RcBO0rdQyadHdWtNFalvqnBJQyktQSBxwrkc7Xwk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54002.RAcS9RcBO0rdQyadHdWtNFalvqnBJQyktQSBxwrkc7Xwk130 assertion
type: Assertion
description: [Even in presence of high alcohol consumption or cigarette smoking, a high intake of fruit and vegetables might prevent the development of around one quarter of SCCHN cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17611777
was generated by: ECO_0000203

NP54003.RAX95PT1sJkjCh8XyHBhOVogH6F2bI-kmRsl50cOm yXo
has assertion: NP54003.RAX95PT1sJkjCh8XyHBhOVogH6F2bI-kmRsl50cOm yXo130 assertion
has provenance: NP54003.RAX95PT1sJkjCh8XyHBhOVogH6F2bI-kmRsl50cOm yXo130 provenance
has publication info: NP54003.RAX95PT1sJkjCh8XyHBhOVogH6F2bI-kmRsl50cOm yXo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54003.RAX95PT1sJkjCh8XyHBhOVogH6F2bI-kmRsl50cOm yXo130 assertion
type: Assertion
description: [In this study the role of genetically determined individual NAT1 and NAT2 genotypes, haplotypes and haplotype combinations in the predisposition to head and neck cancer was investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19898993
was generated by: ECO_0000203

NP54006.RAVKS6SZtH2d27QOPzWRhBS4BMnYZvyfLoHt5XiRt2JnM
has assertion: NP54006.RAVKS6SZtH2d27QOPzWRhBS4BMnYZvyfLoHt5XiRt2JnM130 assertion
has provenance: NP54006.RAVKS6SZtH2d27QOPzWRhBS4BMnYZvyfLoHt5XiRt2JnM130 provenance
has publication info: NP54006.RAVKS6SZtH2d27QOPzWRhBS4BMnYZvyfLoHt5XiRt2JnM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54006.RAVKS6SZtH2d27QOPzWRhBS4BMnYZvyfLoHt5XiRt2JnM130 assertion
type: Assertion
description: [This study integrates epidemiological and clinical data as well as genetic markers along major pathogenic pathways of PTD. The findings from this study should improve our understanding of genetic influences on PTD and gene-environment interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11520401
was generated by: ECO_0000203

NP54007.RAYLQ41ATV306HVfBlxlXPXP4M9uDPp42m9-EeTDTjHFc
has assertion: NP54007.RAYLQ41ATV306HVfBlxlXPXP4M9uDPp42m9-EeTDTjHFc130 assertion
has provenance: NP54007.RAYLQ41ATV306HVfBlxlXPXP4M9uDPp42m9-EeTDTjHFc130 provenance
has publication info: NP54007.RAYLQ41ATV306HVfBlxlXPXP4M9uDPp42m9-EeTDTjHFc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54007.RAYLQ41ATV306HVfBlxlXPXP4M9uDPp42m9-EeTDTjHFc130 assertion
type: Assertion
description: [No differences in allele frequencies were seen by age, sex, or type of controls (hospital patients versus population controls). No examples of linkage disequilibrium between the different loci were detected based on comparison of observed and expected frequencies for combinations of specific alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11751440
was generated by: ECO_0000203

NP54014.RAbpaaDWu0 WzUIRi 1HxrDghSt-tNrWGV2KlYwnhQJcg
has assertion: NP54014.RAbpaaDWu0 WzUIRi 1HxrDghSt-tNrWGV2KlYwnhQJcg130 assertion
has provenance: NP54014.RAbpaaDWu0 WzUIRi 1HxrDghSt-tNrWGV2KlYwnhQJcg130 provenance
has publication info: NP54014.RAbpaaDWu0 WzUIRi 1HxrDghSt-tNrWGV2KlYwnhQJcg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54014.RAbpaaDWu0 WzUIRi 1HxrDghSt-tNrWGV2KlYwnhQJcg130 assertion
type: Assertion
description: [The NAT2 slow acetylator phenotype/genotype has been inconsistently associated with lung cancer and, to date, the role of NAT1 polymorphism in lung cancer has not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9731715
was generated by: ECO_0000203

NP54016.RAUXc9ucd6Jj wyPIDdlJKWSP86vVDtwPKpQK LCgLMg8
has assertion: NP54016.RAUXc9ucd6Jj wyPIDdlJKWSP86vVDtwPKpQK LCgLMg8130 assertion
has provenance: NP54016.RAUXc9ucd6Jj wyPIDdlJKWSP86vVDtwPKpQK LCgLMg8130 provenance
has publication info: NP54016.RAUXc9ucd6Jj wyPIDdlJKWSP86vVDtwPKpQK LCgLMg8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54016.RAUXc9ucd6Jj wyPIDdlJKWSP86vVDtwPKpQK LCgLMg8130 assertion
type: Assertion
description: [Lung cancer susceptibility model based on age, family history and genetic variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19390575
was generated by: ECO_0000203

NP54018.RAXeTeaB1qj0jEjSKHWBd0ulvv7H3rnJGFSJxBx5cf57I
has assertion: NP54018.RAXeTeaB1qj0jEjSKHWBd0ulvv7H3rnJGFSJxBx5cf57I130 assertion
has provenance: NP54018.RAXeTeaB1qj0jEjSKHWBd0ulvv7H3rnJGFSJxBx5cf57I130 provenance
has publication info: NP54018.RAXeTeaB1qj0jEjSKHWBd0ulvv7H3rnJGFSJxBx5cf57I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54018.RAXeTeaB1qj0jEjSKHWBd0ulvv7H3rnJGFSJxBx5cf57I130 assertion
type: Assertion
description: [The aim of this study was to determine the existence of association between the genetic polymorphisms of metabolizing genes GSTM-1, GSTT-1, and NAT-2, and the presence of mitochondrial genome instability (mtGI) in breast cancer cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19287511
was generated by: ECO_0000203

NP54019.RASQfH7HTm1oaMIp9Ehi-3wly8da0OezF8KR43ifGxx64
has assertion: NP54019.RASQfH7HTm1oaMIp9Ehi-3wly8da0OezF8KR43ifGxx64130 assertion
has provenance: NP54019.RASQfH7HTm1oaMIp9Ehi-3wly8da0OezF8KR43ifGxx64130 provenance
has publication info: NP54019.RASQfH7HTm1oaMIp9Ehi-3wly8da0OezF8KR43ifGxx64130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54019.RASQfH7HTm1oaMIp9Ehi-3wly8da0OezF8KR43ifGxx64130 assertion
type: Assertion
description: [Meat consumption, heterocyclic amines, NAT2, and the risk of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19116874
was generated by: ECO_0000203

NP54023.RAQ9iZKMTNiIktLfnlktkE9ZkbFW5jSEfqa2mKweGyGeM
has assertion: NP54023.RAQ9iZKMTNiIktLfnlktkE9ZkbFW5jSEfqa2mKweGyGeM130 assertion
has provenance: NP54023.RAQ9iZKMTNiIktLfnlktkE9ZkbFW5jSEfqa2mKweGyGeM130 provenance
has publication info: NP54023.RAQ9iZKMTNiIktLfnlktkE9ZkbFW5jSEfqa2mKweGyGeM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54023.RAQ9iZKMTNiIktLfnlktkE9ZkbFW5jSEfqa2mKweGyGeM130 assertion
type: Assertion
description: [NAT2 polymorphisms combining with smoking associated with breast cancer susceptibility: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20180012
was generated by: ECO_0000203

NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV NIyndo
has assertion: NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV NIyndo130 assertion
has provenance: NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV NIyndo130 provenance
has publication info: NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV NIyndo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV NIyndo130 assertion
type: Assertion
description: [The distribution of NAT2 activity in the healthy control group was found to be correlated with that of healthy caucasians. Patients had slow acetylator phenotypes of NAT2, 1.8 times higher than controls but no statistical differences were found (p=0.07). In addition, the NAT2*5 alelle was more statistically correlated with breast cancer patients rather than the controls (p=0.02). Moreover, NAT2*5B was the most frequent haplotype of the NAT2*5 family (p=0.000). Breast cancer patients were detected to posses more CYP1B1*3 mutant alleles than the controls (p=0.043). The combined effect of CYP1B1*3 polymorphism and NAT2 slow acetylator genotype contributed to an increased risk for breast cancer in patients in this study (p=0.004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20683028
was generated by: ECO_0000203

NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI
has assertion: NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130 assertion
has provenance: NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130 provenance
has publication info: NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130 assertion
type: Assertion
description: [Statistically significant increases in asthma risk were also observed among the whole study population for the concurrent presence of the GSTM1 null genotype and either NAT1 (odds ratio OR 4.53, 95% CI 1.76 to 11.6) or NAT2 (OR 3.12, 95% CI 1.11 to 8.78) slow acetylator genotypes, and of NAT1 and NAT2 slow acetylator genotypes (OR 4.20, 95% CI 1.51 to 11.6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11927838
was generated by: ECO_0000203

NP54031.RAZWqqm48jF-vyQ6efJOttIlrUqdYx1OiOMixDiuOIqtk
has assertion: NP54031.RAZWqqm48jF-vyQ6efJOttIlrUqdYx1OiOMixDiuOIqtk130 assertion
has provenance: NP54031.RAZWqqm48jF-vyQ6efJOttIlrUqdYx1OiOMixDiuOIqtk130 provenance
has publication info: NP54031.RAZWqqm48jF-vyQ6efJOttIlrUqdYx1OiOMixDiuOIqtk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54031.RAZWqqm48jF-vyQ6efJOttIlrUqdYx1OiOMixDiuOIqtk130 assertion
type: Assertion
description: [This study shows an association between acetylation polymorphism and susceptibility to extrinsic asthma, but not to intrinsic asthma, suggesting a minor role of the NAT2 polymorphism in the development of atopic asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12492617
was generated by: ECO_0000203

NP54035.RAZdzAmNg0aK6H1N-6hd4aWAj0dYwg-td4xKl8cifImlw
has assertion: NP54035.RAZdzAmNg0aK6H1N-6hd4aWAj0dYwg-td4xKl8cifImlw130 assertion
has provenance: NP54035.RAZdzAmNg0aK6H1N-6hd4aWAj0dYwg-td4xKl8cifImlw130 provenance
has publication info: NP54035.RAZdzAmNg0aK6H1N-6hd4aWAj0dYwg-td4xKl8cifImlw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54035.RAZdzAmNg0aK6H1N-6hd4aWAj0dYwg-td4xKl8cifImlw130 assertion
type: Assertion
description: [Individuals with NAT2 slow acetylator genotypes had a significant increase in risk of BC compared to individuals with NAT2 rapid acetylators (OR adjusted for smoking status=2.70; 95% CI, 1.10-6.61).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19443378
was generated by: ECO_0000203

NP54037.RAcUoCQbOBlpKEByqod6ke arnm7V0T3g75DV8tDflthE
has assertion: NP54037.RAcUoCQbOBlpKEByqod6ke arnm7V0T3g75DV8tDflthE130 assertion
has provenance: NP54037.RAcUoCQbOBlpKEByqod6ke arnm7V0T3g75DV8tDflthE130 provenance
has publication info: NP54037.RAcUoCQbOBlpKEByqod6ke arnm7V0T3g75DV8tDflthE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54037.RAcUoCQbOBlpKEByqod6ke arnm7V0T3g75DV8tDflthE130 assertion
type: Assertion
description: [Bladder cancer, GSTs, NAT1, NAT2, SULT1A1, XRCC1, XRCC3, XPD genetic polymorphisms and coffee consumption: a case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18365755
was generated by: ECO_0000203

NP54044.RAY76q9CUIU4v9PHlfRQ7mwV1hYw05BZoSTsbDv3yAs8E
has assertion: NP54044.RAY76q9CUIU4v9PHlfRQ7mwV1hYw05BZoSTsbDv3yAs8E130 assertion
has provenance: NP54044.RAY76q9CUIU4v9PHlfRQ7mwV1hYw05BZoSTsbDv3yAs8E130 provenance
has publication info: NP54044.RAY76q9CUIU4v9PHlfRQ7mwV1hYw05BZoSTsbDv3yAs8E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54044.RAY76q9CUIU4v9PHlfRQ7mwV1hYw05BZoSTsbDv3yAs8E130 assertion
type: Assertion
description: [Polymorphysms of the three genes encoding phase 1 (CYP1A1, mEPH1, and CYP2E2) and the three genes encoding phase 2 (NAT2, GSTM1, and GSTT1) xenobiotic detoxication enzymes were typed by use of PCR in 74 patients with extragenital endometriosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12760253
was generated by: ECO_0000203

NP54047.RAQrVoXLAD-rr0NUFlexcRg5iY0Yh7LLJVaM98WW7az3k
has assertion: NP54047.RAQrVoXLAD-rr0NUFlexcRg5iY0Yh7LLJVaM98WW7az3k130 assertion
has provenance: NP54047.RAQrVoXLAD-rr0NUFlexcRg5iY0Yh7LLJVaM98WW7az3k130 provenance
has publication info: NP54047.RAQrVoXLAD-rr0NUFlexcRg5iY0Yh7LLJVaM98WW7az3k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54047.RAQrVoXLAD-rr0NUFlexcRg5iY0Yh7LLJVaM98WW7az3k130 assertion
type: Assertion
description: [We conclude that the two polymorphisms, GSTT1 null and PON1 BB, are common genetic traits that pose low individual risk but may be important determinants of overall population NHL risk, particularly among groups exposed to NHL-related carcinogens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12139735
was generated by: ECO_0000203

NP54052.RAZY3aBcViMzrP3UGiwUg-AUdcs3YknI8oZr25E3UNFpM
has assertion: NP54052.RAZY3aBcViMzrP3UGiwUg-AUdcs3YknI8oZr25E3UNFpM130 assertion
has provenance: NP54052.RAZY3aBcViMzrP3UGiwUg-AUdcs3YknI8oZr25E3UNFpM130 provenance
has publication info: NP54052.RAZY3aBcViMzrP3UGiwUg-AUdcs3YknI8oZr25E3UNFpM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54052.RAZY3aBcViMzrP3UGiwUg-AUdcs3YknI8oZr25E3UNFpM130 assertion
type: Assertion
description: [Polymorphisms of cytochrome P4501A2 and N-acetyltransferase genes, smoking, and risk of pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15987714
was generated by: ECO_0000203

NP54074.RAfZ4BcKrsNaXM10cFJ4eq7krWULsc7oWXmQfgjBw3E1g
has assertion: NP54074.RAfZ4BcKrsNaXM10cFJ4eq7krWULsc7oWXmQfgjBw3E1g130 assertion
has provenance: NP54074.RAfZ4BcKrsNaXM10cFJ4eq7krWULsc7oWXmQfgjBw3E1g130 provenance
has publication info: NP54074.RAfZ4BcKrsNaXM10cFJ4eq7krWULsc7oWXmQfgjBw3E1g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54074.RAfZ4BcKrsNaXM10cFJ4eq7krWULsc7oWXmQfgjBw3E1g130 assertion
type: Assertion
description: [We examine whether there was a correlation between diplotype configurations (combinations of 2 haplotypes for a subject) at the NAT2 gene and the adverse effects of SSZ used for the treatment of rheumatoid arthritis (RA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12465141
was generated by: ECO_0000203

NP54075.RAV2bHA3R5ppd6Mldd3q6O-Xw0bTId3RRnPGTawoSPx5Y
has assertion: NP54075.RAV2bHA3R5ppd6Mldd3q6O-Xw0bTId3RRnPGTawoSPx5Y130 assertion
has provenance: NP54075.RAV2bHA3R5ppd6Mldd3q6O-Xw0bTId3RRnPGTawoSPx5Y130 provenance
has publication info: NP54075.RAV2bHA3R5ppd6Mldd3q6O-Xw0bTId3RRnPGTawoSPx5Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54075.RAV2bHA3R5ppd6Mldd3q6O-Xw0bTId3RRnPGTawoSPx5Y130 assertion
type: Assertion
description: [In a preliminary report we demonstrated an association between the slow acetylator genotype of N-acetyltransferase 2 (NAT2) and familial cases of Parkinson's disease (FPD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10634239
was generated by: ECO_0000203

NP54087.RAYRFzqy3kkyL7jTeSjK 3i9u9GK6Sr4HTOpHf61u1Sh8
has assertion: NP54087.RAYRFzqy3kkyL7jTeSjK 3i9u9GK6Sr4HTOpHf61u1Sh8130 assertion
has provenance: NP54087.RAYRFzqy3kkyL7jTeSjK 3i9u9GK6Sr4HTOpHf61u1Sh8130 provenance
has publication info: NP54087.RAYRFzqy3kkyL7jTeSjK 3i9u9GK6Sr4HTOpHf61u1Sh8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54087.RAYRFzqy3kkyL7jTeSjK 3i9u9GK6Sr4HTOpHf61u1Sh8130 assertion
type: Assertion
description: [For tumor protein 53 (TP53), N-acetyl transferase 1 (NAT1), NAT2, glutathione-S transferase Mu (GSTM1), glutathione-S transferase Theta (GSTT1), and glutathione-S transferase Pi (GSTP1) polymorphisms, the best estimates are sufficient to exclude a 1.7-fold increase in risk of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11487538
was generated by: ECO_0000203

NP54088.RAU9bTMr0BtthfHCko4DegagXIYt8e2f-O-BMS35mfrlU
has assertion: NP54088.RAU9bTMr0BtthfHCko4DegagXIYt8e2f-O-BMS35mfrlU130 assertion
has provenance: NP54088.RAU9bTMr0BtthfHCko4DegagXIYt8e2f-O-BMS35mfrlU130 provenance
has publication info: NP54088.RAU9bTMr0BtthfHCko4DegagXIYt8e2f-O-BMS35mfrlU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54088.RAU9bTMr0BtthfHCko4DegagXIYt8e2f-O-BMS35mfrlU130 assertion
type: Assertion
description: [The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20437058
was generated by: ECO_0000203

NP54094.RAZfStK KvpU9zTihspCIhZJsFQcB3zfX6pttG1QWTFxs
has assertion: NP54094.RAZfStK KvpU9zTihspCIhZJsFQcB3zfX6pttG1QWTFxs130 assertion
has provenance: NP54094.RAZfStK KvpU9zTihspCIhZJsFQcB3zfX6pttG1QWTFxs130 provenance
has publication info: NP54094.RAZfStK KvpU9zTihspCIhZJsFQcB3zfX6pttG1QWTFxs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54094.RAZfStK KvpU9zTihspCIhZJsFQcB3zfX6pttG1QWTFxs130 assertion
type: Assertion
description: [Gene-environment interactions in pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12120227
was generated by: ECO_0000203

NP54095.RATC9ZMzH4PLZYGgtz1unLkKitu0wnt50boYSeZfeW3uo
has assertion: NP54095.RATC9ZMzH4PLZYGgtz1unLkKitu0wnt50boYSeZfeW3uo130 assertion
has provenance: NP54095.RATC9ZMzH4PLZYGgtz1unLkKitu0wnt50boYSeZfeW3uo130 provenance
has publication info: NP54095.RATC9ZMzH4PLZYGgtz1unLkKitu0wnt50boYSeZfeW3uo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54095.RATC9ZMzH4PLZYGgtz1unLkKitu0wnt50boYSeZfeW3uo130 assertion
type: Assertion
description: [No significant correlation was found between the level of 8-OH-dG and the MnSOD, GSTM1, and hOGG1 polymorphisms. However, one novel polymorphism/mutation of the hOGG1 gene was found in a pancreatic tumor. Mutation at codon 12 of the K-ras gene was found in 25 (81%) of 31 pancreatic tumors, including three G-to-A transitions and 22 G-to-T transversions. Patients with the G-to-T mutation had a significantly higher level of aromatic DNA adducts than those with G-to-A or wild-type codon (P=0.02). On the other hand, the K-ras mutation profile was not related to the level of 8-OH-dG. Given the limitation of sample size, these preliminary data lend further support the hypothesis that carcinogen exposure and oxidative stress are involved in pancreatic carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11719088
was generated by: ECO_0000203

NP54099.RAZk3mDwR5Kie3aYaFkqDjwN6 sAb rfiE5tLO Wpkb1s
has assertion: NP54099.RAZk3mDwR5Kie3aYaFkqDjwN6 sAb rfiE5tLO Wpkb1s130 assertion
has provenance: NP54099.RAZk3mDwR5Kie3aYaFkqDjwN6 sAb rfiE5tLO Wpkb1s130 provenance
has publication info: NP54099.RAZk3mDwR5Kie3aYaFkqDjwN6 sAb rfiE5tLO Wpkb1s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54099.RAZk3mDwR5Kie3aYaFkqDjwN6 sAb rfiE5tLO Wpkb1s130 assertion
type: Assertion
description: [The associations between the genotypes of glutathione S-transferase (GST) M1, GSTP1, GSTT1 and N-acetyltransferase (NAT) 1 and the phenotypes of NAT2 and cytochrome P450 (CYP) 1A2 and bladder cancer risk were examined in a case-control study involving 731 bladder cancer patients and 740 control subjects in Los Angeles County, California.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18544563
was generated by: ECO_0000203

NP54105.RAbWsJYtHhcXjn4FdsTo3STSa Vntuf3u17RtHL-kSH64
has assertion: NP54105.RAbWsJYtHhcXjn4FdsTo3STSa Vntuf3u17RtHL-kSH64130 assertion
has provenance: NP54105.RAbWsJYtHhcXjn4FdsTo3STSa Vntuf3u17RtHL-kSH64130 provenance
has publication info: NP54105.RAbWsJYtHhcXjn4FdsTo3STSa Vntuf3u17RtHL-kSH64130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54105.RAbWsJYtHhcXjn4FdsTo3STSa Vntuf3u17RtHL-kSH64130 assertion
type: Assertion
description: [our findings suggest a very limited role, if any, of genetic polymorphisms investigated in modulating the BC risk in coffee drinkers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18365755
was generated by: ECO_0000203

NP54106.RAdrcWsK509YILHdqZwgh-58X Vu8RK4AJQt YivDGIx8
has assertion: NP54106.RAdrcWsK509YILHdqZwgh-58X Vu8RK4AJQt YivDGIx8130 assertion
has provenance: NP54106.RAdrcWsK509YILHdqZwgh-58X Vu8RK4AJQt YivDGIx8130 provenance
has publication info: NP54106.RAdrcWsK509YILHdqZwgh-58X Vu8RK4AJQt YivDGIx8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54106.RAdrcWsK509YILHdqZwgh-58X Vu8RK4AJQt YivDGIx8130 assertion
type: Assertion
description: [NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16112301
was generated by: ECO_0000203

NP54107.RAdqNn-2F8iggvFURR FphS5Z3Pkktl4-kPRGFeFOqc A
has assertion: NP54107.RAdqNn-2F8iggvFURR FphS5Z3Pkktl4-kPRGFeFOqc A130 assertion
has provenance: NP54107.RAdqNn-2F8iggvFURR FphS5Z3Pkktl4-kPRGFeFOqc A130 provenance
has publication info: NP54107.RAdqNn-2F8iggvFURR FphS5Z3Pkktl4-kPRGFeFOqc A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54107.RAdqNn-2F8iggvFURR FphS5Z3Pkktl4-kPRGFeFOqc A130 assertion
type: Assertion
description: [These data suggest that CYP1A1*4, NAT1 and NAT2 variants are involved in the susceptibility to breast carcinoma by modifying the impact of exogenous and/or endogenous exposures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11291049
was generated by: ECO_0000203

NP54112.RAb6dF4mVRCGI2OGX8tvISEZ1cDAV3x1RIcmmOngtGqTA
has assertion: NP54112.RAb6dF4mVRCGI2OGX8tvISEZ1cDAV3x1RIcmmOngtGqTA130 assertion
has provenance: NP54112.RAb6dF4mVRCGI2OGX8tvISEZ1cDAV3x1RIcmmOngtGqTA130 provenance
has publication info: NP54112.RAb6dF4mVRCGI2OGX8tvISEZ1cDAV3x1RIcmmOngtGqTA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54112.RAb6dF4mVRCGI2OGX8tvISEZ1cDAV3x1RIcmmOngtGqTA130 assertion
type: Assertion
description: [Overall, there is no conclusive evidence that genetic variants in genes involved in the estrogen metabolic pathway are associated with mammographic density in postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20214802
was generated by: ECO_0000203

NP54123.RAapXg46gOMX44MN-0wNtOl1z2kuioskeskOl6jjTPYik
has assertion: NP54123.RAapXg46gOMX44MN-0wNtOl1z2kuioskeskOl6jjTPYik130 assertion
has provenance: NP54123.RAapXg46gOMX44MN-0wNtOl1z2kuioskeskOl6jjTPYik130 provenance
has publication info: NP54123.RAapXg46gOMX44MN-0wNtOl1z2kuioskeskOl6jjTPYik130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54123.RAapXg46gOMX44MN-0wNtOl1z2kuioskeskOl6jjTPYik130 assertion
type: Assertion
description: [Case-control study of genotypes in multiple chemical sensitivity: CYP2D6, NAT1, NAT2, PON1, PON2 and MTHFR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15256524
was generated by: ECO_0000203

NP54128.RAa1NG94xxhb1IFtk7JZWlRrjpHbHCIw4MEYbIHEReOus
has assertion: NP54128.RAa1NG94xxhb1IFtk7JZWlRrjpHbHCIw4MEYbIHEReOus130 assertion
has provenance: NP54128.RAa1NG94xxhb1IFtk7JZWlRrjpHbHCIw4MEYbIHEReOus130 provenance
has publication info: NP54128.RAa1NG94xxhb1IFtk7JZWlRrjpHbHCIw4MEYbIHEReOus130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54128.RAa1NG94xxhb1IFtk7JZWlRrjpHbHCIw4MEYbIHEReOus130 assertion
type: Assertion
description: [Results of exploratory analyses of the data suggest that the association of PCA and MnSOD exists only in the subpopulation of rapid NAT1 genotypes and smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19368118
was generated by: ECO_0000203

NP54134.RAc5RKoLUWwv1wogpv5t6QI7pPhAhQVYZ5AXJjXJdUjac
has assertion: NP54134.RAc5RKoLUWwv1wogpv5t6QI7pPhAhQVYZ5AXJjXJdUjac130 assertion
has provenance: NP54134.RAc5RKoLUWwv1wogpv5t6QI7pPhAhQVYZ5AXJjXJdUjac130 provenance
has publication info: NP54134.RAc5RKoLUWwv1wogpv5t6QI7pPhAhQVYZ5AXJjXJdUjac130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54134.RAc5RKoLUWwv1wogpv5t6QI7pPhAhQVYZ5AXJjXJdUjac130 assertion
type: Assertion
description: [Based on these observations, a screening strategy of MYOC mutations in French POAG patients is briefly outlined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12872267
was generated by: ECO_0000203

NP54135.RASTerb5wd3c PTFCFkYQzCm9ADexxX9dPTCCstPlofJU
has assertion: NP54135.RASTerb5wd3c PTFCFkYQzCm9ADexxX9dPTCCstPlofJU130 assertion
has provenance: NP54135.RASTerb5wd3c PTFCFkYQzCm9ADexxX9dPTCCstPlofJU130 provenance
has publication info: NP54135.RASTerb5wd3c PTFCFkYQzCm9ADexxX9dPTCCstPlofJU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54135.RASTerb5wd3c PTFCFkYQzCm9ADexxX9dPTCCstPlofJU130 assertion
type: Assertion
description: [The absence of the POAG-associated Q368X mutation and the presence of particular polymorphisms, including P13P + L159L and T325T, could be specific features of the MYOC sequence in African populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12868033
was generated by: ECO_0000203

NP54137.RAUKniJneLRm t9SVhMrQ A4 DWuUMvqfORZnqEtN5s7E
has assertion: NP54137.RAUKniJneLRm t9SVhMrQ A4 DWuUMvqfORZnqEtN5s7E130 assertion
has provenance: NP54137.RAUKniJneLRm t9SVhMrQ A4 DWuUMvqfORZnqEtN5s7E130 provenance
has publication info: NP54137.RAUKniJneLRm t9SVhMrQ A4 DWuUMvqfORZnqEtN5s7E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54137.RAUKniJneLRm t9SVhMrQ A4 DWuUMvqfORZnqEtN5s7E130 assertion
type: Assertion
description: [The GLC1A Thr377Met mutation is associated with POAG that, in the pedigrees studied, had a younger age at onset and higher peak intraocular pressure than in pedigrees with the more common Gln368STOP mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12912696
was generated by: ECO_0000203

NP54143.RAeNXQYHZWJXMvHws0aeSOq1jfwWbAPYoArCuyLrmn7cc
has assertion: NP54143.RAeNXQYHZWJXMvHws0aeSOq1jfwWbAPYoArCuyLrmn7cc130 assertion
has provenance: NP54143.RAeNXQYHZWJXMvHws0aeSOq1jfwWbAPYoArCuyLrmn7cc130 provenance
has publication info: NP54143.RAeNXQYHZWJXMvHws0aeSOq1jfwWbAPYoArCuyLrmn7cc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54143.RAeNXQYHZWJXMvHws0aeSOq1jfwWbAPYoArCuyLrmn7cc130 assertion
type: Assertion
description: [Our findings indicate that the mutation frequency of the MYOC gene is 2% in the Indian population affected with POAG, which is not a well-studied ethnic group of the Asian continent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14627955
was generated by: ECO_0000203

NP54149.RASWsXYAqi-UuzIN0PvPoY32hrLn692TVQjaXWT9V2U3g
has assertion: NP54149.RASWsXYAqi-UuzIN0PvPoY32hrLn692TVQjaXWT9V2U3g130 assertion
has provenance: NP54149.RASWsXYAqi-UuzIN0PvPoY32hrLn692TVQjaXWT9V2U3g130 provenance
has publication info: NP54149.RASWsXYAqi-UuzIN0PvPoY32hrLn692TVQjaXWT9V2U3g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54149.RASWsXYAqi-UuzIN0PvPoY32hrLn692TVQjaXWT9V2U3g130 assertion
type: Assertion
description: [Mutations in MYL2 could be associated with both benign and malignant HCM phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12404107
was generated by: ECO_0000203

NP54154.RAfv9eu-bYhrTIG2y8nw-SAXY57MMuOPNVzk4bIKpn5EY
has assertion: NP54154.RAfv9eu-bYhrTIG2y8nw-SAXY57MMuOPNVzk4bIKpn5EY130 assertion
has provenance: NP54154.RAfv9eu-bYhrTIG2y8nw-SAXY57MMuOPNVzk4bIKpn5EY130 provenance
has publication info: NP54154.RAfv9eu-bYhrTIG2y8nw-SAXY57MMuOPNVzk4bIKpn5EY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54154.RAfv9eu-bYhrTIG2y8nw-SAXY57MMuOPNVzk4bIKpn5EY130 assertion
type: Assertion
description: [We investigated 100 independent patients with HCM (proband 51, sporadic 49) by sequencing the three most frequent HCM-causing genes (MYH7, MYBPC3, TNNT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15563892
was generated by: ECO_0000203

NP54156.RAbZm0LDzp D61oTF sIvZJeQfbRdk 2oJOKCb-GFh1II
has assertion: NP54156.RAbZm0LDzp D61oTF sIvZJeQfbRdk 2oJOKCb-GFh1II130 assertion
has provenance: NP54156.RAbZm0LDzp D61oTF sIvZJeQfbRdk 2oJOKCb-GFh1II130 provenance
has publication info: NP54156.RAbZm0LDzp D61oTF sIvZJeQfbRdk 2oJOKCb-GFh1II130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54156.RAbZm0LDzp D61oTF sIvZJeQfbRdk 2oJOKCb-GFh1II130 assertion
type: Assertion
description: [Genetic screening of the beta-myosin heavy chain gene (MYH7) was evaluated in 100 consecutive unrelated patients with hypertrophic cardiomyopathy (HCM) and 200 normal unrelated subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12820698
was generated by: ECO_0000203

NP54158.RATRivlNUZ8t4pnn295mzfUEQWKrPlOc JIee24ko-erk
has assertion: NP54158.RATRivlNUZ8t4pnn295mzfUEQWKrPlOc JIee24ko-erk130 assertion
has provenance: NP54158.RATRivlNUZ8t4pnn295mzfUEQWKrPlOc JIee24ko-erk130 provenance
has publication info: NP54158.RATRivlNUZ8t4pnn295mzfUEQWKrPlOc JIee24ko-erk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54158.RATRivlNUZ8t4pnn295mzfUEQWKrPlOc JIee24ko-erk130 assertion
type: Assertion
description: [left ventricular noncompaction is within the diverse spectrum of cardiac morphologies triggered by sarcomere protein gene defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18506004
was generated by: ECO_0000203

NP54176.RAU1ou fOwJTEzN87dq-PEzAFH42ZF fYTnfm2vnYNoME
has assertion: NP54176.RAU1ou fOwJTEzN87dq-PEzAFH42ZF fYTnfm2vnYNoME130 assertion
has provenance: NP54176.RAU1ou fOwJTEzN87dq-PEzAFH42ZF fYTnfm2vnYNoME130 provenance
has publication info: NP54176.RAU1ou fOwJTEzN87dq-PEzAFH42ZF fYTnfm2vnYNoME130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54176.RAU1ou fOwJTEzN87dq-PEzAFH42ZF fYTnfm2vnYNoME130 assertion
type: Assertion
description: [The breast cancer risk associated with this genotype increases above the age of 50 years (OR = 2.24, 95% CI 1.20-4.21, p = 0.012). The wild-type amino acid Asn of this polymorphism is located in the N-terminal MYC transactivation domain and is highly conserved not only among most diverse species but also in the N-MYC homologue. Due to the pivotal role of c-MYC in diverse tumours, this variant might affect the genetic susceptibility of other cancers as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15929079
was generated by: ECO_0000203

NP54177.RAejqF-uIRL42PgYjdO7ZrAh0JtrDNCQ4yuEw8av3hgvg
has assertion: NP54177.RAejqF-uIRL42PgYjdO7ZrAh0JtrDNCQ4yuEw8av3hgvg130 assertion
has provenance: NP54177.RAejqF-uIRL42PgYjdO7ZrAh0JtrDNCQ4yuEw8av3hgvg130 provenance
has publication info: NP54177.RAejqF-uIRL42PgYjdO7ZrAh0JtrDNCQ4yuEw8av3hgvg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54177.RAejqF-uIRL42PgYjdO7ZrAh0JtrDNCQ4yuEw8av3hgvg130 assertion
type: Assertion
description: [Further work is recommended to understand the potential functional role of these specific non-synonymous amino acid changes and a larger, more comprehensive investigation of genetic variation in these genes (e.g., using a tagSNP approach) in combination with other relevant genes is needed as well as consideration for treatment effects when assessing their po]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17567920
was generated by: ECO_0000203

NP54186.RAerFfKMW3Km87DQ4VN2la9UX2PubPGelUat82iMV3UL0
has assertion: NP54186.RAerFfKMW3Km87DQ4VN2la9UX2PubPGelUat82iMV3UL0130 assertion
has provenance: NP54186.RAerFfKMW3Km87DQ4VN2la9UX2PubPGelUat82iMV3UL0130 provenance
has publication info: NP54186.RAerFfKMW3Km87DQ4VN2la9UX2PubPGelUat82iMV3UL0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54186.RAerFfKMW3Km87DQ4VN2la9UX2PubPGelUat82iMV3UL0130 assertion
type: Assertion
description: [ This study defines the frequency and associated phenotype for MYBPC3 and/or multiple mutations in HCM in the largest cohort to date. In this cohort, unrelated patients with MYBPC3-HCM virtually mimicked the phenotype of those with mutations in the beta-myosin heavy chain. Patients with multiple mutations had the most severe phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15519027
was generated by: ECO_0000203

NP54199.RAbf7zssvi50ZeWEInv05nj akWcBEDiAEhiZ3uWglygE
has assertion: NP54199.RAbf7zssvi50ZeWEInv05nj akWcBEDiAEhiZ3uWglygE130 assertion
has provenance: NP54199.RAbf7zssvi50ZeWEInv05nj akWcBEDiAEhiZ3uWglygE130 provenance
has publication info: NP54199.RAbf7zssvi50ZeWEInv05nj akWcBEDiAEhiZ3uWglygE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54199.RAbf7zssvi50ZeWEInv05nj akWcBEDiAEhiZ3uWglygE130 assertion
type: Assertion
description: [Our findings suggest that polymorphisms of two IFN-inducible genes OAS-1 and MxA might affect susceptibility to the disease and progression of SARS at each level.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15766558
was generated by: ECO_0000203

NP54201.RAXJqXwvAahVow43yUcjoRcmr3B-jITBcaQT-Fr-UlzvQ
has assertion: NP54201.RAXJqXwvAahVow43yUcjoRcmr3B-jITBcaQT-Fr-UlzvQ130 assertion
has provenance: NP54201.RAXJqXwvAahVow43yUcjoRcmr3B-jITBcaQT-Fr-UlzvQ130 provenance
has publication info: NP54201.RAXJqXwvAahVow43yUcjoRcmr3B-jITBcaQT-Fr-UlzvQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54201.RAXJqXwvAahVow43yUcjoRcmr3B-jITBcaQT-Fr-UlzvQ130 assertion
type: Assertion
description: [ MxA promoter -88 G/T SNP may confer host genetic susceptibility to SSPE in Japanese individuals. The finding that homozygotes of the MxA -88T allele with a high MxA-producing capability were more frequently seen in SSPE patients suggests that the MxA protein promotes the establishment of persistent MV infection of neural cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14872030
was generated by: ECO_0000203

NP54206.RAcDuG7bNUoa-W9qubRZINX5besqHY AiZpvGvr6BstHk
has assertion: NP54206.RAcDuG7bNUoa-W9qubRZINX5besqHY AiZpvGvr6BstHk130 assertion
has provenance: NP54206.RAcDuG7bNUoa-W9qubRZINX5besqHY AiZpvGvr6BstHk130 provenance
has publication info: NP54206.RAcDuG7bNUoa-W9qubRZINX5besqHY AiZpvGvr6BstHk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54206.RAcDuG7bNUoa-W9qubRZINX5besqHY AiZpvGvr6BstHk130 assertion
type: Assertion
description: [Approximately 69% of the excess familial risk in FDRs can be ascribed to MSS CRC, and although the pattern of familial risk supports recessive susceptibility in addition to MUTYH, the absolute risk of CRC is at best modest.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19307499
was generated by: ECO_0000203

NP54213.RAbYTcQ sZuhBcBc8 lFFpb5ELqNImvBQvtQ5uPaa9xaQ
has assertion: NP54213.RAbYTcQ sZuhBcBc8 lFFpb5ELqNImvBQvtQ5uPaa9xaQ130 assertion
has provenance: NP54213.RAbYTcQ sZuhBcBc8 lFFpb5ELqNImvBQvtQ5uPaa9xaQ130 provenance
has publication info: NP54213.RAbYTcQ sZuhBcBc8 lFFpb5ELqNImvBQvtQ5uPaa9xaQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54213.RAbYTcQ sZuhBcBc8 lFFpb5ELqNImvBQvtQ5uPaa9xaQ130 assertion
type: Assertion
description: [The results reveal that MYH accounts for 16 percent of polyposis patients without germline mutations in the APC gene and that it does not appear to be a modifier gene in FAP patients diagnosed with APC germline mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15761860
was generated by: ECO_0000203

NP54216.RAdA Q9mlpiF4dhk4U4X1OUBzNs-CQtenOUxM7Jh8Zjbo
has assertion: NP54216.RAdA Q9mlpiF4dhk4U4X1OUBzNs-CQtenOUxM7Jh8Zjbo130 assertion
has provenance: NP54216.RAdA Q9mlpiF4dhk4U4X1OUBzNs-CQtenOUxM7Jh8Zjbo130 provenance
has publication info: NP54216.RAdA Q9mlpiF4dhk4U4X1OUBzNs-CQtenOUxM7Jh8Zjbo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54216.RAdA Q9mlpiF4dhk4U4X1OUBzNs-CQtenOUxM7Jh8Zjbo130 assertion
type: Assertion
description: [These data extend the association of MUC7*5 allelic polymorphisms and asthma to inner-city African Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19820409
was generated by: ECO_0000203

NP54224.RAZ7CpvRBTEhHEXi45DUF-r65xMRmsuk5ynpWYGQPF yQ
has assertion: NP54224.RAZ7CpvRBTEhHEXi45DUF-r65xMRmsuk5ynpWYGQPF yQ130 assertion
has provenance: NP54224.RAZ7CpvRBTEhHEXi45DUF-r65xMRmsuk5ynpWYGQPF yQ130 provenance
has publication info: NP54224.RAZ7CpvRBTEhHEXi45DUF-r65xMRmsuk5ynpWYGQPF yQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54224.RAZ7CpvRBTEhHEXi45DUF-r65xMRmsuk5ynpWYGQPF yQ130 assertion
type: Assertion
description: [MTHFR, MTR, and MTRR polymorphisms in relation to p16INK4A hypermethylation in mucosa of patients with colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20549016
was generated by: ECO_0000203

NP54225.RAf5yTHlABPjNg0oEgShF9ieeXiP257O9gdhLrd9BwAPk
has assertion: NP54225.RAf5yTHlABPjNg0oEgShF9ieeXiP257O9gdhLrd9BwAPk130 assertion
has provenance: NP54225.RAf5yTHlABPjNg0oEgShF9ieeXiP257O9gdhLrd9BwAPk130 provenance
has publication info: NP54225.RAf5yTHlABPjNg0oEgShF9ieeXiP257O9gdhLrd9BwAPk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54225.RAf5yTHlABPjNg0oEgShF9ieeXiP257O9gdhLrd9BwAPk130 assertion
type: Assertion
description: [MTRR polymorphism interacted with the association of folate (P for interaction = 0.04) or vitamin (P for interaction = 0.02) with colorectal cancer, although the other polymorphisms did not interact with any nutrient intake.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16351505
was generated by: ECO_0000203

NP54226.RARU5eiP8BObTpXxWsl91Q3yRwPcHRams3NS0awcF56ko
has assertion: NP54226.RARU5eiP8BObTpXxWsl91Q3yRwPcHRams3NS0awcF56ko130 assertion
has provenance: NP54226.RARU5eiP8BObTpXxWsl91Q3yRwPcHRams3NS0awcF56ko130 provenance
has publication info: NP54226.RARU5eiP8BObTpXxWsl91Q3yRwPcHRams3NS0awcF56ko130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54226.RARU5eiP8BObTpXxWsl91Q3yRwPcHRams3NS0awcF56ko130 assertion
type: Assertion
description: [This population-based case-control study was designed to investigate the interrelationships between polymorphisms in the methylenetetrahydrofolate (MTHFR C677T and A1298C) gene and other genes (MTR A2756G; MTRR A66G and CBS 844ins68), intake of B-vitamins and colorectal cancer risk (CRC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12020105
was generated by: ECO_0000203

NP54229.RAZcEfZTAZSrb2SLpVWbuSrPxC5grfkPlF-PW6Iw7SO7k
has assertion: NP54229.RAZcEfZTAZSrb2SLpVWbuSrPxC5grfkPlF-PW6Iw7SO7k130 assertion
has provenance: NP54229.RAZcEfZTAZSrb2SLpVWbuSrPxC5grfkPlF-PW6Iw7SO7k130 provenance
has publication info: NP54229.RAZcEfZTAZSrb2SLpVWbuSrPxC5grfkPlF-PW6Iw7SO7k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54229.RAZcEfZTAZSrb2SLpVWbuSrPxC5grfkPlF-PW6Iw7SO7k130 assertion
type: Assertion
description: [The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20437058
was generated by: ECO_0000203

NP54230.RAV4tt-gOQ4y08R-lskXGmvP8eOT0dfF PvfaknqoMzqs
has assertion: NP54230.RAV4tt-gOQ4y08R-lskXGmvP8eOT0dfF PvfaknqoMzqs130 assertion
has provenance: NP54230.RAV4tt-gOQ4y08R-lskXGmvP8eOT0dfF PvfaknqoMzqs130 provenance
has publication info: NP54230.RAV4tt-gOQ4y08R-lskXGmvP8eOT0dfF PvfaknqoMzqs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54230.RAV4tt-gOQ4y08R-lskXGmvP8eOT0dfF PvfaknqoMzqs130 assertion
type: Assertion
description: [Germline polymorphisms in the one-carbon metabolism pathway and DNA methylation in colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19936946
was generated by: ECO_0000203

NP54234.RAdyu6mA2UrAQeo4VXToRHY5oD2oYkHgKFT3-iZUjJWL4
has assertion: NP54234.RAdyu6mA2UrAQeo4VXToRHY5oD2oYkHgKFT3-iZUjJWL4130 assertion
has provenance: NP54234.RAdyu6mA2UrAQeo4VXToRHY5oD2oYkHgKFT3-iZUjJWL4130 provenance
has publication info: NP54234.RAdyu6mA2UrAQeo4VXToRHY5oD2oYkHgKFT3-iZUjJWL4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54234.RAdyu6mA2UrAQeo4VXToRHY5oD2oYkHgKFT3-iZUjJWL4130 assertion
type: Assertion
description: [These results are consistent with accepted paradigms and offer a plausible explanation for the effect and interaction of specific SNPs in the TE phenotype. The biological implications of the limited number of MTHFR/MTHFR mutant alleles that can coexist, u]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12855226
was generated by: ECO_0000203

NP54235.RAeMqn5hL9ge172LqvkUkzY5khEWbQXjOVXyoYUhNGDCY
has assertion: NP54235.RAeMqn5hL9ge172LqvkUkzY5khEWbQXjOVXyoYUhNGDCY130 assertion
has provenance: NP54235.RAeMqn5hL9ge172LqvkUkzY5khEWbQXjOVXyoYUhNGDCY130 provenance
has publication info: NP54235.RAeMqn5hL9ge172LqvkUkzY5khEWbQXjOVXyoYUhNGDCY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54235.RAeMqn5hL9ge172LqvkUkzY5khEWbQXjOVXyoYUhNGDCY130 assertion
type: Assertion
description: [In a case-control study, we evaluated whether four common polymorphisms in methylenetetrahydrofolate reductase (MTHFR C677T and A1298C), methionine synthase (MS A2756G), and methionine synthase reductase (MTRR A66G) genes may have a role in altering susceptibility to adult acute lymphoblastic leukemia (ALL) and non-Hodgkin's lymphoma (NHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15159311
was generated by: ECO_0000203

NP54236.RAZZQVOF-9Mrb HRcSvcEzrwrZvEe8IIhouSmRIzOz97I
has assertion: NP54236.RAZZQVOF-9Mrb HRcSvcEzrwrZvEe8IIhouSmRIzOz97I130 assertion
has provenance: NP54236.RAZZQVOF-9Mrb HRcSvcEzrwrZvEe8IIhouSmRIzOz97I130 provenance
has publication info: NP54236.RAZZQVOF-9Mrb HRcSvcEzrwrZvEe8IIhouSmRIzOz97I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54236.RAZZQVOF-9Mrb HRcSvcEzrwrZvEe8IIhouSmRIzOz97I130 assertion
type: Assertion
description: [The double heterozygosity MTR 2756 AG/MTRR 66 AG was the single combined genotype that was a significant risk factor for having a DS child, with an OR estimated at 5.0 (95% CI: 1.1-24.1), after adjustment for t-Hcys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12923861
was generated by: ECO_0000203

NP54237.RASbq4apTaBVA0ruKsqzHFZZwWl3kUtMuiLIGWCNonGQ4
has assertion: NP54237.RASbq4apTaBVA0ruKsqzHFZZwWl3kUtMuiLIGWCNonGQ4130 assertion
has provenance: NP54237.RASbq4apTaBVA0ruKsqzHFZZwWl3kUtMuiLIGWCNonGQ4130 provenance
has publication info: NP54237.RASbq4apTaBVA0ruKsqzHFZZwWl3kUtMuiLIGWCNonGQ4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54237.RASbq4apTaBVA0ruKsqzHFZZwWl3kUtMuiLIGWCNonGQ4130 assertion
type: Assertion
description: [Recent evidence has suggested that 5,10-methylenetetrahydrofolate reductase (MTHFR) and/or methionine synthase reductase (MTRR) might contribute to the maternal risk of trisomy 21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16115349
was generated by: ECO_0000203

NP54239.RAXpaOKrYwoMWcb2GzBmTvJEzY5uMMi36bpZi83VU2MsM
has assertion: NP54239.RAXpaOKrYwoMWcb2GzBmTvJEzY5uMMi36bpZi83VU2MsM130 assertion
has provenance: NP54239.RAXpaOKrYwoMWcb2GzBmTvJEzY5uMMi36bpZi83VU2MsM130 provenance
has publication info: NP54239.RAXpaOKrYwoMWcb2GzBmTvJEzY5uMMi36bpZi83VU2MsM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54239.RAXpaOKrYwoMWcb2GzBmTvJEzY5uMMi36bpZi83VU2MsM130 assertion
type: Assertion
description: [As regards the MTRR A66G polymorphism, the presence of the mutated G allele either in the heterozygous or homozygous form was significantly more common among mothers of children with DS than among control subjects (odds ratio, 2.21; 95% CI, 1.11-4.40).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19254790
was generated by: ECO_0000203

NP54240.RARso0YBzYoGJsZtL8vp bOjnUIaV cl6nvKFmXjEqgv8
has assertion: NP54240.RARso0YBzYoGJsZtL8vp bOjnUIaV cl6nvKFmXjEqgv8130 assertion
has provenance: NP54240.RARso0YBzYoGJsZtL8vp bOjnUIaV cl6nvKFmXjEqgv8130 provenance
has publication info: NP54240.RARso0YBzYoGJsZtL8vp bOjnUIaV cl6nvKFmXjEqgv8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54240.RARso0YBzYoGJsZtL8vp bOjnUIaV cl6nvKFmXjEqgv8130 assertion
type: Assertion
description: [The increased risk of DS for homozygous RFC-1 80G>A was not associated with MTR 2756A>G. Positive interactions were found for the following genotype-pairs: MTHFR(CT+TT)/MTRR GG, MTHFR (CT+TT)/RFC-1 AA, MTHFR CC/MTR(AG+GG), MTHFR (CT+TT)/MTR AA, MTRR GG/MTR AA, and RFC-1 AA/MTRAA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20466634
was generated by: ECO_0000203

NP54242.RAR13Hp9sfDmjWK2c1LzTQtI1qVYBUIEoxsEfp8YOEfqQ
has assertion: NP54242.RAR13Hp9sfDmjWK2c1LzTQtI1qVYBUIEoxsEfp8YOEfqQ130 assertion
has provenance: NP54242.RAR13Hp9sfDmjWK2c1LzTQtI1qVYBUIEoxsEfp8YOEfqQ130 provenance
has publication info: NP54242.RAR13Hp9sfDmjWK2c1LzTQtI1qVYBUIEoxsEfp8YOEfqQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54242.RAR13Hp9sfDmjWK2c1LzTQtI1qVYBUIEoxsEfp8YOEfqQ130 assertion
type: Assertion
description: [Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in Brazil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15889417
was generated by: ECO_0000203

NP54243.RASHfcMGGvtU0nkMRK xfNIuv51FCYS2Dsf3cTSWMLa2I
has assertion: NP54243.RASHfcMGGvtU0nkMRK xfNIuv51FCYS2Dsf3cTSWMLa2I130 assertion
has provenance: NP54243.RASHfcMGGvtU0nkMRK xfNIuv51FCYS2Dsf3cTSWMLa2I130 provenance
has publication info: NP54243.RASHfcMGGvtU0nkMRK xfNIuv51FCYS2Dsf3cTSWMLa2I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54243.RASHfcMGGvtU0nkMRK xfNIuv51FCYS2Dsf3cTSWMLa2I130 assertion
type: Assertion
description: [Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR genes: is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16575899
was generated by: ECO_0000203

NP54245.RARW ODhSMheko WaOvdfUK2PrvnqX8-CEkJhmtjnWi4s
has assertion: NP54245.RARW ODhSMheko WaOvdfUK2PrvnqX8-CEkJhmtjnWi4s130 assertion
has provenance: NP54245.RARW ODhSMheko WaOvdfUK2PrvnqX8-CEkJhmtjnWi4s130 provenance
has publication info: NP54245.RARW ODhSMheko WaOvdfUK2PrvnqX8-CEkJhmtjnWi4s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54245.RARW ODhSMheko WaOvdfUK2PrvnqX8-CEkJhmtjnWi4s130 assertion
type: Assertion
description: [MTHFR and MTRR gene mutation alleles are related to Down syndrome, and CT, TT and GG gene mutation types increase the risk of Down syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18257130
was generated by: ECO_0000203

NP54250.RAWZ47hGQ v-QtYr2xXNOUxufb6ihbyzZ04jiDoQDhk7k
has assertion: NP54250.RAWZ47hGQ v-QtYr2xXNOUxufb6ihbyzZ04jiDoQDhk7k130 assertion
has provenance: NP54250.RAWZ47hGQ v-QtYr2xXNOUxufb6ihbyzZ04jiDoQDhk7k130 provenance
has publication info: NP54250.RAWZ47hGQ v-QtYr2xXNOUxufb6ihbyzZ04jiDoQDhk7k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54250.RAWZ47hGQ v-QtYr2xXNOUxufb6ihbyzZ04jiDoQDhk7k130 assertion
type: Assertion
description: [ Genetic variation in the MTP promoter is likely to be highly involved in the production of dyslipidemia in type 2 diabetic subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12775233
was generated by: ECO_0000203

NP54253.RAUQqD82S5YQYQfYUPgiUqn2w8Q3jXcI6xWDjR0iBKKXE
has assertion: NP54253.RAUQqD82S5YQYQfYUPgiUqn2w8Q3jXcI6xWDjR0iBKKXE130 assertion
has provenance: NP54253.RAUQqD82S5YQYQfYUPgiUqn2w8Q3jXcI6xWDjR0iBKKXE130 provenance
has publication info: NP54253.RAUQqD82S5YQYQfYUPgiUqn2w8Q3jXcI6xWDjR0iBKKXE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54253.RAUQqD82S5YQYQfYUPgiUqn2w8Q3jXcI6xWDjR0iBKKXE130 assertion
type: Assertion
description: [The polymorphism of MTNR1B located in 3'-untranslated region (rs 1562444) was selected for its higher rate of heterozygosity among other single nucleotide polymorphisms (SNPs) in both MTNR1A and MTNR1B genes and investigated in RA patients (n = 173) and healthy controls (n = 195) by polymerase chain reaction-restriction fragment length polymorphism assay using NlaIII restriction enzyme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16098099
was generated by: ECO_0000203

NP54254.RAWnvcehcrJX09JkrZVJ8 gm1C5x4mBnc5F7YFnfIWNg0
has assertion: NP54254.RAWnvcehcrJX09JkrZVJ8 gm1C5x4mBnc5F7YFnfIWNg0130 assertion
has provenance: NP54254.RAWnvcehcrJX09JkrZVJ8 gm1C5x4mBnc5F7YFnfIWNg0130 provenance
has publication info: NP54254.RAWnvcehcrJX09JkrZVJ8 gm1C5x4mBnc5F7YFnfIWNg0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54254.RAWnvcehcrJX09JkrZVJ8 gm1C5x4mBnc5F7YFnfIWNg0130 assertion
type: Assertion
description: [We conclude that the pathogenetic role of the MTHFR T677 allele in migraine is modulated by functional polymorphisms of TS and MTHFD1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15953655
was generated by: ECO_0000203

NP54256.RAaoLXwfOTaiXJoN 57ClZa2ttsbQxnNKF5fgwqgRon7g
has assertion: NP54256.RAaoLXwfOTaiXJoN 57ClZa2ttsbQxnNKF5fgwqgRon7g130 assertion
has provenance: NP54256.RAaoLXwfOTaiXJoN 57ClZa2ttsbQxnNKF5fgwqgRon7g130 provenance
has publication info: NP54256.RAaoLXwfOTaiXJoN 57ClZa2ttsbQxnNKF5fgwqgRon7g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54256.RAaoLXwfOTaiXJoN 57ClZa2ttsbQxnNKF5fgwqgRon7g130 assertion
type: Assertion
description: [The MTHFD1 R653Q, SLC19A1 R27H, and TCN2 P259R polymorphisms showed no significant association with omphalocele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15937947
was generated by: ECO_0000203

NP54257.RASu9y-lKtW6iajigBz7ds4a0TjqwO5F7-KuznlZEAhko
has assertion: NP54257.RASu9y-lKtW6iajigBz7ds4a0TjqwO5F7-KuznlZEAhko130 assertion
has provenance: NP54257.RASu9y-lKtW6iajigBz7ds4a0TjqwO5F7-KuznlZEAhko130 provenance
has publication info: NP54257.RASu9y-lKtW6iajigBz7ds4a0TjqwO5F7-KuznlZEAhko130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54257.RASu9y-lKtW6iajigBz7ds4a0TjqwO5F7-KuznlZEAhko130 assertion
type: Assertion
description: [In conclusion, polymorphisms in the folate-related genes MTHFR, MTRR, and SHMT1 are related to MTX resistance in pediatric ALL patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15797993
was generated by: ECO_0000203

NP54258.RAY6yyYQxVAdhibYdn5ko VNvaRRw82vkBbHqkVWs6BcM
has assertion: NP54258.RAY6yyYQxVAdhibYdn5ko VNvaRRw82vkBbHqkVWs6BcM130 assertion
has provenance: NP54258.RAY6yyYQxVAdhibYdn5ko VNvaRRw82vkBbHqkVWs6BcM130 provenance
has publication info: NP54258.RAY6yyYQxVAdhibYdn5ko VNvaRRw82vkBbHqkVWs6BcM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54258.RAY6yyYQxVAdhibYdn5ko VNvaRRw82vkBbHqkVWs6BcM130 assertion
type: Assertion
description: [We conclude that women who are 'QQ' homozygote for the MTHFD1 1258G --> A (R653Q) polymorphism are almost three times more likely to develop severe abruptio placentae during their pregnancy than women who are 'RQ' or 'RR.']. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15633187
was generated by: ECO_0000203

NP54266.RAZ2fX0K1VADUUZiUvItAKzRN84y4M0ewYvXKe8f5ffSM
has assertion: NP54266.RAZ2fX0K1VADUUZiUvItAKzRN84y4M0ewYvXKe8f5ffSM130 assertion
has provenance: NP54266.RAZ2fX0K1VADUUZiUvItAKzRN84y4M0ewYvXKe8f5ffSM130 provenance
has publication info: NP54266.RAZ2fX0K1VADUUZiUvItAKzRN84y4M0ewYvXKe8f5ffSM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54266.RAZ2fX0K1VADUUZiUvItAKzRN84y4M0ewYvXKe8f5ffSM130 assertion
type: Assertion
description: [Single and multivariate associations of MSR1, ELAC2, and RNASEL with prostate cancer in an ethnic diverse cohort of men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20086112
was generated by: ECO_0000203

NP54267.RAVHjMV1--onklIgxoLH96Gk3LoysnrrVVxhijTdt3ImE
has assertion: NP54267.RAVHjMV1--onklIgxoLH96Gk3LoysnrrVVxhijTdt3ImE130 assertion
has provenance: NP54267.RAVHjMV1--onklIgxoLH96Gk3LoysnrrVVxhijTdt3ImE130 provenance
has publication info: NP54267.RAVHjMV1--onklIgxoLH96Gk3LoysnrrVVxhijTdt3ImE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54267.RAVHjMV1--onklIgxoLH96Gk3LoysnrrVVxhijTdt3ImE130 assertion
type: Assertion
description: [Joint effects of inflammation and androgen metabolism on prostate cancer severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18566991
was generated by: ECO_0000203

NP54273.RAd7jslrZFYeKNh3Jn3iSfzxVkTfbCAz6EPtZY-BaBABY
has assertion: NP54273.RAd7jslrZFYeKNh3Jn3iSfzxVkTfbCAz6EPtZY-BaBABY130 assertion
has provenance: NP54273.RAd7jslrZFYeKNh3Jn3iSfzxVkTfbCAz6EPtZY-BaBABY130 provenance
has publication info: NP54273.RAd7jslrZFYeKNh3Jn3iSfzxVkTfbCAz6EPtZY-BaBABY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54273.RAd7jslrZFYeKNh3Jn3iSfzxVkTfbCAz6EPtZY-BaBABY130 assertion
type: Assertion
description: [We genotyped 929 CRC patients and 1098 control subjects from Ontario, and 467 patients and 344 controls from Newfoundland and Labrador, for two promoter polymorphisms in the MMR genes MSH2 and MSH6 using the fluorogenic 5' nuclease assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17942459
was generated by: ECO_0000203

NP54277.RAW3KZDnKYLKWMcysemxN3rNyAvJxFm-Isam RU8Hqjc8
has assertion: NP54277.RAW3KZDnKYLKWMcysemxN3rNyAvJxFm-Isam RU8Hqjc8130 assertion
has provenance: NP54277.RAW3KZDnKYLKWMcysemxN3rNyAvJxFm-Isam RU8Hqjc8130 provenance
has publication info: NP54277.RAW3KZDnKYLKWMcysemxN3rNyAvJxFm-Isam RU8Hqjc8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54277.RAW3KZDnKYLKWMcysemxN3rNyAvJxFm-Isam RU8Hqjc8130 assertion
type: Assertion
description: [Single nucleotide polymorphism analysis of germline MSH6 gene mutations in Chinese hereditary non-polyposis colorectal cancer probands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19173809
was generated by: ECO_0000203

NP54279.RAdIDTmvsIwgPkaV0yUc0URDq35nSSg P KDUh7XR9pGE
has assertion: NP54279.RAdIDTmvsIwgPkaV0yUc0URDq35nSSg P KDUh7XR9pGE130 assertion
has provenance: NP54279.RAdIDTmvsIwgPkaV0yUc0URDq35nSSg P KDUh7XR9pGE130 provenance
has publication info: NP54279.RAdIDTmvsIwgPkaV0yUc0URDq35nSSg P KDUh7XR9pGE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54279.RAdIDTmvsIwgPkaV0yUc0URDq35nSSg P KDUh7XR9pGE130 assertion
type: Assertion
description: [Screening for germline mutations of MLH1, MSH2, MSH6 and PMS2 genes in Slovenian colorectal cancer patients: implications for a population specific detection strategy of Lynch syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19526325
was generated by: ECO_0000203

NP54284.RAVoTGhrrnmTdL6fsfRw0KDU EesMa6OPPdF06z2TQfU0
has assertion: NP54284.RAVoTGhrrnmTdL6fsfRw0KDU EesMa6OPPdF06z2TQfU0130 assertion
has provenance: NP54284.RAVoTGhrrnmTdL6fsfRw0KDU EesMa6OPPdF06z2TQfU0130 provenance
has publication info: NP54284.RAVoTGhrrnmTdL6fsfRw0KDU EesMa6OPPdF06z2TQfU0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54284.RAVoTGhrrnmTdL6fsfRw0KDU EesMa6OPPdF06z2TQfU0130 assertion
type: Assertion
description: [Median age at diagnosis of first CRC in MSH6 mutation families was 59 years compared to 45 years in both MLH1 and MSH2 mutation families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17939062
was generated by: ECO_0000203

NP54287.RAbHPvDSCRbj9Bvo8ROkdAJ VzZYXpg2hFAifHqLtcIFM
has assertion: NP54287.RAbHPvDSCRbj9Bvo8ROkdAJ VzZYXpg2hFAifHqLtcIFM130 assertion
has provenance: NP54287.RAbHPvDSCRbj9Bvo8ROkdAJ VzZYXpg2hFAifHqLtcIFM130 provenance
has publication info: NP54287.RAbHPvDSCRbj9Bvo8ROkdAJ VzZYXpg2hFAifHqLtcIFM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54287.RAbHPvDSCRbj9Bvo8ROkdAJ VzZYXpg2hFAifHqLtcIFM130 assertion
type: Assertion
description: [Genetic investigation of DNA repair genes PMS2, MLH1, MSH2, MSH6, MUTYH, OGG1 and MTH1, as possible susceptibility factors for sporadic CRC, was done using both a haplotype tagging and a candidate (i.e.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17417778
was generated by: ECO_0000203

NP54295.RAd0XbB 5NKRAnpvE92Wi-ypPEoMotMwXAdV-Vd-1BfSU
has assertion: NP54295.RAd0XbB 5NKRAnpvE92Wi-ypPEoMotMwXAdV-Vd-1BfSU130 assertion
has provenance: NP54295.RAd0XbB 5NKRAnpvE92Wi-ypPEoMotMwXAdV-Vd-1BfSU130 provenance
has publication info: NP54295.RAd0XbB 5NKRAnpvE92Wi-ypPEoMotMwXAdV-Vd-1BfSU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54295.RAd0XbB 5NKRAnpvE92Wi-ypPEoMotMwXAdV-Vd-1BfSU130 assertion
type: Assertion
description: [in central Ohio, at least 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16885385
was generated by: ECO_0000203

NP54299.RATuxXPBsVDR73a4Ljzc9qnR- wu8ddhLknC IG8z59PE
has assertion: NP54299.RATuxXPBsVDR73a4Ljzc9qnR- wu8ddhLknC IG8z59PE130 assertion
has provenance: NP54299.RATuxXPBsVDR73a4Ljzc9qnR- wu8ddhLknC IG8z59PE130 provenance
has publication info: NP54299.RATuxXPBsVDR73a4Ljzc9qnR- wu8ddhLknC IG8z59PE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54299.RATuxXPBsVDR73a4Ljzc9qnR- wu8ddhLknC IG8z59PE130 assertion
type: Assertion
description: [These results suggest that the polymorphism may be associated with an increased risk to develop NHL and that probably there are differences in the effect of the polymorphisms among populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11890986
was generated by: ECO_0000203

NP54308.RAaPVJeJnp3ae14jzIxkPOsVglYX13rBO1Tq26prr9bNs
has assertion: NP54308.RAaPVJeJnp3ae14jzIxkPOsVglYX13rBO1Tq26prr9bNs130 assertion
has provenance: NP54308.RAaPVJeJnp3ae14jzIxkPOsVglYX13rBO1Tq26prr9bNs130 provenance
has publication info: NP54308.RAaPVJeJnp3ae14jzIxkPOsVglYX13rBO1Tq26prr9bNs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54308.RAaPVJeJnp3ae14jzIxkPOsVglYX13rBO1Tq26prr9bNs130 assertion
type: Assertion
description: [Our results demonstrate ethnic differences in polymorphisms of atopy candidate genes. Additional studies involving larger samples are required to investigate the association between asthma or atopy and the genotypes studied to date in Chinese children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12422339
was generated by: ECO_0000203

NP54309.RAYcjMmRDezJ1iWGu6BQszKLNhRC Uq3Ajt jqJVLO5LA
has assertion: NP54309.RAYcjMmRDezJ1iWGu6BQszKLNhRC Uq3Ajt jqJVLO5LA130 assertion
has provenance: NP54309.RAYcjMmRDezJ1iWGu6BQszKLNhRC Uq3Ajt jqJVLO5LA130 provenance
has publication info: NP54309.RAYcjMmRDezJ1iWGu6BQszKLNhRC Uq3Ajt jqJVLO5LA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54309.RAYcjMmRDezJ1iWGu6BQszKLNhRC Uq3Ajt jqJVLO5LA130 assertion
type: Assertion
description: [ These results show the FcgammaRIIa-R131 allele to be associated with periodontitis risk in SLE patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12710759
was generated by: ECO_0000203

NP54310.RAYgeiaveMi8vW4Q-ZaqA-am2lEFl0MWOO-GU Q2hygI0
has assertion: NP54310.RAYgeiaveMi8vW4Q-ZaqA-am2lEFl0MWOO-GU Q2hygI0130 assertion
has provenance: NP54310.RAYgeiaveMi8vW4Q-ZaqA-am2lEFl0MWOO-GU Q2hygI0130 provenance
has publication info: NP54310.RAYgeiaveMi8vW4Q-ZaqA-am2lEFl0MWOO-GU Q2hygI0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54310.RAYgeiaveMi8vW4Q-ZaqA-am2lEFl0MWOO-GU Q2hygI0130 assertion
type: Assertion
description: [ This study supports the notion that polymorphisms in the Fc epsilon R1-beta gene have significant effects on IgE responsiveness. Secondly, dust mites in rural populations influence the expression of genes on chromosome 11q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12047428
was generated by: ECO_0000203

NP54319.RAVoQ8I-VTRlVoGEtQrkZ-Je2IlJolrgrCNjIyqNNHubI
has assertion: NP54319.RAVoQ8I-VTRlVoGEtQrkZ-Je2IlJolrgrCNjIyqNNHubI130 assertion
has provenance: NP54319.RAVoQ8I-VTRlVoGEtQrkZ-Je2IlJolrgrCNjIyqNNHubI130 provenance
has publication info: NP54319.RAVoQ8I-VTRlVoGEtQrkZ-Je2IlJolrgrCNjIyqNNHubI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54319.RAVoQ8I-VTRlVoGEtQrkZ-Je2IlJolrgrCNjIyqNNHubI130 assertion
type: Assertion
description: [ Our findings suggest that promoter polymorphisms of both CTLA4 and FCER1B are genetic factors that influence total serum IgE levels in patients with asthma. This supports the theory that variance in total serum IgE levels in patients with asthma is determined by mutations in multiple genes, each of which has a relatively small effect on the phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11447385
was generated by: ECO_0000203

NP54324.RAfYYNiwDKRZj CfqUdNNj0xZuJrR3F4AMbDAEWoygmI0
has assertion: NP54324.RAfYYNiwDKRZj CfqUdNNj0xZuJrR3F4AMbDAEWoygmI0130 assertion
has provenance: NP54324.RAfYYNiwDKRZj CfqUdNNj0xZuJrR3F4AMbDAEWoygmI0130 provenance
has publication info: NP54324.RAfYYNiwDKRZj CfqUdNNj0xZuJrR3F4AMbDAEWoygmI0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54324.RAfYYNiwDKRZj CfqUdNNj0xZuJrR3F4AMbDAEWoygmI0130 assertion
type: Assertion
description: [An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11080237
was generated by: ECO_0000203

NP54329.RAXvfxLJeHEWUJcY7-k0ocP7NsBHTbJpYYRuoKRDsTQ6U
has assertion: NP54329.RAXvfxLJeHEWUJcY7-k0ocP7NsBHTbJpYYRuoKRDsTQ6U130 assertion
has provenance: NP54329.RAXvfxLJeHEWUJcY7-k0ocP7NsBHTbJpYYRuoKRDsTQ6U130 provenance
has publication info: NP54329.RAXvfxLJeHEWUJcY7-k0ocP7NsBHTbJpYYRuoKRDsTQ6U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54329.RAXvfxLJeHEWUJcY7-k0ocP7NsBHTbJpYYRuoKRDsTQ6U130 assertion
type: Assertion
description: [Common genetic variants in the interleukin-6 and chitotriosidase genes are associated with the risk for serious infection in children undergoing therapy for acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16107886
was generated by: ECO_0000203

NP54331.RAe2tVER SS4DVHDbAawTxjLYIC foaoTp8W07WBOyQPU
has assertion: NP54331.RAe2tVER SS4DVHDbAawTxjLYIC foaoTp8W07WBOyQPU130 assertion
has provenance: NP54331.RAe2tVER SS4DVHDbAawTxjLYIC foaoTp8W07WBOyQPU130 provenance
has publication info: NP54331.RAe2tVER SS4DVHDbAawTxjLYIC foaoTp8W07WBOyQPU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54331.RAe2tVER SS4DVHDbAawTxjLYIC foaoTp8W07WBOyQPU130 assertion
type: Assertion
description: [A polymorphism in the promoter region of myeloperoxidase (463G-->A) has been found to be inversely associated with lung cancer; differences in the association with age and gender have been suggested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17304047
was generated by: ECO_0000203

NP54339.RAYtzYjr9ahbFynl43VuFSmimkHbI9ti6QdEaD-ewGRzI
has assertion: NP54339.RAYtzYjr9ahbFynl43VuFSmimkHbI9ti6QdEaD-ewGRzI130 assertion
has provenance: NP54339.RAYtzYjr9ahbFynl43VuFSmimkHbI9ti6QdEaD-ewGRzI130 provenance
has publication info: NP54339.RAYtzYjr9ahbFynl43VuFSmimkHbI9ti6QdEaD-ewGRzI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54339.RAYtzYjr9ahbFynl43VuFSmimkHbI9ti6QdEaD-ewGRzI130 assertion
type: Assertion
description: [Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early-onset lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20091863
was generated by: ECO_0000203

NP54345.RARdRNGK71AYUfJ xHV7m0fCmvY4AGHtZ9J7HqNTLYMCw
has assertion: NP54345.RARdRNGK71AYUfJ xHV7m0fCmvY4AGHtZ9J7HqNTLYMCw130 assertion
has provenance: NP54345.RARdRNGK71AYUfJ xHV7m0fCmvY4AGHtZ9J7HqNTLYMCw130 provenance
has publication info: NP54345.RARdRNGK71AYUfJ xHV7m0fCmvY4AGHtZ9J7HqNTLYMCw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54345.RARdRNGK71AYUfJ xHV7m0fCmvY4AGHtZ9J7HqNTLYMCw130 assertion
type: Assertion
description: [We investigated the prognostic significance of genetic polymorphism in glutathione-S transferase mu 1 (GSTM1), glutathione-S transferase theta 1 (GSTT1), NAD(P)H:quinone oxidoreductase (NQO1) and myeloperoxidase (MPO), the products of which are associated with drug metabolism as well as with detoxication, in 193 patients with de novo acute myeloid leukemia (AML) other than M3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11840286
was generated by: ECO_0000203

NP54353.RAcxfLDFUWI5hrjMFFtBMgdQ1ynhvA49uhCtKMPa11S4Y
has assertion: NP54353.RAcxfLDFUWI5hrjMFFtBMgdQ1ynhvA49uhCtKMPa11S4Y130 assertion
has provenance: NP54353.RAcxfLDFUWI5hrjMFFtBMgdQ1ynhvA49uhCtKMPa11S4Y130 provenance
has publication info: NP54353.RAcxfLDFUWI5hrjMFFtBMgdQ1ynhvA49uhCtKMPa11S4Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54353.RAcxfLDFUWI5hrjMFFtBMgdQ1ynhvA49uhCtKMPa11S4Y130 assertion
type: Assertion
description: [These findings suggest that individual susceptibility of bladder cancer may be modulated by MPO and MnSOD polymorphisms, and that the combination of genetic factors involved in oxidative stress response with environmental carcinogens may play an important role in bladder carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14729580
was generated by: ECO_0000203

NP54356.RAVtf9m5rxZO3U8udN72EmKxP6sXxFdUTyawB4Ev95fzM
has assertion: NP54356.RAVtf9m5rxZO3U8udN72EmKxP6sXxFdUTyawB4Ev95fzM130 assertion
has provenance: NP54356.RAVtf9m5rxZO3U8udN72EmKxP6sXxFdUTyawB4Ev95fzM130 provenance
has publication info: NP54356.RAVtf9m5rxZO3U8udN72EmKxP6sXxFdUTyawB4Ev95fzM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54356.RAVtf9m5rxZO3U8udN72EmKxP6sXxFdUTyawB4Ev95fzM130 assertion
type: Assertion
description: [Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19692168
was generated by: ECO_0000203

NP54358.RAbtxSU-da6vpealL8KF-pu91OyeSnkGpJ7WAUIKjeQm0
has assertion: NP54358.RAbtxSU-da6vpealL8KF-pu91OyeSnkGpJ7WAUIKjeQm0130 assertion
has provenance: NP54358.RAbtxSU-da6vpealL8KF-pu91OyeSnkGpJ7WAUIKjeQm0130 provenance
has publication info: NP54358.RAbtxSU-da6vpealL8KF-pu91OyeSnkGpJ7WAUIKjeQm0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54358.RAbtxSU-da6vpealL8KF-pu91OyeSnkGpJ7WAUIKjeQm0130 assertion
type: Assertion
description: [Neither the MPO mutation nor specific genotypes of cytochrome P4502D6 were associated with CA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11147929
was generated by: ECO_0000203

NP54365.RAfOcpE6PaBQa6ybAl2VNo IK7pTQLQ6LcpsHzixndksM
has assertion: NP54365.RAfOcpE6PaBQa6ybAl2VNo IK7pTQLQ6LcpsHzixndksM130 assertion
has provenance: NP54365.RAfOcpE6PaBQa6ybAl2VNo IK7pTQLQ6LcpsHzixndksM130 provenance
has publication info: NP54365.RAfOcpE6PaBQa6ybAl2VNo IK7pTQLQ6LcpsHzixndksM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54365.RAfOcpE6PaBQa6ybAl2VNo IK7pTQLQ6LcpsHzixndksM130 assertion
type: Assertion
description: [These data indicate that gene variants that impact oxidative stress modify prognosis after treatment for breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15705913
was generated by: ECO_0000203

NP54367.RAZdLXPGxHaqMfHXuPORJMPkj-7PeD4B3DrSyR 0sgAzM
has assertion: NP54367.RAZdLXPGxHaqMfHXuPORJMPkj-7PeD4B3DrSyR 0sgAzM130 assertion
has provenance: NP54367.RAZdLXPGxHaqMfHXuPORJMPkj-7PeD4B3DrSyR 0sgAzM130 provenance
has publication info: NP54367.RAZdLXPGxHaqMfHXuPORJMPkj-7PeD4B3DrSyR 0sgAzM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54367.RAZdLXPGxHaqMfHXuPORJMPkj-7PeD4B3DrSyR 0sgAzM130 assertion
type: Assertion
description: [from this study suggest that exogenous and endogenous modulators of oxidative stress may modify the association between the MPO polymorphism and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18340529
was generated by: ECO_0000203

NP54371.RAQjTW4YRWYJ7V8nYbUDFq5MrZEp8zDfRQ0vqtmlJ-KHw
has assertion: NP54371.RAQjTW4YRWYJ7V8nYbUDFq5MrZEp8zDfRQ0vqtmlJ-KHw130 assertion
has provenance: NP54371.RAQjTW4YRWYJ7V8nYbUDFq5MrZEp8zDfRQ0vqtmlJ-KHw130 provenance
has publication info: NP54371.RAQjTW4YRWYJ7V8nYbUDFq5MrZEp8zDfRQ0vqtmlJ-KHw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54371.RAQjTW4YRWYJ7V8nYbUDFq5MrZEp8zDfRQ0vqtmlJ-KHw130 assertion
type: Assertion
description: [We assessed 27 selected polymorphisms based on previously described associations or putative functional effects in 16 key genes from pathways that may influence cellular sensitivity to taxanes (ABCB1, ABCC1, ABCC2, ABCG2, CDKN1A, CYP1B1, CYP2C8, CYP3A4, CYP3A5, MAPT, and TP53) and platinum (ABCC2, ABCG2, ERCC1, ERCC2, GSTP1, MPO, and XRCC1) using polymerase chain reaction and Pyrosequencing in 914 ovarian cancer patients from the Scottish Randomised Trial in Ovarian Cancer phase III trial who were treated at presentation with carboplatin and taxane regimens after cytoreductive surgery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17925548
was generated by: ECO_0000203

NP54374.RAdJCzmGqXTxeKAhqeAE7NIZXpfGdokjUWX C2abs4MiU
has assertion: NP54374.RAdJCzmGqXTxeKAhqeAE7NIZXpfGdokjUWX C2abs4MiU130 assertion
has provenance: NP54374.RAdJCzmGqXTxeKAhqeAE7NIZXpfGdokjUWX C2abs4MiU130 provenance
has publication info: NP54374.RAdJCzmGqXTxeKAhqeAE7NIZXpfGdokjUWX C2abs4MiU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54374.RAdJCzmGqXTxeKAhqeAE7NIZXpfGdokjUWX C2abs4MiU130 assertion
type: Assertion
description: [A functional variant of the myeloperoxidase gene is associated with cardiovascular disease in end-stage renal disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12694338
was generated by: ECO_0000203

NP54384.RAf6p9APUXo5ObYpc UXX8xduxLdK39u1pd3qHwUWnTx8
has assertion: NP54384.RAf6p9APUXo5ObYpc UXX8xduxLdK39u1pd3qHwUWnTx8130 assertion
has provenance: NP54384.RAf6p9APUXo5ObYpc UXX8xduxLdK39u1pd3qHwUWnTx8130 provenance
has publication info: NP54384.RAf6p9APUXo5ObYpc UXX8xduxLdK39u1pd3qHwUWnTx8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54384.RAf6p9APUXo5ObYpc UXX8xduxLdK39u1pd3qHwUWnTx8130 assertion
type: Assertion
description: [Genetic polymorphism in myeloperoxidase but not GSTM1 is associated with risk of lung squamous cell carcinoma in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12397651
was generated by: ECO_0000203

NP54385.RAVq o-3NAugVy2PZcJizd2quh61feHuDdvR4BQENXOAE
has assertion: NP54385.RAVq o-3NAugVy2PZcJizd2quh61feHuDdvR4BQENXOAE130 assertion
has provenance: NP54385.RAVq o-3NAugVy2PZcJizd2quh61feHuDdvR4BQENXOAE130 provenance
has publication info: NP54385.RAVq o-3NAugVy2PZcJizd2quh61feHuDdvR4BQENXOAE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54385.RAVq o-3NAugVy2PZcJizd2quh61feHuDdvR4BQENXOAE130 assertion
type: Assertion
description: [Polymorphisms of DNA repair genes and risk of non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16195237
was generated by: ECO_0000203

NP54391.RAcVNbZGiiIDUIeyrkVnOiDTaxmb2gY4g F3CRl8Wgv0s
has assertion: NP54391.RAcVNbZGiiIDUIeyrkVnOiDTaxmb2gY4g F3CRl8Wgv0s130 assertion
has provenance: NP54391.RAcVNbZGiiIDUIeyrkVnOiDTaxmb2gY4g F3CRl8Wgv0s130 provenance
has publication info: NP54391.RAcVNbZGiiIDUIeyrkVnOiDTaxmb2gY4g F3CRl8Wgv0s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54391.RAcVNbZGiiIDUIeyrkVnOiDTaxmb2gY4g F3CRl8Wgv0s130 assertion
type: Assertion
description: [have been difficult to draw and are partly hampered by the small number of patients in each study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20302034
was generated by: ECO_0000203

NP54393.RAbneBp6GEV---bo6Fg3shtLkkNk2lDEQMMKW56HJ dXI
has assertion: NP54393.RAbneBp6GEV---bo6Fg3shtLkkNk2lDEQMMKW56HJ dXI130 assertion
has provenance: NP54393.RAbneBp6GEV---bo6Fg3shtLkkNk2lDEQMMKW56HJ dXI130 provenance
has publication info: NP54393.RAbneBp6GEV---bo6Fg3shtLkkNk2lDEQMMKW56HJ dXI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54393.RAbneBp6GEV---bo6Fg3shtLkkNk2lDEQMMKW56HJ dXI130 assertion
type: Assertion
description: [Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12082592
was generated by: ECO_0000203

NP54398.RAYYAErn-0XORmHIycWVeXvezKlbi nxolwnFl610pzto
has assertion: NP54398.RAYYAErn-0XORmHIycWVeXvezKlbi nxolwnFl610pzto130 assertion
has provenance: NP54398.RAYYAErn-0XORmHIycWVeXvezKlbi nxolwnFl610pzto130 provenance
has publication info: NP54398.RAYYAErn-0XORmHIycWVeXvezKlbi nxolwnFl610pzto130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54398.RAYYAErn-0XORmHIycWVeXvezKlbi nxolwnFl610pzto130 assertion
type: Assertion
description: [Matrix metalloproteinase gene polymorphisms in patients with rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19504098
was generated by: ECO_0000203

NP54399.RAR6FrG0DOASTlsSFTLJurP3je4yxGVDgNOSql9qgV9 Y
has assertion: NP54399.RAR6FrG0DOASTlsSFTLJurP3je4yxGVDgNOSql9qgV9 Y130 assertion
has provenance: NP54399.RAR6FrG0DOASTlsSFTLJurP3je4yxGVDgNOSql9qgV9 Y130 provenance
has publication info: NP54399.RAR6FrG0DOASTlsSFTLJurP3je4yxGVDgNOSql9qgV9 Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54399.RAR6FrG0DOASTlsSFTLJurP3je4yxGVDgNOSql9qgV9 Y130 assertion
type: Assertion
description: [Thus, genetic polymorphisms may be associated with subsequent myocardial infarction, and may also be associated with treatment-associated bleeding among coronary patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12082590
was generated by: ECO_0000203

NP54401.RAdCi-lViTMQLwTy4-nQwPjY3U1AxLNjdRGBNn4LCddPI
has assertion: NP54401.RAdCi-lViTMQLwTy4-nQwPjY3U1AxLNjdRGBNn4LCddPI130 assertion
has provenance: NP54401.RAdCi-lViTMQLwTy4-nQwPjY3U1AxLNjdRGBNn4LCddPI130 provenance
has publication info: NP54401.RAdCi-lViTMQLwTy4-nQwPjY3U1AxLNjdRGBNn4LCddPI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54401.RAdCi-lViTMQLwTy4-nQwPjY3U1AxLNjdRGBNn4LCddPI130 assertion
type: Assertion
description: [In conclusion, our study in a large series of angiographically defined patients suggests that the C-1562T polymorphism may not be useful as a predictor of the presence and severity of coronary atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11410119
was generated by: ECO_0000203

NP54402.RASfEGFhbcHJaMwix9dWKz4i5M42rMA2dJCIXRKm-d3xE
has assertion: NP54402.RASfEGFhbcHJaMwix9dWKz4i5M42rMA2dJCIXRKm-d3xE130 assertion
has provenance: NP54402.RASfEGFhbcHJaMwix9dWKz4i5M42rMA2dJCIXRKm-d3xE130 provenance
has publication info: NP54402.RASfEGFhbcHJaMwix9dWKz4i5M42rMA2dJCIXRKm-d3xE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54402.RASfEGFhbcHJaMwix9dWKz4i5M42rMA2dJCIXRKm-d3xE130 assertion
type: Assertion
description: [No significant difference between controls and ACS patients was found in the frequencies of MMP-9 C-1562T and G5564A, Fib Bbeta-148C/T and GPVI T13254C genotypes and alleles (P > 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16080811
was generated by: ECO_0000203

NP54403.RASPAiPcmgFiOo8ELVD88q6oOhsYeeE5 A9m5bylrqRTM
has assertion: NP54403.RASPAiPcmgFiOo8ELVD88q6oOhsYeeE5 A9m5bylrqRTM130 assertion
has provenance: NP54403.RASPAiPcmgFiOo8ELVD88q6oOhsYeeE5 A9m5bylrqRTM130 provenance
has publication info: NP54403.RASPAiPcmgFiOo8ELVD88q6oOhsYeeE5 A9m5bylrqRTM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54403.RASPAiPcmgFiOo8ELVD88q6oOhsYeeE5 A9m5bylrqRTM130 assertion
type: Assertion
description: [The present findings suggest that the genetic polymorphism in MMP-9 promoter (C-1562-T) is associated with the susceptibility to ACS in the Han population of China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15952124
was generated by: ECO_0000203

NP54404.RAQKW3LzzWf0Q4JPO5Aj4199iuVoEaHsYkHXnTwrMWS0g
has assertion: NP54404.RAQKW3LzzWf0Q4JPO5Aj4199iuVoEaHsYkHXnTwrMWS0g130 assertion
has provenance: NP54404.RAQKW3LzzWf0Q4JPO5Aj4199iuVoEaHsYkHXnTwrMWS0g130 provenance
has publication info: NP54404.RAQKW3LzzWf0Q4JPO5Aj4199iuVoEaHsYkHXnTwrMWS0g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54404.RAQKW3LzzWf0Q4JPO5Aj4199iuVoEaHsYkHXnTwrMWS0g130 assertion
type: Assertion
description: [Our results show that functional genetic variation of stromelysin-1 could be a significant risk factor for stable angina, and might play an important role in coronary atherosclerosis involving vascular remodeling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12205736
was generated by: ECO_0000203

NP54407.RAfRUJ-1C28EE Hgqz9Kh59gdjTw310WJiAFDVvuIZ9wo
has assertion: NP54407.RAfRUJ-1C28EE Hgqz9Kh59gdjTw310WJiAFDVvuIZ9wo130 assertion
has provenance: NP54407.RAfRUJ-1C28EE Hgqz9Kh59gdjTw310WJiAFDVvuIZ9wo130 provenance
has publication info: NP54407.RAfRUJ-1C28EE Hgqz9Kh59gdjTw310WJiAFDVvuIZ9wo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54407.RAfRUJ-1C28EE Hgqz9Kh59gdjTw310WJiAFDVvuIZ9wo130 assertion
type: Assertion
description: [ Our results indicate that the T allele in the MMP-9 promoter is associated with the invasive phenotype of gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15565457
was generated by: ECO_0000203

NP54410.RAdZ-qmqrBMR0TKIu9OhICUV2hX VnltbxNE9mQtU20vU
has assertion: NP54410.RAdZ-qmqrBMR0TKIu9OhICUV2hX VnltbxNE9mQtU20vU130 assertion
has provenance: NP54410.RAdZ-qmqrBMR0TKIu9OhICUV2hX VnltbxNE9mQtU20vU130 provenance
has publication info: NP54410.RAdZ-qmqrBMR0TKIu9OhICUV2hX VnltbxNE9mQtU20vU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54410.RAdZ-qmqrBMR0TKIu9OhICUV2hX VnltbxNE9mQtU20vU130 assertion
type: Assertion
description: [In a prospective study of 1127 patients with documented coronary artery disease, we measured baseline plasma MMP-9 levels and determined the MMP-9/C-1562T and MMP-9/R279Q genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12668489
was generated by: ECO_0000203

NP54411.RAdZlVIhQWrfwJs79cCE8fSvFd7M oQ8ejrt KRcQrxw8
has assertion: NP54411.RAdZlVIhQWrfwJs79cCE8fSvFd7M oQ8ejrt KRcQrxw8130 assertion
has provenance: NP54411.RAdZlVIhQWrfwJs79cCE8fSvFd7M oQ8ejrt KRcQrxw8130 provenance
has publication info: NP54411.RAdZlVIhQWrfwJs79cCE8fSvFd7M oQ8ejrt KRcQrxw8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54411.RAdZlVIhQWrfwJs79cCE8fSvFd7M oQ8ejrt KRcQrxw8130 assertion
type: Assertion
description: [Matrix metalloproteinase-9 (MMP-9) plays an important role in the pathogenesis of atherosclerosis, the pathology underlying the majority of coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12728308
was generated by: ECO_0000203

NP54417.RAaj3tAfwpwckkLfk--nPELevYu6lDikfd82OwrTsuJ64
has assertion: NP54417.RAaj3tAfwpwckkLfk--nPELevYu6lDikfd82OwrTsuJ64130 assertion
has provenance: NP54417.RAaj3tAfwpwckkLfk--nPELevYu6lDikfd82OwrTsuJ64130 provenance
has publication info: NP54417.RAaj3tAfwpwckkLfk--nPELevYu6lDikfd82OwrTsuJ64130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54417.RAaj3tAfwpwckkLfk--nPELevYu6lDikfd82OwrTsuJ64130 assertion
type: Assertion
description: [Matrix metalloproteinase-9 genotypes and haplotypes are associated with multiple sclerosis and with the degree of disability of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19631393
was generated by: ECO_0000203

NP54428.RAZrQJHpxWf8slOnDenWxQeJAnaQXeIDURu5EK5DXAo0c
has assertion: NP54428.RAZrQJHpxWf8slOnDenWxQeJAnaQXeIDURu5EK5DXAo0c130 assertion
has provenance: NP54428.RAZrQJHpxWf8slOnDenWxQeJAnaQXeIDURu5EK5DXAo0c130 provenance
has publication info: NP54428.RAZrQJHpxWf8slOnDenWxQeJAnaQXeIDURu5EK5DXAo0c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54428.RAZrQJHpxWf8slOnDenWxQeJAnaQXeIDURu5EK5DXAo0c130 assertion
type: Assertion
description: [MMP-9 microsatellite polymorphism: association with the progression of intima-media thickening and constrictive remodeling of carotid atherosclerotic plaques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16159601
was generated by: ECO_0000203

NP54431.RAYHjsTS DqgcbbandXQgR2zR3gms 1SqvAqXqeSIVGI4
has assertion: NP54431.RAYHjsTS DqgcbbandXQgR2zR3gms 1SqvAqXqeSIVGI4130 assertion
has provenance: NP54431.RAYHjsTS DqgcbbandXQgR2zR3gms 1SqvAqXqeSIVGI4130 provenance
has publication info: NP54431.RAYHjsTS DqgcbbandXQgR2zR3gms 1SqvAqXqeSIVGI4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54431.RAYHjsTS DqgcbbandXQgR2zR3gms 1SqvAqXqeSIVGI4130 assertion
type: Assertion
description: [this study identified SNPs in MMP1, MMP2, MMP7 and MMP12 for further investigation as possible predictors of chemotherapy outcome in lung cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19643940
was generated by: ECO_0000203

NP54432.RAUNXxIcVbpIf YlDULFN1klTuAVfkTnOPm6RvagtIke0
has assertion: NP54432.RAUNXxIcVbpIf YlDULFN1klTuAVfkTnOPm6RvagtIke0130 assertion
has provenance: NP54432.RAUNXxIcVbpIf YlDULFN1klTuAVfkTnOPm6RvagtIke0130 provenance
has publication info: NP54432.RAUNXxIcVbpIf YlDULFN1klTuAVfkTnOPm6RvagtIke0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54432.RAUNXxIcVbpIf YlDULFN1klTuAVfkTnOPm6RvagtIke0130 assertion
type: Assertion
description: [Finally, we claim that determination of MMP-9 enzyme levels and expression of MMP-2 and -9 and TIMP-1 can be used as a marker in lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19814619
was generated by: ECO_0000203

NP54435.RAbE 1ixRo12wkJ3SvyuBLY6fQFs1Amd9vBLp9fbYen20
has assertion: NP54435.RAbE 1ixRo12wkJ3SvyuBLY6fQFs1Amd9vBLp9fbYen20130 assertion
has provenance: NP54435.RAbE 1ixRo12wkJ3SvyuBLY6fQFs1Amd9vBLp9fbYen20130 provenance
has publication info: NP54435.RAbE 1ixRo12wkJ3SvyuBLY6fQFs1Amd9vBLp9fbYen20130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54435.RAbE 1ixRo12wkJ3SvyuBLY6fQFs1Amd9vBLp9fbYen20130 assertion
type: Assertion
description: [We conclude that there are cell host-dependent differences in MMP-9 promoter activity related to CA-repeat number and that fetal carriage of the 14 CA-repeat allele is associated with PPROM in African Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11994547
was generated by: ECO_0000203

NP54436.RAbaPr91d0HNb80zxYd1OwdZ21ZhsPoM3EFzspnnQYZ9s
has assertion: NP54436.RAbaPr91d0HNb80zxYd1OwdZ21ZhsPoM3EFzspnnQYZ9s130 assertion
has provenance: NP54436.RAbaPr91d0HNb80zxYd1OwdZ21ZhsPoM3EFzspnnQYZ9s130 provenance
has publication info: NP54436.RAbaPr91d0HNb80zxYd1OwdZ21ZhsPoM3EFzspnnQYZ9s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54436.RAbaPr91d0HNb80zxYd1OwdZ21ZhsPoM3EFzspnnQYZ9s130 assertion
type: Assertion
description: [Thus, the microsatellite polymorphism upstream of the MMP-9 gene could be a useful genetic marker for diabetic nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11576356
was generated by: ECO_0000203

NP54437.RAbFLhtue8EqRzvGit8xjM ogo68Hmm7lXQAoiFBRMCL0
has assertion: NP54437.RAbFLhtue8EqRzvGit8xjM ogo68Hmm7lXQAoiFBRMCL0130 assertion
has provenance: NP54437.RAbFLhtue8EqRzvGit8xjM ogo68Hmm7lXQAoiFBRMCL0130 provenance
has publication info: NP54437.RAbFLhtue8EqRzvGit8xjM ogo68Hmm7lXQAoiFBRMCL0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54437.RAbFLhtue8EqRzvGit8xjM ogo68Hmm7lXQAoiFBRMCL0130 assertion
type: Assertion
description: [These results suggest that the polymorphism of MMP-9 acts as a genetic factor for the development of smoking-induced pulmonary emphysema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11708786
was generated by: ECO_0000203

NP54439.RAYHhU a3vsBIq8ZMsHwLSxMO-h916 8kv4FZDus9R9 s
has assertion: NP54439.RAYHhU a3vsBIq8ZMsHwLSxMO-h916 8kv4FZDus9R9 s130 assertion
has provenance: NP54439.RAYHhU a3vsBIq8ZMsHwLSxMO-h916 8kv4FZDus9R9 s130 provenance
has publication info: NP54439.RAYHhU a3vsBIq8ZMsHwLSxMO-h916 8kv4FZDus9R9 s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54439.RAYHhU a3vsBIq8ZMsHwLSxMO-h916 8kv4FZDus9R9 s130 assertion
type: Assertion
description: [The use of DNA pooling technology increased the throughput and decreased the cost of our association analysis of nephropathy in our type 2 diabetes sample, which demonstrated sufficient sensitivity to support previous positive findings of association with a microsatellite in the MMP9 promoter region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18587729
was generated by: ECO_0000203

NP54442.RAWRSOwVjg5qZQ76WQBnuyg3yDfVQetxOWwjTmBJdGwaQ
has assertion: NP54442.RAWRSOwVjg5qZQ76WQBnuyg3yDfVQetxOWwjTmBJdGwaQ130 assertion
has provenance: NP54442.RAWRSOwVjg5qZQ76WQBnuyg3yDfVQetxOWwjTmBJdGwaQ130 provenance
has publication info: NP54442.RAWRSOwVjg5qZQ76WQBnuyg3yDfVQetxOWwjTmBJdGwaQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54442.RAWRSOwVjg5qZQ76WQBnuyg3yDfVQetxOWwjTmBJdGwaQ130 assertion
type: Assertion
description: [Accumulation of gene polymorphisms related to plaque rupture and thrombus formation is likely associated with the prevalence of cerebral infarction in type 2 diabetic patients, suggesting that the combined information about these variants is useful to ass]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19933990
was generated by: ECO_0000203

NP54443.RAVM5MwvNzjc26IATAOCW7CLuTqRqXSUpqhEgL4305hs4
has assertion: NP54443.RAVM5MwvNzjc26IATAOCW7CLuTqRqXSUpqhEgL4305hs4130 assertion
has provenance: NP54443.RAVM5MwvNzjc26IATAOCW7CLuTqRqXSUpqhEgL4305hs4130 provenance
has publication info: NP54443.RAVM5MwvNzjc26IATAOCW7CLuTqRqXSUpqhEgL4305hs4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54443.RAVM5MwvNzjc26IATAOCW7CLuTqRqXSUpqhEgL4305hs4130 assertion
type: Assertion
description: [Regulatory polymorphisms in extracellular matrix protease genes and susceptibility to rheumatoid arthritis: a case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16356191
was generated by: ECO_0000203

NP54446.RAXkeHvjJEPbP7lJxG9JrURYhOVxv078EVGsd42dQapJY
has assertion: NP54446.RAXkeHvjJEPbP7lJxG9JrURYhOVxv078EVGsd42dQapJY130 assertion
has provenance: NP54446.RAXkeHvjJEPbP7lJxG9JrURYhOVxv078EVGsd42dQapJY130 provenance
has publication info: NP54446.RAXkeHvjJEPbP7lJxG9JrURYhOVxv078EVGsd42dQapJY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54446.RAXkeHvjJEPbP7lJxG9JrURYhOVxv078EVGsd42dQapJY130 assertion
type: Assertion
description: [These results imply that susceptibility to OSF could involve multigenic mechanisms modified by the betel quid-exposure dose]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12101112
was generated by: ECO_0000203

NP54447.RAUB7JNnNmG8sDaL hDWjVlgcroxmdFnquSm782tiyjEg
has assertion: NP54447.RAUB7JNnNmG8sDaL hDWjVlgcroxmdFnquSm782tiyjEg130 assertion
has provenance: NP54447.RAUB7JNnNmG8sDaL hDWjVlgcroxmdFnquSm782tiyjEg130 provenance
has publication info: NP54447.RAUB7JNnNmG8sDaL hDWjVlgcroxmdFnquSm782tiyjEg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54447.RAUB7JNnNmG8sDaL hDWjVlgcroxmdFnquSm782tiyjEg130 assertion
type: Assertion
description: [ The study suggested that a possible association between the MMP-7 A/G polymorphism with susceptibility to epithelium ovarian cancer, but there is no support for an association of the selected MMP-1 1G/2G, MMP-3 5A/6A, and MMP-9 C/T polymorphisms with the risk for ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16278009
was generated by: ECO_0000203

NP54450.RAfGNyWNCbb7vM6OLSNwExjuo xxtvVrzLkgGtB dAzvM
has assertion: NP54450.RAfGNyWNCbb7vM6OLSNwExjuo xxtvVrzLkgGtB dAzvM130 assertion
has provenance: NP54450.RAfGNyWNCbb7vM6OLSNwExjuo xxtvVrzLkgGtB dAzvM130 provenance
has publication info: NP54450.RAfGNyWNCbb7vM6OLSNwExjuo xxtvVrzLkgGtB dAzvM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54450.RAfGNyWNCbb7vM6OLSNwExjuo xxtvVrzLkgGtB dAzvM130 assertion
type: Assertion
description: [ These findings suggest that genetic variations in TIMP1, TIMP3, MMP10, and ELN genes may contribute to the pathogenesis of AAAs. Further work is needed to confirm the findings in an independent set of samples and to study the functional role of these variants in AAA. It is noteworthy that contrary to a previous study, we did not find an association between the MMP9 (nt-1562) polymorphism and AAA, suggesting genetic heterogeneity of the disease. CLINICAL RELEVANCE: Abdominal aortic aneurysms (AAAs) are an important cardiovascular disease, but the genetic and environmental risk factors, which contribute to individual's risk to develop an aneurysm, are poorly understood. Histologically, AAAs are characterized by signs of chronic inflammation, destructive remodeling of the extracellular matrix, and depletion of vascular smooth muscle cells. We hypothesized that genes involved in these events could harbor changes that make individuals more susceptible to developing aneurysms. This study identified significant genetic associations between DNA sequence changes in tissue inhibitor of metalloproteinase 1 (TIMP1), TIMP3, matrix metalloproteinase 10 (MMP10) and elastin (ELN) genes, and AAA. The results will require confirmation using an independent set of samples. After replication it is possible that these sequence changes in combination with other risk factors could be used in the future to identify individuals who are at increased risk for developing an AAA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15944607
was generated by: ECO_0000203

NP54453.RAdTNml3JfjzjZ390fXSnAMwqySO XWEhAZ3BysjN7G6g
has assertion: NP54453.RAdTNml3JfjzjZ390fXSnAMwqySO XWEhAZ3BysjN7G6g130 assertion
has provenance: NP54453.RAdTNml3JfjzjZ390fXSnAMwqySO XWEhAZ3BysjN7G6g130 provenance
has publication info: NP54453.RAdTNml3JfjzjZ390fXSnAMwqySO XWEhAZ3BysjN7G6g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54453.RAdTNml3JfjzjZ390fXSnAMwqySO XWEhAZ3BysjN7G6g130 assertion
type: Assertion
description: [ The MMP-3 5A allele is associated with the occurrence of CA. Our results suggest that an increased proteolysis in the arterial wall may act as a susceptibility factor for the development of CA in patients with coronary atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12103254
was generated by: ECO_0000203

NP54454.RAf6oZ2Z-W5FsbtqtrgslCqJtk6-h9euBOiDesx5vYHcE
has assertion: NP54454.RAf6oZ2Z-W5FsbtqtrgslCqJtk6-h9euBOiDesx5vYHcE130 assertion
has provenance: NP54454.RAf6oZ2Z-W5FsbtqtrgslCqJtk6-h9euBOiDesx5vYHcE130 provenance
has publication info: NP54454.RAf6oZ2Z-W5FsbtqtrgslCqJtk6-h9euBOiDesx5vYHcE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54454.RAf6oZ2Z-W5FsbtqtrgslCqJtk6-h9euBOiDesx5vYHcE130 assertion
type: Assertion
description: [Multivariate logistic regression analysis, with adjustment for age, body mass index, and the prevalence of smoking and hyperuricemia, revealed that the -219G-->T polymorphism of the apolipoprotein E gene in low-risk men, the -1171/5A-->6A polymorphism of the stromelysin-1 gene in low-risk women, the 1019C-->T polymorphism of the connexin 37 gene in high-risk men, and the 3932T-->C polymorphism of the apolipoprotein E gene in high-risk women were significantly associated with CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14563588
was generated by: ECO_0000203

NP54458.RAejQOpMKXASb47ercqm11AMGcOvJoteA9ab3l1vuSlL0
has assertion: NP54458.RAejQOpMKXASb47ercqm11AMGcOvJoteA9ab3l1vuSlL0130 assertion
has provenance: NP54458.RAejQOpMKXASb47ercqm11AMGcOvJoteA9ab3l1vuSlL0130 provenance
has publication info: NP54458.RAejQOpMKXASb47ercqm11AMGcOvJoteA9ab3l1vuSlL0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54458.RAejQOpMKXASb47ercqm11AMGcOvJoteA9ab3l1vuSlL0130 assertion
type: Assertion
description: [Stromelysin 1 (matrix metalloproteinase 3) and HLA-DRB1 gene polymorphisms: Association with severity and progression of rheumatoid arthritis in a prospective study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12124858
was generated by: ECO_0000203

NP54463.RAXH-pW0EO0XzMz9qtOH51gwHOX8xmMF6q1N4B2tnddH4
has assertion: NP54463.RAXH-pW0EO0XzMz9qtOH51gwHOX8xmMF6q1N4B2tnddH4130 assertion
has provenance: NP54463.RAXH-pW0EO0XzMz9qtOH51gwHOX8xmMF6q1N4B2tnddH4130 provenance
has publication info: NP54463.RAXH-pW0EO0XzMz9qtOH51gwHOX8xmMF6q1N4B2tnddH4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54463.RAXH-pW0EO0XzMz9qtOH51gwHOX8xmMF6q1N4B2tnddH4130 assertion
type: Assertion
description: [The present result suggested that the MMP3 promoter polymorphism may modify susceptibility to NSCLC, and the MMP 1G/5A haplotype may predicate the risk of lymphatic metastasis of this tumor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15528217
was generated by: ECO_0000203

NP54466.RAT1F0l4QradIZfv-ZP RXGFHwlIQArpzHFa1fN362-GA
has assertion: NP54466.RAT1F0l4QradIZfv-ZP RXGFHwlIQArpzHFa1fN362-GA130 assertion
has provenance: NP54466.RAT1F0l4QradIZfv-ZP RXGFHwlIQArpzHFa1fN362-GA130 provenance
has publication info: NP54466.RAT1F0l4QradIZfv-ZP RXGFHwlIQArpzHFa1fN362-GA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54466.RAT1F0l4QradIZfv-ZP RXGFHwlIQArpzHFa1fN362-GA130 assertion
type: Assertion
description: [this study identified SNPs in MMP1, MMP2, MMP7 and MMP12 for further investigation as possible predictors of chemotherapy outcome in lung cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19643940
was generated by: ECO_0000203

NP54471.RAetPF6rmRiCYXgidp4pyNZbidRvlWybkjgQklMVqC02g
has assertion: NP54471.RAetPF6rmRiCYXgidp4pyNZbidRvlWybkjgQklMVqC02g130 assertion
has provenance: NP54471.RAetPF6rmRiCYXgidp4pyNZbidRvlWybkjgQklMVqC02g130 provenance
has publication info: NP54471.RAetPF6rmRiCYXgidp4pyNZbidRvlWybkjgQklMVqC02g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54471.RAetPF6rmRiCYXgidp4pyNZbidRvlWybkjgQklMVqC02g130 assertion
type: Assertion
description: [ The study suggested that a possible association between the MMP-7 A/G polymorphism with susceptibility to epithelium ovarian cancer, but there is no support for an association of the selected MMP-1 1G/2G, MMP-3 5A/6A, and MMP-9 C/T polymorphisms with the risk for ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16278009
was generated by: ECO_0000203

NP54479.RAbp83B3nD55wLm0QuhGByDqqnKTdGULEiWweC4vJI5T0
has assertion: NP54479.RAbp83B3nD55wLm0QuhGByDqqnKTdGULEiWweC4vJI5T0130 assertion
has provenance: NP54479.RAbp83B3nD55wLm0QuhGByDqqnKTdGULEiWweC4vJI5T0130 provenance
has publication info: NP54479.RAbp83B3nD55wLm0QuhGByDqqnKTdGULEiWweC4vJI5T0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54479.RAbp83B3nD55wLm0QuhGByDqqnKTdGULEiWweC4vJI5T0130 assertion
type: Assertion
description: [These data suggest that the MMP-1 promoter polymorphism may be associated with HNSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15194213
was generated by: ECO_0000203

NP54485.RAWwWZrzifcmL4o9UYFoXJg1p86 kbT4d n-gQSNXNL-g
has assertion: NP54485.RAWwWZrzifcmL4o9UYFoXJg1p86 kbT4d n-gQSNXNL-g130 assertion
has provenance: NP54485.RAWwWZrzifcmL4o9UYFoXJg1p86 kbT4d n-gQSNXNL-g130 provenance
has publication info: NP54485.RAWwWZrzifcmL4o9UYFoXJg1p86 kbT4d n-gQSNXNL-g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54485.RAWwWZrzifcmL4o9UYFoXJg1p86 kbT4d n-gQSNXNL-g130 assertion
type: Assertion
description: [A multigenic approach to predict breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17058024
was generated by: ECO_0000203

NP54488.RAbxgXXhGadm1ePdjfHCepu5ULt-OAyWE6pKqxLaeULS8
has assertion: NP54488.RAbxgXXhGadm1ePdjfHCepu5ULt-OAyWE6pKqxLaeULS8130 assertion
has provenance: NP54488.RAbxgXXhGadm1ePdjfHCepu5ULt-OAyWE6pKqxLaeULS8130 provenance
has publication info: NP54488.RAbxgXXhGadm1ePdjfHCepu5ULt-OAyWE6pKqxLaeULS8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54488.RAbxgXXhGadm1ePdjfHCepu5ULt-OAyWE6pKqxLaeULS8130 assertion
type: Assertion
description: [This study provides the first evidence of an association between a polymorphism in the MMP-3 gene promoter and the severity and progression of RA, but not RA susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12124858
was generated by: ECO_0000203

NP54494.RAWeh1ZGcBS8R5K-EN56oyRxQqLQfzRUuWUlGKTmDIJgM
has assertion: NP54494.RAWeh1ZGcBS8R5K-EN56oyRxQqLQfzRUuWUlGKTmDIJgM130 assertion
has provenance: NP54494.RAWeh1ZGcBS8R5K-EN56oyRxQqLQfzRUuWUlGKTmDIJgM130 provenance
has publication info: NP54494.RAWeh1ZGcBS8R5K-EN56oyRxQqLQfzRUuWUlGKTmDIJgM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54494.RAWeh1ZGcBS8R5K-EN56oyRxQqLQfzRUuWUlGKTmDIJgM130 assertion
type: Assertion
description: [Synergistic effect of stromelysin-1 (matrix metallo-proteinase-3) promoter 5A/6A polymorphism with smoking on the onset of young acute myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12876636
was generated by: ECO_0000203

NP54498.RAWhJ1fLtCWd6t8LHv9HDp yHzwM4hO7rr2BOX x7TF4
has assertion: NP54498.RAWhJ1fLtCWd6t8LHv9HDp yHzwM4hO7rr2BOX x7TF4130 assertion
has provenance: NP54498.RAWhJ1fLtCWd6t8LHv9HDp yHzwM4hO7rr2BOX x7TF4130 provenance
has publication info: NP54498.RAWhJ1fLtCWd6t8LHv9HDp yHzwM4hO7rr2BOX x7TF4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54498.RAWhJ1fLtCWd6t8LHv9HDp yHzwM4hO7rr2BOX x7TF4130 assertion
type: Assertion
description: [The aim of our study was to analyze the possible association of eNOS G894 T and MMP-3 5A/6A gene polymorphisms with hypertension in Serbian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16302209
was generated by: ECO_0000203

NP54502.RATXbosU5BVxUZpQ-A83bOgxlH1AYXELEmmKdj98X3bT8
has assertion: NP54502.RATXbosU5BVxUZpQ-A83bOgxlH1AYXELEmmKdj98X3bT8130 assertion
has provenance: NP54502.RATXbosU5BVxUZpQ-A83bOgxlH1AYXELEmmKdj98X3bT8130 provenance
has publication info: NP54502.RATXbosU5BVxUZpQ-A83bOgxlH1AYXELEmmKdj98X3bT8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54502.RATXbosU5BVxUZpQ-A83bOgxlH1AYXELEmmKdj98X3bT8130 assertion
type: Assertion
description: [ Our data strongly suggest that the 5A/6A polymorphism of the stromelysin-1 gene is not related to angiographic restenosis or the 1-year clinical outcome after interventions in coronary arteries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14984923
was generated by: ECO_0000203

NP54505.RAdfwVVCiYMA97bYbQByYbzFJAJvEYtcLLeQ5q6-Pebcg
has assertion: NP54505.RAdfwVVCiYMA97bYbQByYbzFJAJvEYtcLLeQ5q6-Pebcg130 assertion
has provenance: NP54505.RAdfwVVCiYMA97bYbQByYbzFJAJvEYtcLLeQ5q6-Pebcg130 provenance
has publication info: NP54505.RAdfwVVCiYMA97bYbQByYbzFJAJvEYtcLLeQ5q6-Pebcg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54505.RAdfwVVCiYMA97bYbQByYbzFJAJvEYtcLLeQ5q6-Pebcg130 assertion
type: Assertion
description: [The data indicate a key role for stromelysin in the atherosclerotic process. Men with the stromelysin genotype 5A5A represent 29% of the general population, and their high risk, if smokers, provides a further strong argument for smoking avoidance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12485468
was generated by: ECO_0000203

NP54507.RAWqfABKi7IvszUpZ5ywb7N0zB mJSSMfMuHMY9DO6FL0
has assertion: NP54507.RAWqfABKi7IvszUpZ5ywb7N0zB mJSSMfMuHMY9DO6FL0130 assertion
has provenance: NP54507.RAWqfABKi7IvszUpZ5ywb7N0zB mJSSMfMuHMY9DO6FL0130 provenance
has publication info: NP54507.RAWqfABKi7IvszUpZ5ywb7N0zB mJSSMfMuHMY9DO6FL0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54507.RAWqfABKi7IvszUpZ5ywb7N0zB mJSSMfMuHMY9DO6FL0130 assertion
type: Assertion
description: [The roles of stromelysin-1 and the gelatinase B gene polymorphism in stable angina.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12205736
was generated by: ECO_0000203

NP54508.RAXH2cS8kIgqukIVO4aHvAJARF5p uSUwIl0XiG5PD1Zw
has assertion: NP54508.RAXH2cS8kIgqukIVO4aHvAJARF5p uSUwIl0XiG5PD1Zw130 assertion
has provenance: NP54508.RAXH2cS8kIgqukIVO4aHvAJARF5p uSUwIl0XiG5PD1Zw130 provenance
has publication info: NP54508.RAXH2cS8kIgqukIVO4aHvAJARF5p uSUwIl0XiG5PD1Zw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54508.RAXH2cS8kIgqukIVO4aHvAJARF5p uSUwIl0XiG5PD1Zw130 assertion
type: Assertion
description: [We have investigated the influence of a biallelic polymorphism of the promoter region of stromelysin (matrix metalloproteinase 3) on susceptibility to primary sclerosing cholangitis (PSC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11438501
was generated by: ECO_0000203

NP54509.RAdjFXL1ptDgd0IwCDSR7-YEmgSJH 4l9QZHZMUNC1mt0
has assertion: NP54509.RAdjFXL1ptDgd0IwCDSR7-YEmgSJH 4l9QZHZMUNC1mt0130 assertion
has provenance: NP54509.RAdjFXL1ptDgd0IwCDSR7-YEmgSJH 4l9QZHZMUNC1mt0130 provenance
has publication info: NP54509.RAdjFXL1ptDgd0IwCDSR7-YEmgSJH 4l9QZHZMUNC1mt0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54509.RAdjFXL1ptDgd0IwCDSR7-YEmgSJH 4l9QZHZMUNC1mt0130 assertion
type: Assertion
description: [These data imply the involvement of MMP3 in chronic remodelling after conventional balloon angioplasty, and suggest that the 6A6A MMP3 genotype is a genetic susceptibility factor for restenosis after angioplasty without stenting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11977998
was generated by: ECO_0000203

NP54513.RAVG8m4Cv0eNvb0Grcxz6HN98KTw6yU08teYjCwFosuzY
has assertion: NP54513.RAVG8m4Cv0eNvb0Grcxz6HN98KTw6yU08teYjCwFosuzY130 assertion
has provenance: NP54513.RAVG8m4Cv0eNvb0Grcxz6HN98KTw6yU08teYjCwFosuzY130 provenance
has publication info: NP54513.RAVG8m4Cv0eNvb0Grcxz6HN98KTw6yU08teYjCwFosuzY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54513.RAVG8m4Cv0eNvb0Grcxz6HN98KTw6yU08teYjCwFosuzY130 assertion
type: Assertion
description: [The aim of the study was to investigate the effect of functional polymorphisms in promoters of matrix metalloproteinase (MMP) 2, MMP-3, MMP-9, MMP-12 and plasminogen activator inhibitor (PAI) 1 genes on the growth rate of small abdominal aortic aneurysms (AAA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16082623
was generated by: ECO_0000203

NP54515.RAb8geeYpyQG2lMfA9zSSaJsdj0VKWPRxrsa1Nx8H4Scc
has assertion: NP54515.RAb8geeYpyQG2lMfA9zSSaJsdj0VKWPRxrsa1Nx8H4Scc130 assertion
has provenance: NP54515.RAb8geeYpyQG2lMfA9zSSaJsdj0VKWPRxrsa1Nx8H4Scc130 provenance
has publication info: NP54515.RAb8geeYpyQG2lMfA9zSSaJsdj0VKWPRxrsa1Nx8H4Scc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54515.RAb8geeYpyQG2lMfA9zSSaJsdj0VKWPRxrsa1Nx8H4Scc130 assertion
type: Assertion
description: [Genetic approaches to the investigation of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11981324
was generated by: ECO_0000203

NP54522.RAQvl8LTRgAzf-aVMCBm8Fgb53ShdMYfOMFpxphmrsH4I
has assertion: NP54522.RAQvl8LTRgAzf-aVMCBm8Fgb53ShdMYfOMFpxphmrsH4I130 assertion
has provenance: NP54522.RAQvl8LTRgAzf-aVMCBm8Fgb53ShdMYfOMFpxphmrsH4I130 provenance
has publication info: NP54522.RAQvl8LTRgAzf-aVMCBm8Fgb53ShdMYfOMFpxphmrsH4I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54522.RAQvl8LTRgAzf-aVMCBm8Fgb53ShdMYfOMFpxphmrsH4I130 assertion
type: Assertion
description: [These results are consistent with our previous findings and further support the hypothesis that gain-of-function of MMP2 resulting from genetic polymorphisms plays an important role in human carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15731163
was generated by: ECO_0000203

NP54529.RAVVXZIaFCMUFZ4ziH5 b82VtGbKeSCHeL7XSIS9Db44U
has assertion: NP54529.RAVVXZIaFCMUFZ4ziH5 b82VtGbKeSCHeL7XSIS9Db44U130 assertion
has provenance: NP54529.RAVVXZIaFCMUFZ4ziH5 b82VtGbKeSCHeL7XSIS9Db44U130 provenance
has publication info: NP54529.RAVVXZIaFCMUFZ4ziH5 b82VtGbKeSCHeL7XSIS9Db44U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54529.RAVVXZIaFCMUFZ4ziH5 b82VtGbKeSCHeL7XSIS9Db44U130 assertion
type: Assertion
description: [We have demonstrated that several SNPs are associated with survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19094228
was generated by: ECO_0000203

NP54537.RAavDCkNwvRJrHJyf5mGsL2dks7LzAgACDNvI1R rDe8w
has assertion: NP54537.RAavDCkNwvRJrHJyf5mGsL2dks7LzAgACDNvI1R rDe8w130 assertion
has provenance: NP54537.RAavDCkNwvRJrHJyf5mGsL2dks7LzAgACDNvI1R rDe8w130 provenance
has publication info: NP54537.RAavDCkNwvRJrHJyf5mGsL2dks7LzAgACDNvI1R rDe8w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54537.RAavDCkNwvRJrHJyf5mGsL2dks7LzAgACDNvI1R rDe8w130 assertion
type: Assertion
description: [We found that the G/G genotype in the MMP-2-1575G/A polymorphism was significantly increased in colorectal cancer patients than in the controls (odds ratio (OR), 1.96; 95% CI, 1.06-3.64).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17546628
was generated by: ECO_0000203

NP54541.RAZ4FHu9HzK4RIXncc T5wpVBmTb -n0tSHSJBNZVX-lo
has assertion: NP54541.RAZ4FHu9HzK4RIXncc T5wpVBmTb -n0tSHSJBNZVX-lo130 assertion
has provenance: NP54541.RAZ4FHu9HzK4RIXncc T5wpVBmTb -n0tSHSJBNZVX-lo130 provenance
has publication info: NP54541.RAZ4FHu9HzK4RIXncc T5wpVBmTb -n0tSHSJBNZVX-lo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54541.RAZ4FHu9HzK4RIXncc T5wpVBmTb -n0tSHSJBNZVX-lo130 assertion
type: Assertion
description: [Our results suggest MMP-2 and TIMP-2 genotypes play a crucial role in gastric cancer invasion, but not with development of gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17236757
was generated by: ECO_0000203

NP54542.RAVfE MkcrjohNO08EYddnZCGLGC4rpWwrpl6h8EhEP2Y
has assertion: NP54542.RAVfE MkcrjohNO08EYddnZCGLGC4rpWwrpl6h8EhEP2Y130 assertion
has provenance: NP54542.RAVfE MkcrjohNO08EYddnZCGLGC4rpWwrpl6h8EhEP2Y130 provenance
has publication info: NP54542.RAVfE MkcrjohNO08EYddnZCGLGC4rpWwrpl6h8EhEP2Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54542.RAVfE MkcrjohNO08EYddnZCGLGC4rpWwrpl6h8EhEP2Y130 assertion
type: Assertion
description: [This case control study was to assess the contribution of this MMP2 polymorphism to risk of development and metastasis of gastric cardia adenocarcinoma (GCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12873995
was generated by: ECO_0000203

NP54543.RAZE2B77pYulBBQ5WVJSevk6T18XSqvJZrAMwqsKLRTYs
has assertion: NP54543.RAZE2B77pYulBBQ5WVJSevk6T18XSqvJZrAMwqsKLRTYs130 assertion
has provenance: NP54543.RAZE2B77pYulBBQ5WVJSevk6T18XSqvJZrAMwqsKLRTYs130 provenance
has publication info: NP54543.RAZE2B77pYulBBQ5WVJSevk6T18XSqvJZrAMwqsKLRTYs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54543.RAZE2B77pYulBBQ5WVJSevk6T18XSqvJZrAMwqsKLRTYs130 assertion
type: Assertion
description: [Two MMP-2 promoter polymorphisms (-790T/G and -735C/T) in chronic heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14580155
was generated by: ECO_0000203

NP54550.RAfKqk3ef zpyK8RutPyqvqFacQ2D8AztIiUYwDEHe8Xw
has assertion: NP54550.RAfKqk3ef zpyK8RutPyqvqFacQ2D8AztIiUYwDEHe8Xw130 assertion
has provenance: NP54550.RAfKqk3ef zpyK8RutPyqvqFacQ2D8AztIiUYwDEHe8Xw130 provenance
has publication info: NP54550.RAfKqk3ef zpyK8RutPyqvqFacQ2D8AztIiUYwDEHe8Xw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54550.RAfKqk3ef zpyK8RutPyqvqFacQ2D8AztIiUYwDEHe8Xw130 assertion
type: Assertion
description: [A cohort of patients with seropositive rheumatoid arthritis were recruited and genotyped for the MMP1-1607 1G > 2G, MMP3-1612 5A > 6A, MMP7-153C > T, MMP7-181G > A, MMP12-82A > G and MMP13-77A > G polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17373931
was generated by: ECO_0000203

NP54555.RAeW7P1ZYjqrXGU0dHgYtHS7k2bIqhs9quscvDsuy7cVg
has assertion: NP54555.RAeW7P1ZYjqrXGU0dHgYtHS7k2bIqhs9quscvDsuy7cVg130 assertion
has provenance: NP54555.RAeW7P1ZYjqrXGU0dHgYtHS7k2bIqhs9quscvDsuy7cVg130 provenance
has publication info: NP54555.RAeW7P1ZYjqrXGU0dHgYtHS7k2bIqhs9quscvDsuy7cVg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54555.RAeW7P1ZYjqrXGU0dHgYtHS7k2bIqhs9quscvDsuy7cVg130 assertion
type: Assertion
description: [Matrix metalloproteinase single-nucleotide polymorphisms and haplotypes predict breast cancer progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18006768
was generated by: ECO_0000203

NP54556.RAdb1gjVgGolryjnoyZuY1YiUgAWaxBiqv2huqbdVZi0M
has assertion: NP54556.RAdb1gjVgGolryjnoyZuY1YiUgAWaxBiqv2huqbdVZi0M130 assertion
has provenance: NP54556.RAdb1gjVgGolryjnoyZuY1YiUgAWaxBiqv2huqbdVZi0M130 provenance
has publication info: NP54556.RAdb1gjVgGolryjnoyZuY1YiUgAWaxBiqv2huqbdVZi0M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54556.RAdb1gjVgGolryjnoyZuY1YiUgAWaxBiqv2huqbdVZi0M130 assertion
type: Assertion
description: [Genotypes and haplotypes of matrix metalloproteinase 1, 3 and 12 genes and the risk of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16311244
was generated by: ECO_0000203

NP54557.RAUKLn2 UOfeA3zN gWcSP8Sz8zA-QMd81v2TpuVmD5wk
has assertion: NP54557.RAUKLn2 UOfeA3zN gWcSP8Sz8zA-QMd81v2TpuVmD5wk130 assertion
has provenance: NP54557.RAUKLn2 UOfeA3zN gWcSP8Sz8zA-QMd81v2TpuVmD5wk130 provenance
has publication info: NP54557.RAUKLn2 UOfeA3zN gWcSP8Sz8zA-QMd81v2TpuVmD5wk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54557.RAUKLn2 UOfeA3zN gWcSP8Sz8zA-QMd81v2TpuVmD5wk130 assertion
type: Assertion
description: [Our results show that patients with stage I NSCLC carrying the variant G allele of the MMP-12 1082A/G polymorphism have worse survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17000679
was generated by: ECO_0000203

NP54558.RAZBGjGU0nzNpcnvPCnI0OQjffxKia4q0w7f-AUZMXy6A
has assertion: NP54558.RAZBGjGU0nzNpcnvPCnI0OQjffxKia4q0w7f-AUZMXy6A130 assertion
has provenance: NP54558.RAZBGjGU0nzNpcnvPCnI0OQjffxKia4q0w7f-AUZMXy6A130 provenance
has publication info: NP54558.RAZBGjGU0nzNpcnvPCnI0OQjffxKia4q0w7f-AUZMXy6A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54558.RAZBGjGU0nzNpcnvPCnI0OQjffxKia4q0w7f-AUZMXy6A130 assertion
type: Assertion
description: [this study identified SNPs in MMP1, MMP2, MMP7 and MMP12 for further investigation as possible predictors of chemotherapy outcome in lung cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19643940
was generated by: ECO_0000203

NP54560.RAcnPnhBm6w2y-zv5UagiPC74tnKpjd7sa1epXZJergS4
has assertion: NP54560.RAcnPnhBm6w2y-zv5UagiPC74tnKpjd7sa1epXZJergS4130 assertion
has provenance: NP54560.RAcnPnhBm6w2y-zv5UagiPC74tnKpjd7sa1epXZJergS4130 provenance
has publication info: NP54560.RAcnPnhBm6w2y-zv5UagiPC74tnKpjd7sa1epXZJergS4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54560.RAcnPnhBm6w2y-zv5UagiPC74tnKpjd7sa1epXZJergS4130 assertion
type: Assertion
description: [Our findings suggest that there are haplotypes in a MMP cluster region that modify the joint destruction in RA in a phasic manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15142265
was generated by: ECO_0000203

NP54566.RAcpJ3fuBvDetr7Y LO NtW9CJL32bd0Qqay6Mz85XfyM
has assertion: NP54566.RAcpJ3fuBvDetr7Y LO NtW9CJL32bd0Qqay6Mz85XfyM130 assertion
has provenance: NP54566.RAcpJ3fuBvDetr7Y LO NtW9CJL32bd0Qqay6Mz85XfyM130 provenance
has publication info: NP54566.RAcpJ3fuBvDetr7Y LO NtW9CJL32bd0Qqay6Mz85XfyM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54566.RAcpJ3fuBvDetr7Y LO NtW9CJL32bd0Qqay6Mz85XfyM130 assertion
type: Assertion
description: [By using the methods of polymerase chain reaction-restriction fragment length polymorphism analysis (PCR-RFLP), MMP1 -1607(1G>2G) polymorphisms in 150 patients with lung cancer, and 200 healthy controls were detected to evaluate the relationship between different genotypes and susceptibility of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16767672
was generated by: ECO_0000203

NP54567.RAXJEOvmLw5z0tThX8U4UJQjoyQVLV4vpVnh bPcSICmg
has assertion: NP54567.RAXJEOvmLw5z0tThX8U4UJQjoyQVLV4vpVnh bPcSICmg130 assertion
has provenance: NP54567.RAXJEOvmLw5z0tThX8U4UJQjoyQVLV4vpVnh bPcSICmg130 provenance
has publication info: NP54567.RAXJEOvmLw5z0tThX8U4UJQjoyQVLV4vpVnh bPcSICmg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54567.RAXJEOvmLw5z0tThX8U4UJQjoyQVLV4vpVnh bPcSICmg130 assertion
type: Assertion
description: [this study identified SNPs in MMP1, MMP2, MMP7 and MMP12 for further investigation as possible predictors of chemotherapy outcome in lung cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19643940
was generated by: ECO_0000203

NP54569.RAa71KxXgScek6nUhIp8Y75okjS0 lxEd-Nake0gnhqyQ
has assertion: NP54569.RAa71KxXgScek6nUhIp8Y75okjS0 lxEd-Nake0gnhqyQ130 assertion
has provenance: NP54569.RAa71KxXgScek6nUhIp8Y75okjS0 lxEd-Nake0gnhqyQ130 provenance
has publication info: NP54569.RAa71KxXgScek6nUhIp8Y75okjS0 lxEd-Nake0gnhqyQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54569.RAa71KxXgScek6nUhIp8Y75okjS0 lxEd-Nake0gnhqyQ130 assertion
type: Assertion
description: [This study suggests that the polymorphism in MMP8 is associated with a decreased lung cancer risk, which can be used as a prognostic marker in lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19094243
was generated by: ECO_0000203

NP54573.RAeYeLOPBwA huxc9bU-IMcvvTC 1sWKFFXrwg4D8IvnM
has assertion: NP54573.RAeYeLOPBwA huxc9bU-IMcvvTC 1sWKFFXrwg4D8IvnM130 assertion
has provenance: NP54573.RAeYeLOPBwA huxc9bU-IMcvvTC 1sWKFFXrwg4D8IvnM130 provenance
has publication info: NP54573.RAeYeLOPBwA huxc9bU-IMcvvTC 1sWKFFXrwg4D8IvnM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54573.RAeYeLOPBwA huxc9bU-IMcvvTC 1sWKFFXrwg4D8IvnM130 assertion
type: Assertion
description: [Genotypes and haplotypes of matrix metalloproteinase 1, 3 and 12 genes and the risk of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16311244
was generated by: ECO_0000203

NP54578.RAbLBlzeZlpN38Vdmb7sSothkCKthPHa3sKkreOtAuabI
has assertion: NP54578.RAbLBlzeZlpN38Vdmb7sSothkCKthPHa3sKkreOtAuabI130 assertion
has provenance: NP54578.RAbLBlzeZlpN38Vdmb7sSothkCKthPHa3sKkreOtAuabI130 provenance
has publication info: NP54578.RAbLBlzeZlpN38Vdmb7sSothkCKthPHa3sKkreOtAuabI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54578.RAbLBlzeZlpN38Vdmb7sSothkCKthPHa3sKkreOtAuabI130 assertion
type: Assertion
description: [This study aimed to evaluate the association between the MMP-1 promoter gene polymorphism and chronic periodontitis susceptibility and/or severity in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16774538
was generated by: ECO_0000203

NP54581.RAaEo8PUwR0puH -dQgZLev2BlS6fBlxH5eAuI5MqYejM
has assertion: NP54581.RAaEo8PUwR0puH -dQgZLev2BlS6fBlxH5eAuI5MqYejM130 assertion
has provenance: NP54581.RAaEo8PUwR0puH -dQgZLev2BlS6fBlxH5eAuI5MqYejM130 provenance
has publication info: NP54581.RAaEo8PUwR0puH -dQgZLev2BlS6fBlxH5eAuI5MqYejM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54581.RAaEo8PUwR0puH -dQgZLev2BlS6fBlxH5eAuI5MqYejM130 assertion
type: Assertion
description: [The relation between matrix metalloproteinase-1 promoter genotype and remodeling was studied in 42 patients after their first acute myocardial infarctions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15476622
was generated by: ECO_0000203

NP54589.RAedX0FJ3kjs5t--ftEZA9ZcivT6rYMiFyAqCPUasOUw0
has assertion: NP54589.RAedX0FJ3kjs5t--ftEZA9ZcivT6rYMiFyAqCPUasOUw0130 assertion
has provenance: NP54589.RAedX0FJ3kjs5t--ftEZA9ZcivT6rYMiFyAqCPUasOUw0130 provenance
has publication info: NP54589.RAedX0FJ3kjs5t--ftEZA9ZcivT6rYMiFyAqCPUasOUw0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54589.RAedX0FJ3kjs5t--ftEZA9ZcivT6rYMiFyAqCPUasOUw0130 assertion
type: Assertion
description: [These data suggest that the MMP-1 promoter polymorphism may be associated with HNSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15194213
was generated by: ECO_0000203

NP54592.RAVUg3QGjjG4wFFUEsiIAVLqtgTBMEIQOduxDb2lTUCKk
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has publication info: NP54592.RAVUg3QGjjG4wFFUEsiIAVLqtgTBMEIQOduxDb2lTUCKk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
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version: v2.1.0.0

NP54592.RAVUg3QGjjG4wFFUEsiIAVLqtgTBMEIQOduxDb2lTUCKk130 assertion
type: Assertion
description: [The purpose of this study was to investigate the possible relation of matrix metalloproteinase-1 (MMP-1) to increased risk for oral cancer, in light of recently found contribution of angiogenesis and thrombosis-related factors to the development of malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17352267
was generated by: ECO_0000203

NP54602.RAaYZRUg-LFXp7-V1eRpC9g kkZHQaAaM2mAWPzM-YL8I
has assertion: NP54602.RAaYZRUg-LFXp7-V1eRpC9g kkZHQaAaM2mAWPzM-YL8I130 assertion
has provenance: NP54602.RAaYZRUg-LFXp7-V1eRpC9g kkZHQaAaM2mAWPzM-YL8I130 provenance
has publication info: NP54602.RAaYZRUg-LFXp7-V1eRpC9g kkZHQaAaM2mAWPzM-YL8I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54602.RAaYZRUg-LFXp7-V1eRpC9g kkZHQaAaM2mAWPzM-YL8I130 assertion
type: Assertion
description: [The influence of interstitial collagenase-1 genotype polymorphism on colorectal cancer risk in Iranian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18798060
was generated by: ECO_0000203

NP54605.RAbtLbGOEkmqI 4Ow7uPw6jbX4uKLpiUKL25mPROVkDBM
has assertion: NP54605.RAbtLbGOEkmqI 4Ow7uPw6jbX4uKLpiUKL25mPROVkDBM130 assertion
has provenance: NP54605.RAbtLbGOEkmqI 4Ow7uPw6jbX4uKLpiUKL25mPROVkDBM130 provenance
has publication info: NP54605.RAbtLbGOEkmqI 4Ow7uPw6jbX4uKLpiUKL25mPROVkDBM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
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authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54605.RAbtLbGOEkmqI 4Ow7uPw6jbX4uKLpiUKL25mPROVkDBM130 assertion
type: Assertion
description: [ The genetic polymorphisms of MMP-1 are not associated with the risk of HSIL and SCC, but with the invasiveness and prognosis of SCC. The heterozygous genotype of MMP-1 can be used as a prognostic marker in patients with invasive cervical cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15661214
was generated by: ECO_0000203

NP54613.RATbfIbeLbK-mQsve8Lpwd9bPgvTxwpoI4cyn2tQAYtzs
has assertion: NP54613.RATbfIbeLbK-mQsve8Lpwd9bPgvTxwpoI4cyn2tQAYtzs130 assertion
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has publication info: NP54613.RATbfIbeLbK-mQsve8Lpwd9bPgvTxwpoI4cyn2tQAYtzs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54613.RATbfIbeLbK-mQsve8Lpwd9bPgvTxwpoI4cyn2tQAYtzs130 assertion
type: Assertion
description: [Our data suggest that the FAS 1377G>A and IL10 592C>A polymorphisms could modify disease-free and overall survival in women with lymph node-positive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20204402
was generated by: ECO_0000203

NP54614.RAXgzY9aW5PDlLazf 69IF3pBCLNBlxKR7ETS3AIuYu4U
has assertion: NP54614.RAXgzY9aW5PDlLazf 69IF3pBCLNBlxKR7ETS3AIuYu4U130 assertion
has provenance: NP54614.RAXgzY9aW5PDlLazf 69IF3pBCLNBlxKR7ETS3AIuYu4U130 provenance
has publication info: NP54614.RAXgzY9aW5PDlLazf 69IF3pBCLNBlxKR7ETS3AIuYu4U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54614.RAXgzY9aW5PDlLazf 69IF3pBCLNBlxKR7ETS3AIuYu4U130 assertion
type: Assertion
description: [These results suggest that MMP single-nucleotide polymorphisms influence breast cancer behavior and that the MMP-1 2G/2G genotype increases the risk of lymph node metastasis and predicts poor prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18006768
was generated by: ECO_0000203

NP54616.RAdD8LeFVrwETlEp3VBmPKxxxmv5G6r-bYphRPBa4Aw54
has assertion: NP54616.RAdD8LeFVrwETlEp3VBmPKxxxmv5G6r-bYphRPBa4Aw54130 assertion
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has publication info: NP54616.RAdD8LeFVrwETlEp3VBmPKxxxmv5G6r-bYphRPBa4Aw54130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54616.RAdD8LeFVrwETlEp3VBmPKxxxmv5G6r-bYphRPBa4Aw54130 assertion
type: Assertion
description: [A single nucleotide polymorphism in the matrix metalloproteinase-1 promoter is associated with conventional renal cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12845675
was generated by: ECO_0000203

NP54618.RAc5rp8QCu3Peb6Z9QpN5 9SE61PpdSq7k-Q9ueMi1jNc
has assertion: NP54618.RAc5rp8QCu3Peb6Z9QpN5 9SE61PpdSq7k-Q9ueMi1jNc130 assertion
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has publication info: NP54618.RAc5rp8QCu3Peb6Z9QpN5 9SE61PpdSq7k-Q9ueMi1jNc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54618.RAc5rp8QCu3Peb6Z9QpN5 9SE61PpdSq7k-Q9ueMi1jNc130 assertion
type: Assertion
description: [The aims of this study were to investigate (1) the matrix metalloproteinase-1 (MMP-1) promoter polymorphisms in severe chronic periodontitis (CP), (2) the relationship of periodontal therapy outcome with these genotypes, and (3) the gingival crevicular fluid (GCF) MMP-1 levels-MMP-1 genotype correlation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18710412
was generated by: ECO_0000203

NP54628.RARukgSYvR pqCm5xMPmpb4YYI9dBfY gPFLuVZP98t2I
has assertion: NP54628.RARukgSYvR pqCm5xMPmpb4YYI9dBfY gPFLuVZP98t2I130 assertion
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has publication info: NP54628.RARukgSYvR pqCm5xMPmpb4YYI9dBfY gPFLuVZP98t2I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54628.RARukgSYvR pqCm5xMPmpb4YYI9dBfY gPFLuVZP98t2I130 assertion
type: Assertion
description: [Association between neprilysin polymorphisms and sporadic Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17928142
was generated by: ECO_0000203

NP54631.RAVkV52DS0zipjegAT WqaPIzz5bQV8brL8ata2d4sGI4
has assertion: NP54631.RAVkV52DS0zipjegAT WqaPIzz5bQV8brL8ata2d4sGI4130 assertion
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has publication info: NP54631.RAVkV52DS0zipjegAT WqaPIzz5bQV8brL8ata2d4sGI4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54631.RAVkV52DS0zipjegAT WqaPIzz5bQV8brL8ata2d4sGI4130 assertion
type: Assertion
description: [Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16076867
was generated by: ECO_0000203

NP54636.RAVY7PJoo3rG8T5xjt70 wr7353MciauNaCjc223vtYMw
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has publication info: NP54636.RAVY7PJoo3rG8T5xjt70 wr7353MciauNaCjc223vtYMw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54636.RAVY7PJoo3rG8T5xjt70 wr7353MciauNaCjc223vtYMw130 assertion
type: Assertion
description: [The association of IgH rearrangements with ALL-1 alterations in AML, coupled to the frequent detection in this subset of lymphoid associated markers, further supports the origin of these tumors from a common multipotent precursor with bipotential lymphoid and monocytic differentiation capability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/7712464
was generated by: ECO_0000203

NP54643.RAcHKhWFBSa wWXEYHBRviZZbuuc2NsaZDIvfTRcyR0kY
has assertion: NP54643.RAcHKhWFBSa wWXEYHBRviZZbuuc2NsaZDIvfTRcyR0kY130 assertion
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has publication info: NP54643.RAcHKhWFBSa wWXEYHBRviZZbuuc2NsaZDIvfTRcyR0kY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54643.RAcHKhWFBSa wWXEYHBRviZZbuuc2NsaZDIvfTRcyR0kY130 assertion
type: Assertion
description: [PTGS2 and ERCC5 were associated with stomach cancer risk in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19661089
was generated by: ECO_0000203

NP54646.RAUS RWTZZ7rrRC-oTB6Ji aWVq2SRDnIIiU84iyAWJAc
has assertion: NP54646.RAUS RWTZZ7rrRC-oTB6Ji aWVq2SRDnIIiU84iyAWJAc130 assertion
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has publication info: NP54646.RAUS RWTZZ7rrRC-oTB6Ji aWVq2SRDnIIiU84iyAWJAc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54646.RAUS RWTZZ7rrRC-oTB6Ji aWVq2SRDnIIiU84iyAWJAc130 assertion
type: Assertion
description: [Significant differences in allele frequencies between cases and controls were observed for ID3 (inhibitor of DNA binding), p = 0.05, HPN (hepsin), p = 0.009, BCAS1 (breast carcinoma amplified sequence 1), p = 0.007, CAV2 (caveolin 2), p = 0.007, EMP3 (epithelial membrane protein 3), p < 0.0001, and MLH1 (mutL homolog 1), p < 0.0001. SNPs in three of these genes (BCAS1, EMP3 and MLH1) remained significant in an age-matched subsample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15583422
was generated by: ECO_0000203

NP54648.RAVkQA3FdtlXxCiwgEifCvfdSl6R-y9pKiOKdJfllrkdE
has assertion: NP54648.RAVkQA3FdtlXxCiwgEifCvfdSl6R-y9pKiOKdJfllrkdE130 assertion
has provenance: NP54648.RAVkQA3FdtlXxCiwgEifCvfdSl6R-y9pKiOKdJfllrkdE130 provenance
has publication info: NP54648.RAVkQA3FdtlXxCiwgEifCvfdSl6R-y9pKiOKdJfllrkdE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54648.RAVkQA3FdtlXxCiwgEifCvfdSl6R-y9pKiOKdJfllrkdE130 assertion
type: Assertion
description: [Germ-line mutations in mismatch repair genes associated with prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19723918
was generated by: ECO_0000203

NP54660.RAYNDMwdzkSoKfAEQ01CuZxJUzxxw23RTGNo0jFLxkG6I
has assertion: NP54660.RAYNDMwdzkSoKfAEQ01CuZxJUzxxw23RTGNo0jFLxkG6I130 assertion
has provenance: NP54660.RAYNDMwdzkSoKfAEQ01CuZxJUzxxw23RTGNo0jFLxkG6I130 provenance
has publication info: NP54660.RAYNDMwdzkSoKfAEQ01CuZxJUzxxw23RTGNo0jFLxkG6I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54660.RAYNDMwdzkSoKfAEQ01CuZxJUzxxw23RTGNo0jFLxkG6I130 assertion
type: Assertion
description: [Genotype-phenotype correlations in individuals with a founder mutation in the MLH1 gene and hereditary non-polyposis colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17505997
was generated by: ECO_0000203

NP54666.RAT FWr2GWozvTALywrYGpwR0Dwn8Y-ysrvD01VKOLFbI
has assertion: NP54666.RAT FWr2GWozvTALywrYGpwR0Dwn8Y-ysrvD01VKOLFbI130 assertion
has provenance: NP54666.RAT FWr2GWozvTALywrYGpwR0Dwn8Y-ysrvD01VKOLFbI130 provenance
has publication info: NP54666.RAT FWr2GWozvTALywrYGpwR0Dwn8Y-ysrvD01VKOLFbI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54666.RAT FWr2GWozvTALywrYGpwR0Dwn8Y-ysrvD01VKOLFbI130 assertion
type: Assertion
description: [These results suggest that the hMLH1 -93G-->A polymorphism could be used as a marker of genetic susceptibility to squamous cell carcinoma of the lung.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15382050
was generated by: ECO_0000203

NP54670.RAePFhzr-ZqWttySC0uEl0z1CAHK5YcAdIUc6S28dvsjY
has assertion: NP54670.RAePFhzr-ZqWttySC0uEl0z1CAHK5YcAdIUc6S28dvsjY130 assertion
has provenance: NP54670.RAePFhzr-ZqWttySC0uEl0z1CAHK5YcAdIUc6S28dvsjY130 provenance
has publication info: NP54670.RAePFhzr-ZqWttySC0uEl0z1CAHK5YcAdIUc6S28dvsjY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54670.RAePFhzr-ZqWttySC0uEl0z1CAHK5YcAdIUc6S28dvsjY130 assertion
type: Assertion
description: [In this study, we investigated whether singlenucleotide polymorphisms (SNPs) in human mutS homolog 2 (hMSH2) and the human mutL homolog 1 (hMLH1) were associated with the tumor response in advanced NSCLC patients received platinum-based chemotherapy in Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20458443
was generated by: ECO_0000203

NP54671.RAdXwCm1lKdesrF9ZhQEs9 wN4ufq IaEnLYtZEAqZWhU
has assertion: NP54671.RAdXwCm1lKdesrF9ZhQEs9 wN4ufq IaEnLYtZEAqZWhU130 assertion
has provenance: NP54671.RAdXwCm1lKdesrF9ZhQEs9 wN4ufq IaEnLYtZEAqZWhU130 provenance
has publication info: NP54671.RAdXwCm1lKdesrF9ZhQEs9 wN4ufq IaEnLYtZEAqZWhU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54671.RAdXwCm1lKdesrF9ZhQEs9 wN4ufq IaEnLYtZEAqZWhU130 assertion
type: Assertion
description: [Comprehensive analysis of DNA repair gene polymorphisms and survival in patients with early stage non-small-cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20731661
was generated by: ECO_0000203

NP54674.RAYlOpRQz6b-Qa5gIde3074sOOIfKXm-TMJ5Atzom9rTA
has assertion: NP54674.RAYlOpRQz6b-Qa5gIde3074sOOIfKXm-TMJ5Atzom9rTA130 assertion
has provenance: NP54674.RAYlOpRQz6b-Qa5gIde3074sOOIfKXm-TMJ5Atzom9rTA130 provenance
has publication info: NP54674.RAYlOpRQz6b-Qa5gIde3074sOOIfKXm-TMJ5Atzom9rTA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54674.RAYlOpRQz6b-Qa5gIde3074sOOIfKXm-TMJ5Atzom9rTA130 assertion
type: Assertion
description: [Association of Crohn's disease and ulcerative colitis with haplotypes of the MLH1 gene in Italian inflammatory bowel disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12011151
was generated by: ECO_0000203

NP54676.RARw-VGc0Fqd68McSwFBNHFLfEL9tR0qVdM1-VORnQpsA
has assertion: NP54676.RARw-VGc0Fqd68McSwFBNHFLfEL9tR0qVdM1-VORnQpsA130 assertion
has provenance: NP54676.RARw-VGc0Fqd68McSwFBNHFLfEL9tR0qVdM1-VORnQpsA130 provenance
has publication info: NP54676.RARw-VGc0Fqd68McSwFBNHFLfEL9tR0qVdM1-VORnQpsA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54676.RARw-VGc0Fqd68McSwFBNHFLfEL9tR0qVdM1-VORnQpsA130 assertion
type: Assertion
description: [To analyze the genetic contribution of HLA in development of psoriatic arthritis (PsA) and to study whether MICA is primarily associated with PsA or whether its association is secondary to linkage disequilibrium with centromeric genes, such as MICB, TNFA, or HLA-DRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12022360
was generated by: ECO_0000203

NP54678.RAd1Fj2YwJNGMrNtTn97hC9ohXudVkYYcF0pjXf446McU
has assertion: NP54678.RAd1Fj2YwJNGMrNtTn97hC9ohXudVkYYcF0pjXf446McU130 assertion
has provenance: NP54678.RAd1Fj2YwJNGMrNtTn97hC9ohXudVkYYcF0pjXf446McU130 provenance
has publication info: NP54678.RAd1Fj2YwJNGMrNtTn97hC9ohXudVkYYcF0pjXf446McU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54678.RAd1Fj2YwJNGMrNtTn97hC9ohXudVkYYcF0pjXf446McU130 assertion
type: Assertion
description: [The frequency of the MICA-MICB null haplotype was 3.7% on the average, and was strongly associated with HLA-B48 in seven East Asian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11169252
was generated by: ECO_0000203

NP54684.RAY0OAolBy-fn41f Nb6wtB2Ix0SZGdeOYC50n8-q2s20
has assertion: NP54684.RAY0OAolBy-fn41f Nb6wtB2Ix0SZGdeOYC50n8-q2s20130 assertion
has provenance: NP54684.RAY0OAolBy-fn41f Nb6wtB2Ix0SZGdeOYC50n8-q2s20130 provenance
has publication info: NP54684.RAY0OAolBy-fn41f Nb6wtB2Ix0SZGdeOYC50n8-q2s20130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54684.RAY0OAolBy-fn41f Nb6wtB2Ix0SZGdeOYC50n8-q2s20130 assertion
type: Assertion
description: [The allele frequency of MICA*A9 significantly decreased in RA patients compared with controls (9.0% vs. 15.3%, odds ratio OR = 0.55, p = 0.0098, p(c) = 0.049), whereas the frequency of the MICA*A4 and MICA*A5.1 alleles tended to increase in RA patients (21.2% vs. 14.8%, OR = 1.55, p = 0.018, p(c) > 0.05; 20.5% vs. 15.0%, OR = 1.46, p = 0.0403, p(c) > 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14630402
was generated by: ECO_0000203

NP54693.RAfyItKyAYvJY9W7tDqw5Be6R5Jb26NgE2zScwm5Ufvh8
has assertion: NP54693.RAfyItKyAYvJY9W7tDqw5Be6R5Jb26NgE2zScwm5Ufvh8130 assertion
has provenance: NP54693.RAfyItKyAYvJY9W7tDqw5Be6R5Jb26NgE2zScwm5Ufvh8130 provenance
has publication info: NP54693.RAfyItKyAYvJY9W7tDqw5Be6R5Jb26NgE2zScwm5Ufvh8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54693.RAfyItKyAYvJY9W7tDqw5Be6R5Jb26NgE2zScwm5Ufvh8130 assertion
type: Assertion
description: [Increased prevalence of celiac disease without gastrointestinal symptoms in adults MICA 5.1 homozygous subjects from the Campania area.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18282752
was generated by: ECO_0000203

NP54698.RAY9y mNnYJs3Kp1iFSnBTf0eRLbLAKLy8yfCyJ4wba3M
has assertion: NP54698.RAY9y mNnYJs3Kp1iFSnBTf0eRLbLAKLy8yfCyJ4wba3M130 assertion
has provenance: NP54698.RAY9y mNnYJs3Kp1iFSnBTf0eRLbLAKLy8yfCyJ4wba3M130 provenance
has publication info: NP54698.RAY9y mNnYJs3Kp1iFSnBTf0eRLbLAKLy8yfCyJ4wba3M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54698.RAY9y mNnYJs3Kp1iFSnBTf0eRLbLAKLy8yfCyJ4wba3M130 assertion
type: Assertion
description: [ The above-mentioned pattern, most likely formed by recombination of the telomeric fragment of the MHC 7.1 ancestral haplotype, seems to be the most important genetic determinant of susceptibility to the extensive form of UC in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16116311
was generated by: ECO_0000203

NP54704.RAUm32T7lUzW9l91Y1jKFyT1SGwAmw2gN5tLcKFL OBzg
has assertion: NP54704.RAUm32T7lUzW9l91Y1jKFyT1SGwAmw2gN5tLcKFL OBzg130 assertion
has provenance: NP54704.RAUm32T7lUzW9l91Y1jKFyT1SGwAmw2gN5tLcKFL OBzg130 provenance
has publication info: NP54704.RAUm32T7lUzW9l91Y1jKFyT1SGwAmw2gN5tLcKFL OBzg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54704.RAUm32T7lUzW9l91Y1jKFyT1SGwAmw2gN5tLcKFL OBzg130 assertion
type: Assertion
description: [This finding suggests that an association between MICA-A6 and BD may be a secondary phenomenon related to HLA-B51.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16767211
was generated by: ECO_0000203

NP54705.RARgaJbrgmdnQU-m5Z E9r4UylhxPo7ehttVujEDtOqQ
has assertion: NP54705.RARgaJbrgmdnQU-m5Z E9r4UylhxPo7ehttVujEDtOqQ130 assertion
has provenance: NP54705.RARgaJbrgmdnQU-m5Z E9r4UylhxPo7ehttVujEDtOqQ130 provenance
has publication info: NP54705.RARgaJbrgmdnQU-m5Z E9r4UylhxPo7ehttVujEDtOqQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54705.RARgaJbrgmdnQU-m5Z E9r4UylhxPo7ehttVujEDtOqQ130 assertion
type: Assertion
description: [Allelic diversity and affinity variants of MICA are imbalanced in Spanish patients with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16784494
was generated by: ECO_0000203

NP54709.RAQTZTmPwGkMwAP LifSzhEw51 YoK7iL2yQrmQ9hINsE
has assertion: NP54709.RAQTZTmPwGkMwAP LifSzhEw51 YoK7iL2yQrmQ9hINsE130 assertion
has provenance: NP54709.RAQTZTmPwGkMwAP LifSzhEw51 YoK7iL2yQrmQ9hINsE130 provenance
has publication info: NP54709.RAQTZTmPwGkMwAP LifSzhEw51 YoK7iL2yQrmQ9hINsE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54709.RAQTZTmPwGkMwAP LifSzhEw51 YoK7iL2yQrmQ9hINsE130 assertion
type: Assertion
description: [Association of the MIC-A gene and HLA-B51 with Behet's disease in Arabs and non-Ashkenazi Jews in Israel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11796403
was generated by: ECO_0000203

NP54710.RAWAXrdXvlQQ8RSMO4Fu9pgt Gj6-Uf1pLufR1ZI4EXws
has assertion: NP54710.RAWAXrdXvlQQ8RSMO4Fu9pgt Gj6-Uf1pLufR1ZI4EXws130 assertion
has provenance: NP54710.RAWAXrdXvlQQ8RSMO4Fu9pgt Gj6-Uf1pLufR1ZI4EXws130 provenance
has publication info: NP54710.RAWAXrdXvlQQ8RSMO4Fu9pgt Gj6-Uf1pLufR1ZI4EXws130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54710.RAWAXrdXvlQQ8RSMO4Fu9pgt Gj6-Uf1pLufR1ZI4EXws130 assertion
type: Assertion
description: [Triplet repeat polymorphism in the transmembrane region of the MICA gene: a strong association of six GCT repetitions with Behet disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9037047
was generated by: ECO_0000203

NP54712.RAX5F-HZZMNsb5BjfRHVlnTZYEcPYKv7Kqej8YSFaYGkw
has assertion: NP54712.RAX5F-HZZMNsb5BjfRHVlnTZYEcPYKv7Kqej8YSFaYGkw130 assertion
has provenance: NP54712.RAX5F-HZZMNsb5BjfRHVlnTZYEcPYKv7Kqej8YSFaYGkw130 provenance
has publication info: NP54712.RAX5F-HZZMNsb5BjfRHVlnTZYEcPYKv7Kqej8YSFaYGkw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54712.RAX5F-HZZMNsb5BjfRHVlnTZYEcPYKv7Kqej8YSFaYGkw130 assertion
type: Assertion
description: [There are several susceptibility genes for psoriasis residing in chromosome 6p near the HLA-C locus, including the corneodesmosin (CDSN) gene, the octamer transcription factor-3 (POU5F1) gene, the major histocompatibility complex class I chain-related gene A (MICA), and the gene for tumour necrosis factor (TNF)-alpha.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12653732
was generated by: ECO_0000203

NP54714.RASRhEgqhx0QHS3roURz6n63R7 JXFlwKaFiY8Ew-iIqU
has assertion: NP54714.RASRhEgqhx0QHS3roURz6n63R7 JXFlwKaFiY8Ew-iIqU130 assertion
has provenance: NP54714.RASRhEgqhx0QHS3roURz6n63R7 JXFlwKaFiY8Ew-iIqU130 provenance
has publication info: NP54714.RASRhEgqhx0QHS3roURz6n63R7 JXFlwKaFiY8Ew-iIqU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54714.RASRhEgqhx0QHS3roURz6n63R7 JXFlwKaFiY8Ew-iIqU130 assertion
type: Assertion
description: [Our results suggest that the MICA 5.1 allele might be a genetic marker related to the early onset of psoriasis and play a secondary role to the HLA-Cw*0602 gene or an unknown causative gene closely linked to HLA-Cw*0602 in the genetic susceptibility to psoriasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11169245
was generated by: ECO_0000203

NP54715.RARs GGafcHt5PaAdJ-pIafxI2umWPtSw3JO-sASSJuKM
has assertion: NP54715.RARs GGafcHt5PaAdJ-pIafxI2umWPtSw3JO-sASSJuKM130 assertion
has provenance: NP54715.RARs GGafcHt5PaAdJ-pIafxI2umWPtSw3JO-sASSJuKM130 provenance
has publication info: NP54715.RARs GGafcHt5PaAdJ-pIafxI2umWPtSw3JO-sASSJuKM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54715.RARs GGafcHt5PaAdJ-pIafxI2umWPtSw3JO-sASSJuKM130 assertion
type: Assertion
description: [A comparison of the psoriasis patients and the control group revealed that MICA*010 and MICA*017 were associated with Type I psoriasis whereas only MICA*010 was associated with Type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15140030
was generated by: ECO_0000203

NP54718.RATsLzj5chTyZ-OpCq1f8RnYDL90n ZFZIPw6sOyohFKg
has assertion: NP54718.RATsLzj5chTyZ-OpCq1f8RnYDL90n ZFZIPw6sOyohFKg130 assertion
has provenance: NP54718.RATsLzj5chTyZ-OpCq1f8RnYDL90n ZFZIPw6sOyohFKg130 provenance
has publication info: NP54718.RATsLzj5chTyZ-OpCq1f8RnYDL90n ZFZIPw6sOyohFKg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54718.RATsLzj5chTyZ-OpCq1f8RnYDL90n ZFZIPw6sOyohFKg130 assertion
type: Assertion
description: [ MICA gene displayed different allele distributions in different populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12170475
was generated by: ECO_0000203

NP54722.RAa0fjrReqEkOkaEQuMh7tizbg1GexKEHkeWZZ3XaEoWA
has assertion: NP54722.RAa0fjrReqEkOkaEQuMh7tizbg1GexKEHkeWZZ3XaEoWA130 assertion
has provenance: NP54722.RAa0fjrReqEkOkaEQuMh7tizbg1GexKEHkeWZZ3XaEoWA130 provenance
has publication info: NP54722.RAa0fjrReqEkOkaEQuMh7tizbg1GexKEHkeWZZ3XaEoWA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54722.RAa0fjrReqEkOkaEQuMh7tizbg1GexKEHkeWZZ3XaEoWA130 assertion
type: Assertion
description: [ Alleles of MICA gene exon 5 are conservative in all populations studied so far. The results suggest that genetically BMT might be an independent ethnic population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11110982
was generated by: ECO_0000203

NP54723.RAfV8FbDCOX0xtv9ONix8vi8g-wSClTbTrjjdWyEWrJAI
has assertion: NP54723.RAfV8FbDCOX0xtv9ONix8vi8g-wSClTbTrjjdWyEWrJAI130 assertion
has provenance: NP54723.RAfV8FbDCOX0xtv9ONix8vi8g-wSClTbTrjjdWyEWrJAI130 provenance
has publication info: NP54723.RAfV8FbDCOX0xtv9ONix8vi8g-wSClTbTrjjdWyEWrJAI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54723.RAfV8FbDCOX0xtv9ONix8vi8g-wSClTbTrjjdWyEWrJAI130 assertion
type: Assertion
description: [We conclude that the MICA alanine repeat is not a disease-associated factor in POHS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12963865
was generated by: ECO_0000203

NP54726.RAboAYF90Sg13A2KIm6caMf37kFQ9JdvLytQBLGWRvAns
has assertion: NP54726.RAboAYF90Sg13A2KIm6caMf37kFQ9JdvLytQBLGWRvAns130 assertion
has provenance: NP54726.RAboAYF90Sg13A2KIm6caMf37kFQ9JdvLytQBLGWRvAns130 provenance
has publication info: NP54726.RAboAYF90Sg13A2KIm6caMf37kFQ9JdvLytQBLGWRvAns130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54726.RAboAYF90Sg13A2KIm6caMf37kFQ9JdvLytQBLGWRvAns130 assertion
type: Assertion
description: [Evaluation of the microsomal glutathione S-transferase 3 (MGST3) locus on 1q23 as a Type 2 diabetes susceptibility gene in Pima Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12898215
was generated by: ECO_0000203

NP54733.RAWxSgqYW2FurlfOvDnBvfCx0CQ3QSIrTV0pImF20chvQ
has assertion: NP54733.RAWxSgqYW2FurlfOvDnBvfCx0CQ3QSIrTV0pImF20chvQ130 assertion
has provenance: NP54733.RAWxSgqYW2FurlfOvDnBvfCx0CQ3QSIrTV0pImF20chvQ130 provenance
has publication info: NP54733.RAWxSgqYW2FurlfOvDnBvfCx0CQ3QSIrTV0pImF20chvQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54733.RAWxSgqYW2FurlfOvDnBvfCx0CQ3QSIrTV0pImF20chvQ130 assertion
type: Assertion
description: [Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18676680
was generated by: ECO_0000203

NP54735.RAVAIYEv7G5G00iWvoMsj4JR1obujVaf0orglhJwJdw-Y
has assertion: NP54735.RAVAIYEv7G5G00iWvoMsj4JR1obujVaf0orglhJwJdw-Y130 assertion
has provenance: NP54735.RAVAIYEv7G5G00iWvoMsj4JR1obujVaf0orglhJwJdw-Y130 provenance
has publication info: NP54735.RAVAIYEv7G5G00iWvoMsj4JR1obujVaf0orglhJwJdw-Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54735.RAVAIYEv7G5G00iWvoMsj4JR1obujVaf0orglhJwJdw-Y130 assertion
type: Assertion
description: [Comprehensive analysis of DNA repair gene polymorphisms and survival in patients with early stage non-small-cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20731661
was generated by: ECO_0000203

NP54740.RAZwHhrgH31zoi2vNzRKUTo30Degte7fQsS-Mq1D3lCBQ
has assertion: NP54740.RAZwHhrgH31zoi2vNzRKUTo30Degte7fQsS-Mq1D3lCBQ130 assertion
has provenance: NP54740.RAZwHhrgH31zoi2vNzRKUTo30Degte7fQsS-Mq1D3lCBQ130 provenance
has publication info: NP54740.RAZwHhrgH31zoi2vNzRKUTo30Degte7fQsS-Mq1D3lCBQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54740.RAZwHhrgH31zoi2vNzRKUTo30Degte7fQsS-Mq1D3lCBQ130 assertion
type: Assertion
description: [Among whites, carriage of the MGMT Phe84 odds ratio (OR), 0.71; 95% confidence interval (95% CI), 0.51-0.98 or Val143 (OR, 0.66; 95% CI, 0.47-0.92) allele was associated with a decreased risk of head and neck cancer; the haplotype distribution for MGMT differed significantly between cases and controls (covariate-adjusted global permutation test, P = 0.012).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16030112
was generated by: ECO_0000203

NP54741.RAcw-naFCb5EDscm8iwzta3rnxTSJtIQxPstWf8xORTco
has assertion: NP54741.RAcw-naFCb5EDscm8iwzta3rnxTSJtIQxPstWf8xORTco130 assertion
has provenance: NP54741.RAcw-naFCb5EDscm8iwzta3rnxTSJtIQxPstWf8xORTco130 provenance
has publication info: NP54741.RAcw-naFCb5EDscm8iwzta3rnxTSJtIQxPstWf8xORTco130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54741.RAcw-naFCb5EDscm8iwzta3rnxTSJtIQxPstWf8xORTco130 assertion
type: Assertion
description: [ Polymorphisms in the DNA repair enzyme gene XRCC3 241Met was associated with an increased risk of second neoplasms, and polymorphisms of the XRCC1 399Gln gene were associated with a decreased risk of all-cause mortality in patients with primary OSCC. These findings require confirmation in other populations before the clinical implications can be considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16369171
was generated by: ECO_0000203

NP54742.RAYCb 1AfLIIjLR8wJPmebrirT8MmZx97pML32O r9MJo
has assertion: NP54742.RAYCb 1AfLIIjLR8wJPmebrirT8MmZx97pML32O r9MJo130 assertion
has provenance: NP54742.RAYCb 1AfLIIjLR8wJPmebrirT8MmZx97pML32O r9MJo130 provenance
has publication info: NP54742.RAYCb 1AfLIIjLR8wJPmebrirT8MmZx97pML32O r9MJo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54742.RAYCb 1AfLIIjLR8wJPmebrirT8MmZx97pML32O r9MJo130 assertion
type: Assertion
description: [Polymorphism in DNA repair genes and oral squamous cell carcinoma in Thailand.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16373199
was generated by: ECO_0000203

NP54744.RAa9yTSqqvkz ajUdbROpDN9R3VvXBpOLeUuQ6w5EFtyk
has assertion: NP54744.RAa9yTSqqvkz ajUdbROpDN9R3VvXBpOLeUuQ6w5EFtyk130 assertion
has provenance: NP54744.RAa9yTSqqvkz ajUdbROpDN9R3VvXBpOLeUuQ6w5EFtyk130 provenance
has publication info: NP54744.RAa9yTSqqvkz ajUdbROpDN9R3VvXBpOLeUuQ6w5EFtyk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54744.RAa9yTSqqvkz ajUdbROpDN9R3VvXBpOLeUuQ6w5EFtyk130 assertion
type: Assertion
description: [Pooled data from two population-based studies (1,457 cases and 1,351 controls) were analyzed to examine associations between 28 single-nucleotide polymorphisms (SNPs) in nine DNA repair genes (APEX1, BRCA2, ERCC2, ERCC4, MGMT, MUTYH, OGG1, XPC, and XRCC1) and prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19902366
was generated by: ECO_0000203

NP54745.RAbgppE6RHC1AnPGxQTeAfBLogmD9PvvCKfoB7Si75sAA
has assertion: NP54745.RAbgppE6RHC1AnPGxQTeAfBLogmD9PvvCKfoB7Si75sAA130 assertion
has provenance: NP54745.RAbgppE6RHC1AnPGxQTeAfBLogmD9PvvCKfoB7Si75sAA130 provenance
has publication info: NP54745.RAbgppE6RHC1AnPGxQTeAfBLogmD9PvvCKfoB7Si75sAA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54745.RAbgppE6RHC1AnPGxQTeAfBLogmD9PvvCKfoB7Si75sAA130 assertion
type: Assertion
description: [We investigated interactions between dietary factors and the MGMT Ile143Val polymorphism in relation to breast, colorectal and prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20096652
was generated by: ECO_0000203

NP54748.RASaiCPrZLSmea6-I-T3w5cd0BF8hEIuAHi2L9eyBtA98
has assertion: NP54748.RASaiCPrZLSmea6-I-T3w5cd0BF8hEIuAHi2L9eyBtA98130 assertion
has provenance: NP54748.RASaiCPrZLSmea6-I-T3w5cd0BF8hEIuAHi2L9eyBtA98130 provenance
has publication info: NP54748.RASaiCPrZLSmea6-I-T3w5cd0BF8hEIuAHi2L9eyBtA98130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54748.RASaiCPrZLSmea6-I-T3w5cd0BF8hEIuAHi2L9eyBtA98130 assertion
type: Assertion
description: [MGMT genotype modulates the associations between cigarette smoking, dietary antioxidants and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16014702
was generated by: ECO_0000203

NP54751.RAVrTvsdw2WPG90fI2VhtSlJYpxndMZPsA1h2mzcsRwms
has assertion: NP54751.RAVrTvsdw2WPG90fI2VhtSlJYpxndMZPsA1h2mzcsRwms130 assertion
has provenance: NP54751.RAVrTvsdw2WPG90fI2VhtSlJYpxndMZPsA1h2mzcsRwms130 provenance
has publication info: NP54751.RAVrTvsdw2WPG90fI2VhtSlJYpxndMZPsA1h2mzcsRwms130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54751.RAVrTvsdw2WPG90fI2VhtSlJYpxndMZPsA1h2mzcsRwms130 assertion
type: Assertion
description: [In conclusion, these two MGMT polymorphisms may jointly play a role, in the etiology of bladder cancer in southern Chinese population. Larger studies are warranted to validate our findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15885889
was generated by: ECO_0000203

NP54753.RAZVWW9ATiTqBIX10j1g2ejNnpcAZxOAf1MQMrNwf0sC0
has assertion: NP54753.RAZVWW9ATiTqBIX10j1g2ejNnpcAZxOAf1MQMrNwf0sC0130 assertion
has provenance: NP54753.RAZVWW9ATiTqBIX10j1g2ejNnpcAZxOAf1MQMrNwf0sC0130 provenance
has publication info: NP54753.RAZVWW9ATiTqBIX10j1g2ejNnpcAZxOAf1MQMrNwf0sC0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54753.RAZVWW9ATiTqBIX10j1g2ejNnpcAZxOAf1MQMrNwf0sC0130 assertion
type: Assertion
description: [Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19692168
was generated by: ECO_0000203

NP54756.RAZEfMgtRKSa1A qu4eTv0LkzYMJy-HrOb5dVM VV4tgk
has assertion: NP54756.RAZEfMgtRKSa1A qu4eTv0LkzYMJy-HrOb5dVM VV4tgk130 assertion
has provenance: NP54756.RAZEfMgtRKSa1A qu4eTv0LkzYMJy-HrOb5dVM VV4tgk130 provenance
has publication info: NP54756.RAZEfMgtRKSa1A qu4eTv0LkzYMJy-HrOb5dVM VV4tgk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54756.RAZEfMgtRKSa1A qu4eTv0LkzYMJy-HrOb5dVM VV4tgk130 assertion
type: Assertion
description: [In our study, we examined the presence of alterations in MEN1 gene in a series of 39 patients who had undergone surgery for sporadic pHPT (35 with parathyroid adenoma or hyperplasia, 4 with a carcinoma).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15754732
was generated by: ECO_0000203

NP54758.RAdnZSS6QcAVbjdEXH4XGsoYD 6voV2Ug1ryCDqJCkUW4
has assertion: NP54758.RAdnZSS6QcAVbjdEXH4XGsoYD 6voV2Ug1ryCDqJCkUW4130 assertion
has provenance: NP54758.RAdnZSS6QcAVbjdEXH4XGsoYD 6voV2Ug1ryCDqJCkUW4130 provenance
has publication info: NP54758.RAdnZSS6QcAVbjdEXH4XGsoYD 6voV2Ug1ryCDqJCkUW4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54758.RAdnZSS6QcAVbjdEXH4XGsoYD 6voV2Ug1ryCDqJCkUW4130 assertion
type: Assertion
description: [Should routine analysis of the MEN1 gene be performed in all patients with primary hyperparathyroidism under 40 years of age?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20058152
was generated by: ECO_0000203

NP54761.RAVW3ZXZF1DLiXfNov3Ngul82Xvw0xuZgBWQ6 DIJ3550
has assertion: NP54761.RAVW3ZXZF1DLiXfNov3Ngul82Xvw0xuZgBWQ6 DIJ3550130 assertion
has provenance: NP54761.RAVW3ZXZF1DLiXfNov3Ngul82Xvw0xuZgBWQ6 DIJ3550130 provenance
has publication info: NP54761.RAVW3ZXZF1DLiXfNov3Ngul82Xvw0xuZgBWQ6 DIJ3550130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54761.RAVW3ZXZF1DLiXfNov3Ngul82Xvw0xuZgBWQ6 DIJ3550130 assertion
type: Assertion
description: [Mutation screening of the MEN1 gene has been recommended for patients who meet clinical criteria for MEN1 (at least two of the following: parathyroid hyperplasia, pancreatic endocrine tumour or pituitary adenoma) and those in whom a diagnosis of MEN1 is suspected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15670192
was generated by: ECO_0000203

NP54762.RAelkSf-8K6AOdzlf8WDJ0kJ9IBHq5zo0BAGJNlXB5Wo0
has assertion: NP54762.RAelkSf-8K6AOdzlf8WDJ0kJ9IBHq5zo0BAGJNlXB5Wo0130 assertion
has provenance: NP54762.RAelkSf-8K6AOdzlf8WDJ0kJ9IBHq5zo0BAGJNlXB5Wo0130 provenance
has publication info: NP54762.RAelkSf-8K6AOdzlf8WDJ0kJ9IBHq5zo0BAGJNlXB5Wo0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54762.RAelkSf-8K6AOdzlf8WDJ0kJ9IBHq5zo0BAGJNlXB5Wo0130 assertion
type: Assertion
description: [ The finding of MEN1 germ-line mutation in all patients with familial MEN1 syndrome suggests that genetic screening should be useful in our population to identify affected individuals within a kindred and allow early detection of MEN1-related tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12807514
was generated by: ECO_0000203

NP54767.RAVIRIrvXcOOprdJtYGe3xGSlL76zBfmRzTTTyNC2J1-c
has assertion: NP54767.RAVIRIrvXcOOprdJtYGe3xGSlL76zBfmRzTTTyNC2J1-c130 assertion
has provenance: NP54767.RAVIRIrvXcOOprdJtYGe3xGSlL76zBfmRzTTTyNC2J1-c130 provenance
has publication info: NP54767.RAVIRIrvXcOOprdJtYGe3xGSlL76zBfmRzTTTyNC2J1-c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54767.RAVIRIrvXcOOprdJtYGe3xGSlL76zBfmRzTTTyNC2J1-c130 assertion
type: Assertion
description: [Our study, based on a large group of MEN1 patients, shows that pituitary adenomas occur in 42% of the cases and are characterized by a larger size and a more aggressive presentation than without MEN1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11836268
was generated by: ECO_0000203

NP54769.RAULdvAUIWfpO80iSWoITwOY-XJD0Lw9PRXHQ9qlzboZo
has assertion: NP54769.RAULdvAUIWfpO80iSWoITwOY-XJD0Lw9PRXHQ9qlzboZo130 assertion
has provenance: NP54769.RAULdvAUIWfpO80iSWoITwOY-XJD0Lw9PRXHQ9qlzboZo130 provenance
has publication info: NP54769.RAULdvAUIWfpO80iSWoITwOY-XJD0Lw9PRXHQ9qlzboZo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54769.RAULdvAUIWfpO80iSWoITwOY-XJD0Lw9PRXHQ9qlzboZo130 assertion
type: Assertion
description: [More than 50 disease-associated mutations of the Mediterranean fever gene (MEFV) have been identified in familial Mediterranean fever (FMF), some of which were shown to have different clinical, diagnostic, prognostic, and therapeutic implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20008920
was generated by: ECO_0000203

NP54772.RAQakk s1k8ckYQNJwCc9oBFY3BSvFf0QtXn0q0cCi9-o
has assertion: NP54772.RAQakk s1k8ckYQNJwCc9oBFY3BSvFf0QtXn0q0cCi9-o130 assertion
has provenance: NP54772.RAQakk s1k8ckYQNJwCc9oBFY3BSvFf0QtXn0q0cCi9-o130 provenance
has publication info: NP54772.RAQakk s1k8ckYQNJwCc9oBFY3BSvFf0QtXn0q0cCi9-o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54772.RAQakk s1k8ckYQNJwCc9oBFY3BSvFf0QtXn0q0cCi9-o130 assertion
type: Assertion
description: [Familial mediterranean fever (FMF) is a hereditary autoinflammatory autosomal recessive disease caused by mutations in the MEFV gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18648395
was generated by: ECO_0000203

NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC dABEihIaskuwZU
has assertion: NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC dABEihIaskuwZU130 assertion
has provenance: NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC dABEihIaskuwZU130 provenance
has publication info: NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC dABEihIaskuwZU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC dABEihIaskuwZU130 assertion
type: Assertion
description: [To assess the protective as well as the modulating affect of MEFV mutation carriage on various inflammatory disease states, we sought to define the frequency of MEFV mutations in Israeli Jewish individuals of various ethnicities, including those with low frequency of FMF, which were not in the focus of our attention hitherto.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19373257
was generated by: ECO_0000203

NP54780.RAdiivFgnhKpMgCWJSQ Ewdk2NKrFH 4sLYSoVXlW-VQg
has assertion: NP54780.RAdiivFgnhKpMgCWJSQ Ewdk2NKrFH 4sLYSoVXlW-VQg130 assertion
has provenance: NP54780.RAdiivFgnhKpMgCWJSQ Ewdk2NKrFH 4sLYSoVXlW-VQg130 provenance
has publication info: NP54780.RAdiivFgnhKpMgCWJSQ Ewdk2NKrFH 4sLYSoVXlW-VQg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54780.RAdiivFgnhKpMgCWJSQ Ewdk2NKrFH 4sLYSoVXlW-VQg130 assertion
type: Assertion
description: [We investigated the hypothesis that low-penetrance mutations in genes (TNFRSF1A, MEFV and NALP3/CIAS1) associated with hereditary periodic fever syndromes (HPFs) might be risk factors for AA amyloidosis among patients with chronic inflammatory disorders, including rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), Crohn's disease, undiagnosed recurrent fevers and HPFs themselves.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15071491
was generated by: ECO_0000203

NP54782.RAdrCKyM4K-RZhX-TXHnLAdzek-lC2o43YlAZnh9VNDY4
has assertion: NP54782.RAdrCKyM4K-RZhX-TXHnLAdzek-lC2o43YlAZnh9VNDY4130 assertion
has provenance: NP54782.RAdrCKyM4K-RZhX-TXHnLAdzek-lC2o43YlAZnh9VNDY4130 provenance
has publication info: NP54782.RAdrCKyM4K-RZhX-TXHnLAdzek-lC2o43YlAZnh9VNDY4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54782.RAdrCKyM4K-RZhX-TXHnLAdzek-lC2o43YlAZnh9VNDY4130 assertion
type: Assertion
description: [Given that BD and FMF have similar pathophysiological, epidemiological, and clinical features, we hypothesized that the gene responsible for FMF, MEFV, may also play a role in the pathogenesis of BD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15903027
was generated by: ECO_0000203

NP54787.RARRH4BuE9UjWM0E7lPB-S5XBPp-zuFnxlDj5h13 QkI4
has assertion: NP54787.RARRH4BuE9UjWM0E7lPB-S5XBPp-zuFnxlDj5h13 QkI4130 assertion
has provenance: NP54787.RARRH4BuE9UjWM0E7lPB-S5XBPp-zuFnxlDj5h13 QkI4130 provenance
has publication info: NP54787.RARRH4BuE9UjWM0E7lPB-S5XBPp-zuFnxlDj5h13 QkI4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54787.RARRH4BuE9UjWM0E7lPB-S5XBPp-zuFnxlDj5h13 QkI4130 assertion
type: Assertion
description: [The association of the HOPA(12bp) polymorphism with schizophrenia in the NIMH Genetics Initiative for Schizophrenia sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17299734
was generated by: ECO_0000203

NP54791.RAat7lIJ3IUD1hk077T8hPmBWTf56gPwqkI8ud hgDo5A
has assertion: NP54791.RAat7lIJ3IUD1hk077T8hPmBWTf56gPwqkI8ud hgDo5A130 assertion
has provenance: NP54791.RAat7lIJ3IUD1hk077T8hPmBWTf56gPwqkI8ud hgDo5A130 provenance
has publication info: NP54791.RAat7lIJ3IUD1hk077T8hPmBWTf56gPwqkI8ud hgDo5A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54791.RAat7lIJ3IUD1hk077T8hPmBWTf56gPwqkI8ud hgDo5A130 assertion
type: Assertion
description: [In Chinese RTT patients, the MECP2 mutations are mostly of paternal origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20376788
was generated by: ECO_0000203

NP54793.RAfBU2wW5S7BbbXfoCAkE45b1ogSyocxfl oQ6vADLB0U
has assertion: NP54793.RAfBU2wW5S7BbbXfoCAkE45b1ogSyocxfl oQ6vADLB0U130 assertion
has provenance: NP54793.RAfBU2wW5S7BbbXfoCAkE45b1ogSyocxfl oQ6vADLB0U130 provenance
has publication info: NP54793.RAfBU2wW5S7BbbXfoCAkE45b1ogSyocxfl oQ6vADLB0U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54793.RAfBU2wW5S7BbbXfoCAkE45b1ogSyocxfl oQ6vADLB0U130 assertion
type: Assertion
description: [Through the use of post-PCR high-performance liquid chromatography, 65 percent of 20 RS patients were found to have mutation(s) in the MECP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19495527
was generated by: ECO_0000203

NP54797.RAYucTW17vvqT2njl1L1AEkE6-7RLOiBn7o9wmZoNJJps
has assertion: NP54797.RAYucTW17vvqT2njl1L1AEkE6-7RLOiBn7o9wmZoNJJps130 assertion
has provenance: NP54797.RAYucTW17vvqT2njl1L1AEkE6-7RLOiBn7o9wmZoNJJps130 provenance
has publication info: NP54797.RAYucTW17vvqT2njl1L1AEkE6-7RLOiBn7o9wmZoNJJps130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54797.RAYucTW17vvqT2njl1L1AEkE6-7RLOiBn7o9wmZoNJJps130 assertion
type: Assertion
description: [Novel exon 1 mutations in MECP2 implicate isoform MeCP2_e1 in classical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19365833
was generated by: ECO_0000203

NP54801.RAUF5wmshd8zKIQcM-H50BerixHR7-SFWJfC4qki8dd7A
has assertion: NP54801.RAUF5wmshd8zKIQcM-H50BerixHR7-SFWJfC4qki8dd7A130 assertion
has provenance: NP54801.RAUF5wmshd8zKIQcM-H50BerixHR7-SFWJfC4qki8dd7A130 provenance
has publication info: NP54801.RAUF5wmshd8zKIQcM-H50BerixHR7-SFWJfC4qki8dd7A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54801.RAUF5wmshd8zKIQcM-H50BerixHR7-SFWJfC4qki8dd7A130 assertion
type: Assertion
description: [The true frequency of MECP2 mutations in the mentally retarded has probably been overestimated. Based on our data, the frequency of MECP2 mutations in mentally retarded males is 0.2% (1/475).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12111644
was generated by: ECO_0000203

NP54802.RAYGyWibeBsA8KPONRi6JZoOtvOHo-Ms0zJpF-AIiJgpU
has assertion: NP54802.RAYGyWibeBsA8KPONRi6JZoOtvOHo-Ms0zJpF-AIiJgpU130 assertion
has provenance: NP54802.RAYGyWibeBsA8KPONRi6JZoOtvOHo-Ms0zJpF-AIiJgpU130 provenance
has publication info: NP54802.RAYGyWibeBsA8KPONRi6JZoOtvOHo-Ms0zJpF-AIiJgpU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54802.RAYGyWibeBsA8KPONRi6JZoOtvOHo-Ms0zJpF-AIiJgpU130 assertion
type: Assertion
description: [High frequency of nonrecurrent MECP2 duplications among Brazilian males with mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19806472
was generated by: ECO_0000203

NP54803.RAcV34aqZS9USZzJhOW34pmCMQZlgRnHSOs-d77Oq69AU
has assertion: NP54803.RAcV34aqZS9USZzJhOW34pmCMQZlgRnHSOs-d77Oq69AU130 assertion
has provenance: NP54803.RAcV34aqZS9USZzJhOW34pmCMQZlgRnHSOs-d77Oq69AU130 provenance
has publication info: NP54803.RAcV34aqZS9USZzJhOW34pmCMQZlgRnHSOs-d77Oq69AU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54803.RAcV34aqZS9USZzJhOW34pmCMQZlgRnHSOs-d77Oq69AU130 assertion
type: Assertion
description: [These results do not support previous evidence that genetic variation of the ME2 gene predisposes to common IGE syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16190936
was generated by: ECO_0000203

NP54815.RAUv7 RXbknBeIthi76xZSvk0iTi5NWu5763zaR5uFKPc
has assertion: NP54815.RAUv7 RXbknBeIthi76xZSvk0iTi5NWu5763zaR5uFKPc130 assertion
has provenance: NP54815.RAUv7 RXbknBeIthi76xZSvk0iTi5NWu5763zaR5uFKPc130 provenance
has publication info: NP54815.RAUv7 RXbknBeIthi76xZSvk0iTi5NWu5763zaR5uFKPc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54815.RAUv7 RXbknBeIthi76xZSvk0iTi5NWu5763zaR5uFKPc130 assertion
type: Assertion
description: [cumulative cigarette smoking plays a pivotal role in the association between mEH polymorphisms and lung cancer risk, altering the direction of risk (in the case of the very low activity genotype) from a risk factor in nonsmokers to a relatively protective factor in heavy smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11352855
was generated by: ECO_0000203

NP54816.RARhuxvKuV8YkrU9A1zRFiWJwEKJxOQwFt5tzTJRb85DU
has assertion: NP54816.RARhuxvKuV8YkrU9A1zRFiWJwEKJxOQwFt5tzTJRb85DU130 assertion
has provenance: NP54816.RARhuxvKuV8YkrU9A1zRFiWJwEKJxOQwFt5tzTJRb85DU130 provenance
has publication info: NP54816.RARhuxvKuV8YkrU9A1zRFiWJwEKJxOQwFt5tzTJRb85DU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54816.RARhuxvKuV8YkrU9A1zRFiWJwEKJxOQwFt5tzTJRb85DU130 assertion
type: Assertion
description: [Impact of the MDM2 SNP309 and p53 Arg72Pro polymorphism on age of tumour onset in Li-Fraumeni syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16258005
was generated by: ECO_0000203

NP54817.RATbDFSuP 3NwEAFb4ipCNGy OpCk9N0PiOTmDhcwzrBM
has assertion: NP54817.RATbDFSuP 3NwEAFb4ipCNGy OpCk9N0PiOTmDhcwzrBM130 assertion
has provenance: NP54817.RATbDFSuP 3NwEAFb4ipCNGy OpCk9N0PiOTmDhcwzrBM130 provenance
has publication info: NP54817.RATbDFSuP 3NwEAFb4ipCNGy OpCk9N0PiOTmDhcwzrBM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54817.RATbDFSuP 3NwEAFb4ipCNGy OpCk9N0PiOTmDhcwzrBM130 assertion
type: Assertion
description: [This study aimed to characterize the TP53 mutational spectrum in patients suspected to have LFS in Portugal and to evaluate the influence of the MDM2-SNP309 and TP53-72Arg variants and of telomere length on age of tumor onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19468865
was generated by: ECO_0000203

NP54818.RAYPFV iND9Cv5UPBl-npoa YvonDhOERThGH7zANYLoI
has assertion: NP54818.RAYPFV iND9Cv5UPBl-npoa YvonDhOERThGH7zANYLoI130 assertion
has provenance: NP54818.RAYPFV iND9Cv5UPBl-npoa YvonDhOERThGH7zANYLoI130 provenance
has publication info: NP54818.RAYPFV iND9Cv5UPBl-npoa YvonDhOERThGH7zANYLoI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54818.RAYPFV iND9Cv5UPBl-npoa YvonDhOERThGH7zANYLoI130 assertion
type: Assertion
description: [TP53 PIN3 and MDM2 SNP309 polymorphisms as genetic modifiers in the Li-Fraumeni syndrome: impact on age at first diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19542078
was generated by: ECO_0000203

NP54822.RASX0t4Egz4vlZcrEEPSH3xV6pCmctpMBJw4xyvb4zAbY
has assertion: NP54822.RASX0t4Egz4vlZcrEEPSH3xV6pCmctpMBJw4xyvb4zAbY130 assertion
has provenance: NP54822.RASX0t4Egz4vlZcrEEPSH3xV6pCmctpMBJw4xyvb4zAbY130 provenance
has publication info: NP54822.RASX0t4Egz4vlZcrEEPSH3xV6pCmctpMBJw4xyvb4zAbY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54822.RASX0t4Egz4vlZcrEEPSH3xV6pCmctpMBJw4xyvb4zAbY130 assertion
type: Assertion
description: [Combined effects of single nucleotide polymorphisms TP53 R72P and MDM2 SNP309, and p53 expression on survival of breast cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20021639
was generated by: ECO_0000203

NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM
has assertion: NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130 assertion
has provenance: NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130 provenance
has publication info: NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130 assertion
type: Assertion
description: [These results indicate an association between the presence of G at position minus sign2518 in the MCP-1 promoter region and the presence of cutaneous vasculitis among patients with SLE. This polymorphism does not seem to influence the susceptibility to SLE nor the appearance of lupus nephritis. Further studies are necessary in order to elucidate the role of this polymorphism in the pathogenesis of other inflammatory autoimmune diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11844145
was generated by: ECO_0000203

NP54842.RARhMj0pSJNTZwL6XI6YHAM-5NGua2cqyy5GtKhNIQD2o
has assertion: NP54842.RARhMj0pSJNTZwL6XI6YHAM-5NGua2cqyy5GtKhNIQD2o130 assertion
has provenance: NP54842.RARhMj0pSJNTZwL6XI6YHAM-5NGua2cqyy5GtKhNIQD2o130 provenance
has publication info: NP54842.RARhMj0pSJNTZwL6XI6YHAM-5NGua2cqyy5GtKhNIQD2o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54842.RARhMj0pSJNTZwL6XI6YHAM-5NGua2cqyy5GtKhNIQD2o130 assertion
type: Assertion
description: [In addition to FTO and MC4R, we detected significant association of obesity with three new risk loci in NPC1 (endosomal/lysosomal Niemann-Pick C1 gene, P = 2.9 x 10(-7)), near MAF (encoding the transcription factor c-MAF, P = 3.8 x 10(-13)) and near PTER (phosphotriesterase-related gene, P = 2.1 x 10(-7)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19151714
was generated by: ECO_0000203

NP54850.RAbOkizMAjc-UCp32r1Zj8Bfpua8ClB 9RDIr8WmIfGSA
has assertion: NP54850.RAbOkizMAjc-UCp32r1Zj8Bfpua8ClB 9RDIr8WmIfGSA130 assertion
has provenance: NP54850.RAbOkizMAjc-UCp32r1Zj8Bfpua8ClB 9RDIr8WmIfGSA130 provenance
has publication info: NP54850.RAbOkizMAjc-UCp32r1Zj8Bfpua8ClB 9RDIr8WmIfGSA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54850.RAbOkizMAjc-UCp32r1Zj8Bfpua8ClB 9RDIr8WmIfGSA130 assertion
type: Assertion
description: [The objective of this study was to identify genetic variants of the MC3R gene and determine its association with childhood obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17639020
was generated by: ECO_0000203

NP54851.RAYMSch1arPcGjT1UHE90bmRJ1inuk-5Wejtih2 1stig
has assertion: NP54851.RAYMSch1arPcGjT1UHE90bmRJ1inuk-5Wejtih2 1stig130 assertion
has provenance: NP54851.RAYMSch1arPcGjT1UHE90bmRJ1inuk-5Wejtih2 1stig130 provenance
has publication info: NP54851.RAYMSch1arPcGjT1UHE90bmRJ1inuk-5Wejtih2 1stig130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54851.RAYMSch1arPcGjT1UHE90bmRJ1inuk-5Wejtih2 1stig130 assertion
type: Assertion
description: [The risk of VVS is increased with proinflammatory genetic variants of IL1RN and MC1R, and combined genetic effects are associated with additive risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15305821
was generated by: ECO_0000203

NP54854.RAaaptsNRitQR6mM LHoTfu2ZRb1JLJ5BOyx85M-oY6Xo
has assertion: NP54854.RAaaptsNRitQR6mM LHoTfu2ZRb1JLJ5BOyx85M-oY6Xo130 assertion
has provenance: NP54854.RAaaptsNRitQR6mM LHoTfu2ZRb1JLJ5BOyx85M-oY6Xo130 provenance
has publication info: NP54854.RAaaptsNRitQR6mM LHoTfu2ZRb1JLJ5BOyx85M-oY6Xo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54854.RAaaptsNRitQR6mM LHoTfu2ZRb1JLJ5BOyx85M-oY6Xo130 assertion
type: Assertion
description: [Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19484507
was generated by: ECO_0000203

NP54856.RATWkPlPZ08ifg3RCx55O-5flaP1zC B3BCt7tgiJp-WA
has assertion: NP54856.RATWkPlPZ08ifg3RCx55O-5flaP1zC B3BCt7tgiJp-WA130 assertion
has provenance: NP54856.RATWkPlPZ08ifg3RCx55O-5flaP1zC B3BCt7tgiJp-WA130 provenance
has publication info: NP54856.RATWkPlPZ08ifg3RCx55O-5flaP1zC B3BCt7tgiJp-WA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54856.RATWkPlPZ08ifg3RCx55O-5flaP1zC B3BCt7tgiJp-WA130 assertion
type: Assertion
description: [Two MC1R germline variants, Arg151Cys and Asp294His, were significantly associated with melanoma in Sardinia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19799798
was generated by: ECO_0000203

NP54858.RAQ7pBhUo9PPlN4 IUXgUSTbk5XYk2c7YwMRpDhxAIwD8
has assertion: NP54858.RAQ7pBhUo9PPlN4 IUXgUSTbk5XYk2c7YwMRpDhxAIwD8130 assertion
has provenance: NP54858.RAQ7pBhUo9PPlN4 IUXgUSTbk5XYk2c7YwMRpDhxAIwD8130 provenance
has publication info: NP54858.RAQ7pBhUo9PPlN4 IUXgUSTbk5XYk2c7YwMRpDhxAIwD8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54858.RAQ7pBhUo9PPlN4 IUXgUSTbk5XYk2c7YwMRpDhxAIwD8130 assertion
type: Assertion
description: [MC1R variant alleles and malignant melanoma risk in Israel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19269164
was generated by: ECO_0000203

NP54863.RAfm0J9vJJTAylDor9AqF7DvbjZ7WOvXtV8f0l1GvdkUk
has assertion: NP54863.RAfm0J9vJJTAylDor9AqF7DvbjZ7WOvXtV8f0l1GvdkUk130 assertion
has provenance: NP54863.RAfm0J9vJJTAylDor9AqF7DvbjZ7WOvXtV8f0l1GvdkUk130 provenance
has publication info: NP54863.RAfm0J9vJJTAylDor9AqF7DvbjZ7WOvXtV8f0l1GvdkUk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54863.RAfm0J9vJJTAylDor9AqF7DvbjZ7WOvXtV8f0l1GvdkUk130 assertion
type: Assertion
description: [We investigated the effect of MC1R variants on melanoma using a large, international population-based study design with complete determination of all MC1R coding region variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16982779
was generated by: ECO_0000203

NP54866.RAUQkhuIBtQiImtvGU7 k-AR nInpOVWuQaL94SLlXlV8
has assertion: NP54866.RAUQkhuIBtQiImtvGU7 k-AR nInpOVWuQaL94SLlXlV8130 assertion
has provenance: NP54866.RAUQkhuIBtQiImtvGU7 k-AR nInpOVWuQaL94SLlXlV8130 provenance
has publication info: NP54866.RAUQkhuIBtQiImtvGU7 k-AR nInpOVWuQaL94SLlXlV8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54866.RAUQkhuIBtQiImtvGU7 k-AR nInpOVWuQaL94SLlXlV8130 assertion
type: Assertion
description: [These preliminary data suggest a role for these genes in MS pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15210908
was generated by: ECO_0000203

NP54875.RAdigniEpUb-eiKVQvB6WyNTcpyLSDNecG8iHoy4NPBqg
has assertion: NP54875.RAdigniEpUb-eiKVQvB6WyNTcpyLSDNecG8iHoy4NPBqg130 assertion
has provenance: NP54875.RAdigniEpUb-eiKVQvB6WyNTcpyLSDNecG8iHoy4NPBqg130 provenance
has publication info: NP54875.RAdigniEpUb-eiKVQvB6WyNTcpyLSDNecG8iHoy4NPBqg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54875.RAdigniEpUb-eiKVQvB6WyNTcpyLSDNecG8iHoy4NPBqg130 assertion
type: Assertion
description: [ Polymorphism of the MBP or another gene in its vicinity appears to contribute to the etiology of MS for the subgroups of DR4- and DR5-positive Italians and Russians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12939427
was generated by: ECO_0000203

NP54881.RAXaUoxn9qHjwfmQXePQe B4UgauZPAPFpzbwV22tjykc
has assertion: NP54881.RAXaUoxn9qHjwfmQXePQe B4UgauZPAPFpzbwV22tjykc130 assertion
has provenance: NP54881.RAXaUoxn9qHjwfmQXePQe B4UgauZPAPFpzbwV22tjykc130 provenance
has publication info: NP54881.RAXaUoxn9qHjwfmQXePQe B4UgauZPAPFpzbwV22tjykc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54881.RAXaUoxn9qHjwfmQXePQe B4UgauZPAPFpzbwV22tjykc130 assertion
type: Assertion
description: [ The results of the study suggest that genes may interact in ways that either synergize or modify the effect of a single genetic effect and imply that association studies must be interpreted within the genetic background of the populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12626795
was generated by: ECO_0000203

NP54883.RAYAkOH5A5vYUdrf6WIeK ZPU-Bp5JC4zDrEgUavikGKQ
has assertion: NP54883.RAYAkOH5A5vYUdrf6WIeK ZPU-Bp5JC4zDrEgUavikGKQ130 assertion
has provenance: NP54883.RAYAkOH5A5vYUdrf6WIeK ZPU-Bp5JC4zDrEgUavikGKQ130 provenance
has publication info: NP54883.RAYAkOH5A5vYUdrf6WIeK ZPU-Bp5JC4zDrEgUavikGKQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54883.RAYAkOH5A5vYUdrf6WIeK ZPU-Bp5JC4zDrEgUavikGKQ130 assertion
type: Assertion
description: [Genetic approaches to the investigation of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11981324
was generated by: ECO_0000203

NP54884.RAflx1re0fs7IrhGAt VJ wZCJp2X4ViIM6mKT8zReTZE
has assertion: NP54884.RAflx1re0fs7IrhGAt VJ wZCJp2X4ViIM6mKT8zReTZE130 assertion
has provenance: NP54884.RAflx1re0fs7IrhGAt VJ wZCJp2X4ViIM6mKT8zReTZE130 provenance
has publication info: NP54884.RAflx1re0fs7IrhGAt VJ wZCJp2X4ViIM6mKT8zReTZE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54884.RAflx1re0fs7IrhGAt VJ wZCJp2X4ViIM6mKT8zReTZE130 assertion
type: Assertion
description: [These data suggest that inflammation or an active immune response may induce an increased amount of HTLV-I-infected T cells, leading to a high provirus load.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12651071
was generated by: ECO_0000203

NP54885.RAaokBQzJbxfNiiW6 o0Ze2CSX 5QCF-5HCjpEGKCEFJI
has assertion: NP54885.RAaokBQzJbxfNiiW6 o0Ze2CSX 5QCF-5HCjpEGKCEFJI130 assertion
has provenance: NP54885.RAaokBQzJbxfNiiW6 o0Ze2CSX 5QCF-5HCjpEGKCEFJI130 provenance
has publication info: NP54885.RAaokBQzJbxfNiiW6 o0Ze2CSX 5QCF-5HCjpEGKCEFJI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54885.RAaokBQzJbxfNiiW6 o0Ze2CSX 5QCF-5HCjpEGKCEFJI130 assertion
type: Assertion
description: [Characterization of mannose-binding lectin gene polymorphism among human T-cell lymphotropic virus 1 and 2-infected asymptomatic subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16216673
was generated by: ECO_0000203

NP54891.RASf0uM9CaEYxihuJRGRf7o1LBzyQ3dzmlp hU0AAb4Bs
has assertion: NP54891.RASf0uM9CaEYxihuJRGRf7o1LBzyQ3dzmlp hU0AAb4Bs130 assertion
has provenance: NP54891.RASf0uM9CaEYxihuJRGRf7o1LBzyQ3dzmlp hU0AAb4Bs130 provenance
has publication info: NP54891.RASf0uM9CaEYxihuJRGRf7o1LBzyQ3dzmlp hU0AAb4Bs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54891.RASf0uM9CaEYxihuJRGRf7o1LBzyQ3dzmlp hU0AAb4Bs130 assertion
type: Assertion
description: [Our data do not support associations between the mannose-binding lectin allelic variants studied and clinical expression of systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20022898
was generated by: ECO_0000203

NP54892.RAdo40tKXGHVzXf574ynC9G5IGGue6w7PLjKAguyekTfQ
has assertion: NP54892.RAdo40tKXGHVzXf574ynC9G5IGGue6w7PLjKAguyekTfQ130 assertion
has provenance: NP54892.RAdo40tKXGHVzXf574ynC9G5IGGue6w7PLjKAguyekTfQ130 provenance
has publication info: NP54892.RAdo40tKXGHVzXf574ynC9G5IGGue6w7PLjKAguyekTfQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54892.RAdo40tKXGHVzXf574ynC9G5IGGue6w7PLjKAguyekTfQ130 assertion
type: Assertion
description: [Analysis of combinations of gene variants revealed that the strong association with SLE for HLA DR3-DQ2-C4AQ0 remained after combination with FcgammaRIIa R/R, FcgammaRIIIa F/F, and MBL-low (OR>2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15535834
was generated by: ECO_0000203

NP54894.RAQwYG 4c2OuncN6Mx25k3vkT Z2ThhqqePcMJs m7Xg0
has assertion: NP54894.RAQwYG 4c2OuncN6Mx25k3vkT Z2ThhqqePcMJs m7Xg0130 assertion
has provenance: NP54894.RAQwYG 4c2OuncN6Mx25k3vkT Z2ThhqqePcMJs m7Xg0130 provenance
has publication info: NP54894.RAQwYG 4c2OuncN6Mx25k3vkT Z2ThhqqePcMJs m7Xg0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54894.RAQwYG 4c2OuncN6Mx25k3vkT Z2ThhqqePcMJs m7Xg0130 assertion
type: Assertion
description: [Only in SLE patients fulfilling > or =4 ACR criteria an increased frequency of MBL variant alleles was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11781711
was generated by: ECO_0000203

NP54898.RAY-dbm-2tSY-BhIO5G2j788XIbMasgiof-oKH HYTHA4
has assertion: NP54898.RAY-dbm-2tSY-BhIO5G2j788XIbMasgiof-oKH HYTHA4130 assertion
has provenance: NP54898.RAY-dbm-2tSY-BhIO5G2j788XIbMasgiof-oKH HYTHA4130 provenance
has publication info: NP54898.RAY-dbm-2tSY-BhIO5G2j788XIbMasgiof-oKH HYTHA4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54898.RAY-dbm-2tSY-BhIO5G2j788XIbMasgiof-oKH HYTHA4130 assertion
type: Assertion
description: [We determined the -159T mutation of the CD14 gene, the 896G mutation of the toll-like receptor 4 gene, the 3020insC mutation of the NOD2 gene (NOD2-3020insC), the IL-6 174G/C promoter polymorphism (IL6-174G/C), and the mannose-binding lectin genotype and their association to the subsequent development of neonatal sepsis in a large cohort of very low birth weight (VLBW) infants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14739370
was generated by: ECO_0000203

NP54900.RAT1yo42cpZy2hNYxRcmR0BHWBjODBQPfyKr7EC6AU-i8
has assertion: NP54900.RAT1yo42cpZy2hNYxRcmR0BHWBjODBQPfyKr7EC6AU-i8130 assertion
has provenance: NP54900.RAT1yo42cpZy2hNYxRcmR0BHWBjODBQPfyKr7EC6AU-i8130 provenance
has publication info: NP54900.RAT1yo42cpZy2hNYxRcmR0BHWBjODBQPfyKr7EC6AU-i8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54900.RAT1yo42cpZy2hNYxRcmR0BHWBjODBQPfyKr7EC6AU-i8130 assertion
type: Assertion
description: [Common polymorphisms in critical genes of innate immunity do not contribute to the risk for chronic disseminated candidiasis in adult leukemia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16110781
was generated by: ECO_0000203

NP54911.RAW-pJgj8OYdQmBDe-I0S94S7daTDEwZMi2J9i5NoGzJg
has assertion: NP54911.RAW-pJgj8OYdQmBDe-I0S94S7daTDEwZMi2J9i5NoGzJg130 assertion
has provenance: NP54911.RAW-pJgj8OYdQmBDe-I0S94S7daTDEwZMi2J9i5NoGzJg130 provenance
has publication info: NP54911.RAW-pJgj8OYdQmBDe-I0S94S7daTDEwZMi2J9i5NoGzJg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54911.RAW-pJgj8OYdQmBDe-I0S94S7daTDEwZMi2J9i5NoGzJg130 assertion
type: Assertion
description: [As MBL2 gene polymorphism is associated to an increased susceptibility to infection, we aimed to determine genetic variations in the MBL2 gene in rheumatic heart disease (RHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17174748
was generated by: ECO_0000203

NP54913.RAZ-AJRz6iihsBYlONRy4iKIbHQC76fcBBp9zu3BTjg1k
has assertion: NP54913.RAZ-AJRz6iihsBYlONRy4iKIbHQC76fcBBp9zu3BTjg1k130 assertion
has provenance: NP54913.RAZ-AJRz6iihsBYlONRy4iKIbHQC76fcBBp9zu3BTjg1k130 provenance
has publication info: NP54913.RAZ-AJRz6iihsBYlONRy4iKIbHQC76fcBBp9zu3BTjg1k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54913.RAZ-AJRz6iihsBYlONRy4iKIbHQC76fcBBp9zu3BTjg1k130 assertion
type: Assertion
description: [Association of mannose-binding lectin genotype with cardiovascular abnormalities in Kawasaki disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12699957
was generated by: ECO_0000203

NP54917.RAU2eDGGasjR2IfVLN3iW3aKPbDOkIaf34wY40cfwIQ2k
has assertion: NP54917.RAU2eDGGasjR2IfVLN3iW3aKPbDOkIaf34wY40cfwIQ2k130 assertion
has provenance: NP54917.RAU2eDGGasjR2IfVLN3iW3aKPbDOkIaf34wY40cfwIQ2k130 provenance
has publication info: NP54917.RAU2eDGGasjR2IfVLN3iW3aKPbDOkIaf34wY40cfwIQ2k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54917.RAU2eDGGasjR2IfVLN3iW3aKPbDOkIaf34wY40cfwIQ2k130 assertion
type: Assertion
description: [Association of MBL gene polymorphisms with major bacterial infection in patients treated with high-dose chemotherapy and autologous PBSCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15674393
was generated by: ECO_0000203

NP54919.RAfCD5BZ-zRbf T33eDNDb1dVmFfTa6tHXkB35dzPrb4U
has assertion: NP54919.RAfCD5BZ-zRbf T33eDNDb1dVmFfTa6tHXkB35dzPrb4U130 assertion
has provenance: NP54919.RAfCD5BZ-zRbf T33eDNDb1dVmFfTa6tHXkB35dzPrb4U130 provenance
has publication info: NP54919.RAfCD5BZ-zRbf T33eDNDb1dVmFfTa6tHXkB35dzPrb4U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54919.RAfCD5BZ-zRbf T33eDNDb1dVmFfTa6tHXkB35dzPrb4U130 assertion
type: Assertion
description: [We evaluated whether women with vulvar vestibulitis syndrome (VVS) could be subdivided on the basis of genotyping the polymorphic mannose-binding lectin (MBL) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18166320
was generated by: ECO_0000203

NP54925.RATEng7nuu 2r-8c1xszMtYTcX9Jm4elOHfCEc14LzYTk
has assertion: NP54925.RATEng7nuu 2r-8c1xszMtYTcX9Jm4elOHfCEc14LzYTk130 assertion
has provenance: NP54925.RATEng7nuu 2r-8c1xszMtYTcX9Jm4elOHfCEc14LzYTk130 provenance
has publication info: NP54925.RATEng7nuu 2r-8c1xszMtYTcX9Jm4elOHfCEc14LzYTk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54925.RATEng7nuu 2r-8c1xszMtYTcX9Jm4elOHfCEc14LzYTk130 assertion
type: Assertion
description: [To determine whether variant alleles in the coding portion of the mannose-binding lectin (MBL) gene are associated with increased susceptibility to systemic lupus erythematosus (SLE) and concomitant infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10524686
was generated by: ECO_0000203

NP54926.RAdrXRFFLpIQoB ohtP-EVdtpocn1Y6SIvTCAPmxKoQFQ
has assertion: NP54926.RAdrXRFFLpIQoB ohtP-EVdtpocn1Y6SIvTCAPmxKoQFQ130 assertion
has provenance: NP54926.RAdrXRFFLpIQoB ohtP-EVdtpocn1Y6SIvTCAPmxKoQFQ130 provenance
has publication info: NP54926.RAdrXRFFLpIQoB ohtP-EVdtpocn1Y6SIvTCAPmxKoQFQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54926.RAdrXRFFLpIQoB ohtP-EVdtpocn1Y6SIvTCAPmxKoQFQ130 assertion
type: Assertion
description: [After a preliminary report associating these variations with coronary artery disease (CAD), we determined MBL genotypes in 3 American Indian communities experiencing an increased mortality and morbidity from CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14732744
was generated by: ECO_0000203

NP54929.RAdcN1Pr3Hlp0frdi6hTy8Og8wCqQwZzPWNRgs8FyYjz0
has assertion: NP54929.RAdcN1Pr3Hlp0frdi6hTy8Og8wCqQwZzPWNRgs8FyYjz0130 assertion
has provenance: NP54929.RAdcN1Pr3Hlp0frdi6hTy8Og8wCqQwZzPWNRgs8FyYjz0130 provenance
has publication info: NP54929.RAdcN1Pr3Hlp0frdi6hTy8Og8wCqQwZzPWNRgs8FyYjz0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54929.RAdcN1Pr3Hlp0frdi6hTy8Og8wCqQwZzPWNRgs8FyYjz0130 assertion
type: Assertion
description: [Single nucleotide polymorphisms of the mannose-binding lectin are associated with susceptibility to primary biliary cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11712863
was generated by: ECO_0000203

NP54933.RAcWCmzw4bBFu88CF8aY7uXbahjhwRX1Q5r1GAEpx0de0
has assertion: NP54933.RAcWCmzw4bBFu88CF8aY7uXbahjhwRX1Q5r1GAEpx0de0130 assertion
has provenance: NP54933.RAcWCmzw4bBFu88CF8aY7uXbahjhwRX1Q5r1GAEpx0de0130 provenance
has publication info: NP54933.RAcWCmzw4bBFu88CF8aY7uXbahjhwRX1Q5r1GAEpx0de0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54933.RAcWCmzw4bBFu88CF8aY7uXbahjhwRX1Q5r1GAEpx0de0130 assertion
type: Assertion
description: [ Our results demonstrate a role for the MBD2 gene in breast carcinogenesis in premenopausal women. These findings suggest that genetic variations in methylation related genes may potentially serve as a biomarker in risk estimates for breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16168120
was generated by: ECO_0000203

NP54937.RAcTIRRBwM4NysJCWGgpFu7c8yD5ygOql PzC2etyG-xc
has assertion: NP54937.RAcTIRRBwM4NysJCWGgpFu7c8yD5ygOql PzC2etyG-xc130 assertion
has provenance: NP54937.RAcTIRRBwM4NysJCWGgpFu7c8yD5ygOql PzC2etyG-xc130 provenance
has publication info: NP54937.RAcTIRRBwM4NysJCWGgpFu7c8yD5ygOql PzC2etyG-xc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54937.RAcTIRRBwM4NysJCWGgpFu7c8yD5ygOql PzC2etyG-xc130 assertion
type: Assertion
description: [However, when stratified on the +766C>T polymorphism of exon 3 of the LRP gene, the IB1/JIP-1 polymorphism was strongly associated with AD in subjects bearing the CC genotype in the LRP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12740599
was generated by: ECO_0000203

NP54939.RAeaOKoQAKoL Welg7o5NgRb1r7V6gW8m3w4hS-UBb9hE
has assertion: NP54939.RAeaOKoQAKoL Welg7o5NgRb1r7V6gW8m3w4hS-UBb9hE130 assertion
has provenance: NP54939.RAeaOKoQAKoL Welg7o5NgRb1r7V6gW8m3w4hS-UBb9hE130 provenance
has publication info: NP54939.RAeaOKoQAKoL Welg7o5NgRb1r7V6gW8m3w4hS-UBb9hE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54939.RAeaOKoQAKoL Welg7o5NgRb1r7V6gW8m3w4hS-UBb9hE130 assertion
type: Assertion
description: [Significant association was observed for monoamine oxidase-B(MAO-B) variant allele G and PD, whereas no difference in genotype and allele frequencies was observed for manganese-superoxide dismutase (MnSOD), dopamine receptor-D2(DRD2), and dopamine transporter (DAT) genes between controls and PD cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18327668
was generated by: ECO_0000203

NP54947.RAUTe5paK0I-wJfjnF6fKTWEc5tQ-6vvW4UlN5wwg2ha8
has assertion: NP54947.RAUTe5paK0I-wJfjnF6fKTWEc5tQ-6vvW4UlN5wwg2ha8130 assertion
has provenance: NP54947.RAUTe5paK0I-wJfjnF6fKTWEc5tQ-6vvW4UlN5wwg2ha8130 provenance
has publication info: NP54947.RAUTe5paK0I-wJfjnF6fKTWEc5tQ-6vvW4UlN5wwg2ha8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54947.RAUTe5paK0I-wJfjnF6fKTWEc5tQ-6vvW4UlN5wwg2ha8130 assertion
type: Assertion
description: [To investigate whether Parkinson's disease(PD) is associated with genetic polymorphism of intron 13 of monoamine oxidase B(MAO-B) and NAD(P)H: quinone oxidoreductase(NQO1) gene cDNA 609C to T.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11295131
was generated by: ECO_0000203

NP54950.RAfIsxCNEcBO-RkiMzp65L988xyt5FA9JcGHLUXWBtmcY
has assertion: NP54950.RAfIsxCNEcBO-RkiMzp65L988xyt5FA9JcGHLUXWBtmcY130 assertion
has provenance: NP54950.RAfIsxCNEcBO-RkiMzp65L988xyt5FA9JcGHLUXWBtmcY130 provenance
has publication info: NP54950.RAfIsxCNEcBO-RkiMzp65L988xyt5FA9JcGHLUXWBtmcY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54950.RAfIsxCNEcBO-RkiMzp65L988xyt5FA9JcGHLUXWBtmcY130 assertion
type: Assertion
description: [The distribution of selected polymorphic variants in the serotonin receptor type 2A and 1Dbeta (5-HT(2A), 5-HT(1Dbeta)), dopamine transporter (DAT), dopamine receptor type 4 (DRD4) and monoamine-oxidase A (MAO-A) genes were analysed in 71 OCD cases and 129 control individuals in the genetically homogeneous Afrikaner population, by means of case-control association studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12650952
was generated by: ECO_0000203

NP54951.RAfPFJp5uXUJjezSkCzBMkHGgnAv YkqCi7298Ls8cMbo
has assertion: NP54951.RAfPFJp5uXUJjezSkCzBMkHGgnAv YkqCi7298Ls8cMbo130 assertion
has provenance: NP54951.RAfPFJp5uXUJjezSkCzBMkHGgnAv YkqCi7298Ls8cMbo130 provenance
has publication info: NP54951.RAfPFJp5uXUJjezSkCzBMkHGgnAv YkqCi7298Ls8cMbo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54951.RAfPFJp5uXUJjezSkCzBMkHGgnAv YkqCi7298Ls8cMbo130 assertion
type: Assertion
description: [Additional evidence that genetic variation of MAO-A gene supports a gender subtype in obsessive-compulsive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11353450
was generated by: ECO_0000203

NP54953.RATp01oiPqFxspfRx jikjm4PdEe LvHhMte9XZi7RIiI
has assertion: NP54953.RATp01oiPqFxspfRx jikjm4PdEe LvHhMte9XZi7RIiI130 assertion
has provenance: NP54953.RATp01oiPqFxspfRx jikjm4PdEe LvHhMte9XZi7RIiI130 provenance
has publication info: NP54953.RATp01oiPqFxspfRx jikjm4PdEe LvHhMte9XZi7RIiI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54953.RATp01oiPqFxspfRx jikjm4PdEe LvHhMte9XZi7RIiI130 assertion
type: Assertion
description: [Thus, our data suggest that an excess of high-activity MAO-A gene promoter alleles resulting in an elevated MAO-A activity is a risk factor for major depressive disorder in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11121185
was generated by: ECO_0000203

NP54957.RAdXRdquPA-RjM8UeKVkZ6DUTR22xLTWk9ZVdhUaWoTH4
has assertion: NP54957.RAdXRdquPA-RjM8UeKVkZ6DUTR22xLTWk9ZVdhUaWoTH4130 assertion
has provenance: NP54957.RAdXRdquPA-RjM8UeKVkZ6DUTR22xLTWk9ZVdhUaWoTH4130 provenance
has publication info: NP54957.RAdXRdquPA-RjM8UeKVkZ6DUTR22xLTWk9ZVdhUaWoTH4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54957.RAdXRdquPA-RjM8UeKVkZ6DUTR22xLTWk9ZVdhUaWoTH4130 assertion
type: Assertion
description: [Our results provide fairly consistent evidence that high-activity variants of the MAOA promoter polymorphism confer a modestly higher risk for depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18626920
was generated by: ECO_0000203

NP54965.RAegmNBqalzlysOKYv7jwg85bQZocMsioKzJdDdd9GgzA
has assertion: NP54965.RAegmNBqalzlysOKYv7jwg85bQZocMsioKzJdDdd9GgzA130 assertion
has provenance: NP54965.RAegmNBqalzlysOKYv7jwg85bQZocMsioKzJdDdd9GgzA130 provenance
has publication info: NP54965.RAegmNBqalzlysOKYv7jwg85bQZocMsioKzJdDdd9GgzA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54965.RAegmNBqalzlysOKYv7jwg85bQZocMsioKzJdDdd9GgzA130 assertion
type: Assertion
description: [Relationship between the Fnu4HI site polymorphism of monoamine oxidase A gene and Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12778446
was generated by: ECO_0000203

NP54970.RAcxabmSLO74nO nitpr-Ewb8gDxoQfOtciaeurP lAqs
has assertion: NP54970.RAcxabmSLO74nO nitpr-Ewb8gDxoQfOtciaeurP lAqs130 assertion
has provenance: NP54970.RAcxabmSLO74nO nitpr-Ewb8gDxoQfOtciaeurP lAqs130 provenance
has publication info: NP54970.RAcxabmSLO74nO nitpr-Ewb8gDxoQfOtciaeurP lAqs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54970.RAcxabmSLO74nO nitpr-Ewb8gDxoQfOtciaeurP lAqs130 assertion
type: Assertion
description: [To ascertain whether mood disorders, including bipolar and unipolar, are genetically associated with the monoamine oxidase A (MAOA) or monoamine oxidase B (MAOB) gene in the Chinese population, 132 cases of mood disorder and 88 normal controls were genotyped for the MAOA(CA)n, MAOB(GT)n, and MAOB(TG)n loci by the method of amplification fragment length polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10686545
was generated by: ECO_0000203

NP54971.RAci2ZMesQhO3-Co-NE9wSVzMnL 8fNSPDhgFL9gAGgMM
has assertion: NP54971.RAci2ZMesQhO3-Co-NE9wSVzMnL 8fNSPDhgFL9gAGgMM130 assertion
has provenance: NP54971.RAci2ZMesQhO3-Co-NE9wSVzMnL 8fNSPDhgFL9gAGgMM130 provenance
has publication info: NP54971.RAci2ZMesQhO3-Co-NE9wSVzMnL 8fNSPDhgFL9gAGgMM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54971.RAci2ZMesQhO3-Co-NE9wSVzMnL 8fNSPDhgFL9gAGgMM130 assertion
type: Assertion
description: [Meta-analysis of the association between the monoamine oxidase-A gene and mood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20010318
was generated by: ECO_0000203

NP54974.RAdS2jBdC6QvcFPl7bvFtntiCQqdUBdU63MFPJs0yhoik
has assertion: NP54974.RAdS2jBdC6QvcFPl7bvFtntiCQqdUBdU63MFPJs0yhoik130 assertion
has provenance: NP54974.RAdS2jBdC6QvcFPl7bvFtntiCQqdUBdU63MFPJs0yhoik130 provenance
has publication info: NP54974.RAdS2jBdC6QvcFPl7bvFtntiCQqdUBdU63MFPJs0yhoik130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54974.RAdS2jBdC6QvcFPl7bvFtntiCQqdUBdU63MFPJs0yhoik130 assertion
type: Assertion
description: [These data suggest that functional genetic polymorphisms of the 5-HT system may influence the vulnerability to panic attacks and add to the growing evidence of inhibitory function of 5-HT in the neuronal circuitry of panic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15346539
was generated by: ECO_0000203

NP54977.RAZ1OXxHSO-n2v3yd--PG4PhmEuokZyqCdmudhPjFHL1w
has assertion: NP54977.RAZ1OXxHSO-n2v3yd--PG4PhmEuokZyqCdmudhPjFHL1w130 assertion
has provenance: NP54977.RAZ1OXxHSO-n2v3yd--PG4PhmEuokZyqCdmudhPjFHL1w130 provenance
has publication info: NP54977.RAZ1OXxHSO-n2v3yd--PG4PhmEuokZyqCdmudhPjFHL1w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54977.RAZ1OXxHSO-n2v3yd--PG4PhmEuokZyqCdmudhPjFHL1w130 assertion
type: Assertion
description: [Association studies of MAO-A, COMT, and 5-HTT genes polymorphisms in patients with anxiety disorders of the phobic spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15450911
was generated by: ECO_0000203

NP54981.RAZD7c5b-v7O6CSLC7tKSsQCxXP8--27RipJXXlhT-kKk
has assertion: NP54981.RAZD7c5b-v7O6CSLC7tKSsQCxXP8--27RipJXXlhT-kKk130 assertion
has provenance: NP54981.RAZD7c5b-v7O6CSLC7tKSsQCxXP8--27RipJXXlhT-kKk130 provenance
has publication info: NP54981.RAZD7c5b-v7O6CSLC7tKSsQCxXP8--27RipJXXlhT-kKk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54981.RAZD7c5b-v7O6CSLC7tKSsQCxXP8--27RipJXXlhT-kKk130 assertion
type: Assertion
description: [from others Brazilian studies with AD patients are also reported at this short review.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18607773
was generated by: ECO_0000203

NP54984.RARXkd7aNxg9A3pvsxvJ7EKO H1mf58MzDDmWDP5L58V0
has assertion: NP54984.RARXkd7aNxg9A3pvsxvJ7EKO H1mf58MzDDmWDP5L58V0130 assertion
has provenance: NP54984.RARXkd7aNxg9A3pvsxvJ7EKO H1mf58MzDDmWDP5L58V0130 provenance
has publication info: NP54984.RARXkd7aNxg9A3pvsxvJ7EKO H1mf58MzDDmWDP5L58V0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54984.RARXkd7aNxg9A3pvsxvJ7EKO H1mf58MzDDmWDP5L58V0130 assertion
type: Assertion
description: [Our results do not confirm the hypothesis that there is a simple correlation between single gene polymorphisms and a personality trait measured by the TCI and NEO-FFI scales.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15292674
was generated by: ECO_0000203

NP54988.RAUS5IOGedsHqwf4Of5jl8TsOX5f5fC7AoYt7l9WSAL1c
has assertion: NP54988.RAUS5IOGedsHqwf4Of5jl8TsOX5f5fC7AoYt7l9WSAL1c130 assertion
has provenance: NP54988.RAUS5IOGedsHqwf4Of5jl8TsOX5f5fC7AoYt7l9WSAL1c130 provenance
has publication info: NP54988.RAUS5IOGedsHqwf4Of5jl8TsOX5f5fC7AoYt7l9WSAL1c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54988.RAUS5IOGedsHqwf4Of5jl8TsOX5f5fC7AoYt7l9WSAL1c130 assertion
type: Assertion
description: [Association study between schizophrenia and monoamine oxidase A and B DNA polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/8804132
was generated by: ECO_0000203

NP54998.RAX8zElWiY46Xm EKfPpnOvp1rQpUx5xO7Cm T7c0NmE
has assertion: NP54998.RAX8zElWiY46Xm EKfPpnOvp1rQpUx5xO7Cm T7c0NmE130 assertion
has provenance: NP54998.RAX8zElWiY46Xm EKfPpnOvp1rQpUx5xO7Cm T7c0NmE130 provenance
has publication info: NP54998.RAX8zElWiY46Xm EKfPpnOvp1rQpUx5xO7Cm T7c0NmE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54998.RAX8zElWiY46Xm EKfPpnOvp1rQpUx5xO7Cm T7c0NmE130 assertion
type: Assertion
description: [Our results indicate that MAO-A may play a role in the development of alcoholism but the gene effect is very small.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12555234
was generated by: ECO_0000203

NP54999.RAYVjF5AFfLrkB6A9FTWBcQCquqe8Wo4KaG8KQJ-LcJP8
has assertion: NP54999.RAYVjF5AFfLrkB6A9FTWBcQCquqe8Wo4KaG8KQJ-LcJP8130 assertion
has provenance: NP54999.RAYVjF5AFfLrkB6A9FTWBcQCquqe8Wo4KaG8KQJ-LcJP8130 provenance
has publication info: NP54999.RAYVjF5AFfLrkB6A9FTWBcQCquqe8Wo4KaG8KQJ-LcJP8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP54999.RAYVjF5AFfLrkB6A9FTWBcQCquqe8Wo4KaG8KQJ-LcJP8130 assertion
type: Assertion
description: [Our results suggest that this monoamine oxidase A polymorphism could play a role in susceptibility to alcoholism, which may differ across sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15900229
was generated by: ECO_0000203

NP55014.RAVZJogYpGz6rrYOfF3i8qqz1uQbRDK-qaLrfcttOYFpw
has assertion: NP55014.RAVZJogYpGz6rrYOfF3i8qqz1uQbRDK-qaLrfcttOYFpw130 assertion
has provenance: NP55014.RAVZJogYpGz6rrYOfF3i8qqz1uQbRDK-qaLrfcttOYFpw130 provenance
has publication info: NP55014.RAVZJogYpGz6rrYOfF3i8qqz1uQbRDK-qaLrfcttOYFpw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55014.RAVZJogYpGz6rrYOfF3i8qqz1uQbRDK-qaLrfcttOYFpw130 assertion
type: Assertion
description: [These results support the hypothesis that binge drinking behavior in young adulthood may be influenced by neurobiological differences in serotonergic function conferred by functional polymorphisms in genes involved in serotonin processing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15635592
was generated by: ECO_0000203

NP55021.RAW2xUDu0oDieb5WWbxzqtvs Ad3ljXJ0VosQBpWGKf0I
has assertion: NP55021.RAW2xUDu0oDieb5WWbxzqtvs Ad3ljXJ0VosQBpWGKf0I130 assertion
has provenance: NP55021.RAW2xUDu0oDieb5WWbxzqtvs Ad3ljXJ0VosQBpWGKf0I130 provenance
has publication info: NP55021.RAW2xUDu0oDieb5WWbxzqtvs Ad3ljXJ0VosQBpWGKf0I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55021.RAW2xUDu0oDieb5WWbxzqtvs Ad3ljXJ0VosQBpWGKf0I130 assertion
type: Assertion
description: [The long-repeat allelic variants (>4-repeats) and 2-repeat allele of the DRD4 exon 3 VNTR polymorphism might be risk alleles for individual vulnerability to heroin addiction in Chinese men, but the MAOA promoter VNTR polymorphism does not mean that the partial dominant inherited mode might involved in the genetics of heroin dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20218801
was generated by: ECO_0000203

NP55022.RAV5Om5TxvIgEkEBx3QeCJ1JF90cXV9Z94-wBOpHwp1So
has assertion: NP55022.RAV5Om5TxvIgEkEBx3QeCJ1JF90cXV9Z94-wBOpHwp1So130 assertion
has provenance: NP55022.RAV5Om5TxvIgEkEBx3QeCJ1JF90cXV9Z94-wBOpHwp1So130 provenance
has publication info: NP55022.RAV5Om5TxvIgEkEBx3QeCJ1JF90cXV9Z94-wBOpHwp1So130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55022.RAV5Om5TxvIgEkEBx3QeCJ1JF90cXV9Z94-wBOpHwp1So130 assertion
type: Assertion
description: [Association of autism severity with a monoamine oxidase A functional polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12919132
was generated by: ECO_0000203

NP55032.RASYHSP6ANWqs8helgsXJeBcS9YmOxoJHXdk-iq6ku36w
has assertion: NP55032.RASYHSP6ANWqs8helgsXJeBcS9YmOxoJHXdk-iq6ku36w130 assertion
has provenance: NP55032.RASYHSP6ANWqs8helgsXJeBcS9YmOxoJHXdk-iq6ku36w130 provenance
has publication info: NP55032.RASYHSP6ANWqs8helgsXJeBcS9YmOxoJHXdk-iq6ku36w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55032.RASYHSP6ANWqs8helgsXJeBcS9YmOxoJHXdk-iq6ku36w130 assertion
type: Assertion
description: [All three complementary approaches employed (family-based, case-control and quantitative trait design) suggest a role for the MAO A promoter-region polymorphism in conferring risk for ADHD in our patient population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12140786
was generated by: ECO_0000203

NP55033.RAfchbbngtNaXxqtaUcSS3hImxyf2FP1MB4K QuBRhO-g
has assertion: NP55033.RAfchbbngtNaXxqtaUcSS3hImxyf2FP1MB4K QuBRhO-g130 assertion
has provenance: NP55033.RAfchbbngtNaXxqtaUcSS3hImxyf2FP1MB4K QuBRhO-g130 provenance
has publication info: NP55033.RAfchbbngtNaXxqtaUcSS3hImxyf2FP1MB4K QuBRhO-g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55033.RAfchbbngtNaXxqtaUcSS3hImxyf2FP1MB4K QuBRhO-g130 assertion
type: Assertion
description: [the short 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16856146
was generated by: ECO_0000203

NP55035.RAWkAhtfrItcHS4C 7s7nMnqD67WtGBz0k8Srz0eJzp7Q
has assertion: NP55035.RAWkAhtfrItcHS4C 7s7nMnqD67WtGBz0k8Srz0eJzp7Q130 assertion
has provenance: NP55035.RAWkAhtfrItcHS4C 7s7nMnqD67WtGBz0k8Srz0eJzp7Q130 provenance
has publication info: NP55035.RAWkAhtfrItcHS4C 7s7nMnqD67WtGBz0k8Srz0eJzp7Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55035.RAWkAhtfrItcHS4C 7s7nMnqD67WtGBz0k8Srz0eJzp7Q130 assertion
type: Assertion
description: [Monoamine oxidase A gene polymorphism predicts adolescent outcome of attention-deficit/hyperactivity disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17427196
was generated by: ECO_0000203

NP55046.RAVv6bm5VOMRPXM9pBTIWvtgXVkwyjM eZKXrYPheTb6A
has assertion: NP55046.RAVv6bm5VOMRPXM9pBTIWvtgXVkwyjM eZKXrYPheTb6A130 assertion
has provenance: NP55046.RAVv6bm5VOMRPXM9pBTIWvtgXVkwyjM eZKXrYPheTb6A130 provenance
has publication info: NP55046.RAVv6bm5VOMRPXM9pBTIWvtgXVkwyjM eZKXrYPheTb6A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55046.RAVv6bm5VOMRPXM9pBTIWvtgXVkwyjM eZKXrYPheTb6A130 assertion
type: Assertion
description: [Genetic association between monoamine oxidase A microsatellite and RFLP alleles and bipolar affective disorder: analysis and meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/8776592
was generated by: ECO_0000203

NP55052.RAZmibvYlxhOTNcR 2xM-lmvF7sv6jfosO8G8Ddk8k3rs
has assertion: NP55052.RAZmibvYlxhOTNcR 2xM-lmvF7sv6jfosO8G8Ddk8k3rs130 assertion
has provenance: NP55052.RAZmibvYlxhOTNcR 2xM-lmvF7sv6jfosO8G8Ddk8k3rs130 provenance
has publication info: NP55052.RAZmibvYlxhOTNcR 2xM-lmvF7sv6jfosO8G8Ddk8k3rs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55052.RAZmibvYlxhOTNcR 2xM-lmvF7sv6jfosO8G8Ddk8k3rs130 assertion
type: Assertion
description: [Genetic association between monoamine oxidase A microsatellite and RFLP alleles and bipolar affective disorder: analysis and meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/8776592
was generated by: ECO_0000203

NP55053.RAROztoEoQQ9YoFo5S9zTBUczrt99Y2uw1-sdmlTBZWwU
has assertion: NP55053.RAROztoEoQQ9YoFo5S9zTBUczrt99Y2uw1-sdmlTBZWwU130 assertion
has provenance: NP55053.RAROztoEoQQ9YoFo5S9zTBUczrt99Y2uw1-sdmlTBZWwU130 provenance
has publication info: NP55053.RAROztoEoQQ9YoFo5S9zTBUczrt99Y2uw1-sdmlTBZWwU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55053.RAROztoEoQQ9YoFo5S9zTBUczrt99Y2uw1-sdmlTBZWwU130 assertion
type: Assertion
description: [Genetic association between monoamine oxidase A microsatellite and RFLP alleles and bipolar affective disorder: analysis and meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/8776592
was generated by: ECO_0000203

NP55054.RAWgp2x5U2ePPrrRkFqApqtemk5OfCIfP8wTq-LEWHLnI
has assertion: NP55054.RAWgp2x5U2ePPrrRkFqApqtemk5OfCIfP8wTq-LEWHLnI130 assertion
has provenance: NP55054.RAWgp2x5U2ePPrrRkFqApqtemk5OfCIfP8wTq-LEWHLnI130 provenance
has publication info: NP55054.RAWgp2x5U2ePPrrRkFqApqtemk5OfCIfP8wTq-LEWHLnI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55054.RAWgp2x5U2ePPrrRkFqApqtemk5OfCIfP8wTq-LEWHLnI130 assertion
type: Assertion
description: [Genetic association between monoamine oxidase A microsatellite and RFLP alleles and bipolar affective disorder: analysis and meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/8776592
was generated by: ECO_0000203

NP55058.RAdgfZmNi0IBKwjsTTJm8Y3mA4ujWsDbesr8-kkuPI8oo
has assertion: NP55058.RAdgfZmNi0IBKwjsTTJm8Y3mA4ujWsDbesr8-kkuPI8oo130 assertion
has provenance: NP55058.RAdgfZmNi0IBKwjsTTJm8Y3mA4ujWsDbesr8-kkuPI8oo130 provenance
has publication info: NP55058.RAdgfZmNi0IBKwjsTTJm8Y3mA4ujWsDbesr8-kkuPI8oo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55058.RAdgfZmNi0IBKwjsTTJm8Y3mA4ujWsDbesr8-kkuPI8oo130 assertion
type: Assertion
description: [Where possible, asthma severity scores were assigned, ALOX5AP G-336A, ALOX5 G-1708A, LTC4S A-444C and G-1072A, GPX4 C718T, and CYSTLTR1 T927C genotypes were determined and uLTE(4) was measured in acute and convalescent samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19524426
was generated by: ECO_0000203

NP55065.RASF8lJNNFc 7 AEUy3DDt9qr5efGVUGOqtdpGYC0h9C4
has assertion: NP55065.RASF8lJNNFc 7 AEUy3DDt9qr5efGVUGOqtdpGYC0h9C4130 assertion
has provenance: NP55065.RASF8lJNNFc 7 AEUy3DDt9qr5efGVUGOqtdpGYC0h9C4130 provenance
has publication info: NP55065.RASF8lJNNFc 7 AEUy3DDt9qr5efGVUGOqtdpGYC0h9C4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55065.RASF8lJNNFc 7 AEUy3DDt9qr5efGVUGOqtdpGYC0h9C4130 assertion
type: Assertion
description: [The relevance of leukotriene C(4) synthase gene A (-444) C polymorphism to clinical responsiveness to montelukast in patients with asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19080532
was generated by: ECO_0000203

NP55068.RAf0pvJ7Fd9f1F9F2MNuZRyaIybloGFl efwdbVFtNE44
has assertion: NP55068.RAf0pvJ7Fd9f1F9F2MNuZRyaIybloGFl efwdbVFtNE44130 assertion
has provenance: NP55068.RAf0pvJ7Fd9f1F9F2MNuZRyaIybloGFl efwdbVFtNE44130 provenance
has publication info: NP55068.RAf0pvJ7Fd9f1F9F2MNuZRyaIybloGFl efwdbVFtNE44130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55068.RAf0pvJ7Fd9f1F9F2MNuZRyaIybloGFl efwdbVFtNE44130 assertion
type: Assertion
description: [The sorted genes allow us to draw novel hypotheses for future studies of HCV infection to ultimately identify bona fide genes and their variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15063762
was generated by: ECO_0000203

NP55073.RAfiNVADeYKXjLot2-ehMlTwcj9-R0m7EN4EQfO2xGMcU
has assertion: NP55073.RAfiNVADeYKXjLot2-ehMlTwcj9-R0m7EN4EQfO2xGMcU130 assertion
has provenance: NP55073.RAfiNVADeYKXjLot2-ehMlTwcj9-R0m7EN4EQfO2xGMcU130 provenance
has publication info: NP55073.RAfiNVADeYKXjLot2-ehMlTwcj9-R0m7EN4EQfO2xGMcU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55073.RAfiNVADeYKXjLot2-ehMlTwcj9-R0m7EN4EQfO2xGMcU130 assertion
type: Assertion
description: [We genotyped 26 SNPs that had previously been interrogated for association with montelukast response in five candidate genes (ABCC1, ALOX5, CYSLTR1, LTA4H, LTC4S) in a population of 577 asthmatics who participated in a clinical trial comparing intermittent and continuous-release zileuton to placebo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19214143
was generated by: ECO_0000203

NP55077.RAaEEdhP2EUeMEedizNTvHXq6hqi-Zt Eh1J5yb nLdBc
has assertion: NP55077.RAaEEdhP2EUeMEedizNTvHXq6hqi-Zt Eh1J5yb nLdBc130 assertion
has provenance: NP55077.RAaEEdhP2EUeMEedizNTvHXq6hqi-Zt Eh1J5yb nLdBc130 provenance
has publication info: NP55077.RAaEEdhP2EUeMEedizNTvHXq6hqi-Zt Eh1J5yb nLdBc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55077.RAaEEdhP2EUeMEedizNTvHXq6hqi-Zt Eh1J5yb nLdBc130 assertion
type: Assertion
description: [ The data suggest that genetic determinants of response to infliximab therapy exist in the HLA complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15077289
was generated by: ECO_0000203

NP55082.RAbOWNJlx2Mad2mCDJlwBXYa0iFY6D4KlEo81vZC24tmk
has assertion: NP55082.RAbOWNJlx2Mad2mCDJlwBXYa0iFY6D4KlEo81vZC24tmk130 assertion
has provenance: NP55082.RAbOWNJlx2Mad2mCDJlwBXYa0iFY6D4KlEo81vZC24tmk130 provenance
has publication info: NP55082.RAbOWNJlx2Mad2mCDJlwBXYa0iFY6D4KlEo81vZC24tmk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55082.RAbOWNJlx2Mad2mCDJlwBXYa0iFY6D4KlEo81vZC24tmk130 assertion
type: Assertion
description: [Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18636124
was generated by: ECO_0000203

NP55084.RAbtc zAAbMgKxnCpGMVSEb0btuxYb6697-zMthuukyXA
has assertion: NP55084.RAbtc zAAbMgKxnCpGMVSEb0btuxYb6697-zMthuukyXA130 assertion
has provenance: NP55084.RAbtc zAAbMgKxnCpGMVSEb0btuxYb6697-zMthuukyXA130 provenance
has publication info: NP55084.RAbtc zAAbMgKxnCpGMVSEb0btuxYb6697-zMthuukyXA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55084.RAbtc zAAbMgKxnCpGMVSEb0btuxYb6697-zMthuukyXA130 assertion
type: Assertion
description: [Haplotype-specific pattern of association of human major histocompatibility complex with non-Hodgkin's lymphoma outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17971052
was generated by: ECO_0000203

NP55087.RASPS-aMdJl1CFTKmgx339tXGDi1EjdgmcyXUWRCXomUI
has assertion: NP55087.RASPS-aMdJl1CFTKmgx339tXGDi1EjdgmcyXUWRCXomUI130 assertion
has provenance: NP55087.RASPS-aMdJl1CFTKmgx339tXGDi1EjdgmcyXUWRCXomUI130 provenance
has publication info: NP55087.RASPS-aMdJl1CFTKmgx339tXGDi1EjdgmcyXUWRCXomUI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55087.RASPS-aMdJl1CFTKmgx339tXGDi1EjdgmcyXUWRCXomUI130 assertion
type: Assertion
description: [Systemic lupus erythematosus with nephritis is strongly associated with the TNFB*2 homozygote in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9157084
was generated by: ECO_0000203

NP55088.RAYgDAiHdAfoAc6Y7k8T9IoEj-YUX7pEPodFPIC5RFsZw
has assertion: NP55088.RAYgDAiHdAfoAc6Y7k8T9IoEj-YUX7pEPodFPIC5RFsZw130 assertion
has provenance: NP55088.RAYgDAiHdAfoAc6Y7k8T9IoEj-YUX7pEPodFPIC5RFsZw130 provenance
has publication info: NP55088.RAYgDAiHdAfoAc6Y7k8T9IoEj-YUX7pEPodFPIC5RFsZw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55088.RAYgDAiHdAfoAc6Y7k8T9IoEj-YUX7pEPodFPIC5RFsZw130 assertion
type: Assertion
description: [These data suggest that inflammation or an active immune response may induce an increased amount of HTLV-I-infected T cells, leading to a high provirus load.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12651071
was generated by: ECO_0000203

NP55089.RAdDbD9ZrB-EAAkfat-CSBH0EGxTBaTWHhFvzjLGrHmik
has assertion: NP55089.RAdDbD9ZrB-EAAkfat-CSBH0EGxTBaTWHhFvzjLGrHmik130 assertion
has provenance: NP55089.RAdDbD9ZrB-EAAkfat-CSBH0EGxTBaTWHhFvzjLGrHmik130 provenance
has publication info: NP55089.RAdDbD9ZrB-EAAkfat-CSBH0EGxTBaTWHhFvzjLGrHmik130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55089.RAdDbD9ZrB-EAAkfat-CSBH0EGxTBaTWHhFvzjLGrHmik130 assertion
type: Assertion
description: [We adapted template-directed dye-terminator incorporation with fluorescence polarization detection (TDI-FP) to the analysis of eight SNPs implicated in mediating the sepsis syndrome: TNF-alpha (-308), TNF-alpha (-238), TNF-beta (+250), IL-1beta (+3953), IL-6 (-174), IL-10 (-592), plasminogen activator inhibitor-1 (PAI-1 (-675)), and TLR4 299 (+1032).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12411588
was generated by: ECO_0000203

NP55090.RAdfK2O6Zi0Eso6YMzTcGcAErF-TBFkraSjAKzLZJOLWA
has assertion: NP55090.RAdfK2O6Zi0Eso6YMzTcGcAErF-TBFkraSjAKzLZJOLWA130 assertion
has provenance: NP55090.RAdfK2O6Zi0Eso6YMzTcGcAErF-TBFkraSjAKzLZJOLWA130 provenance
has publication info: NP55090.RAdfK2O6Zi0Eso6YMzTcGcAErF-TBFkraSjAKzLZJOLWA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55090.RAdfK2O6Zi0Eso6YMzTcGcAErF-TBFkraSjAKzLZJOLWA130 assertion
type: Assertion
description: [ Microsatellite TNFa is significantly associated with both the susceptibility to and outcome of severe sepsis. In contrast, microsatellite TNFb is neither associated with the susceptibility to severe sepsis nor with the outcome of severe sepsis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12126516
was generated by: ECO_0000203

NP55092.RAXZarvEE5H Qs1WuzNgTg3IROi6tzeZHwHFhJR u9snU
has assertion: NP55092.RAXZarvEE5H Qs1WuzNgTg3IROi6tzeZHwHFhJR u9snU130 assertion
has provenance: NP55092.RAXZarvEE5H Qs1WuzNgTg3IROi6tzeZHwHFhJR u9snU130 provenance
has publication info: NP55092.RAXZarvEE5H Qs1WuzNgTg3IROi6tzeZHwHFhJR u9snU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55092.RAXZarvEE5H Qs1WuzNgTg3IROi6tzeZHwHFhJR u9snU130 assertion
type: Assertion
description: [In severe sepsis, tumor necrosis factor-beta (TNF-beta) NcoI polymorphism was associated with increased mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15041959
was generated by: ECO_0000203

NP55097.RAa8nQwhTWmznY1kTcoqOWbyzXL2xBh54mKkmPivmJ1uk
has assertion: NP55097.RAa8nQwhTWmznY1kTcoqOWbyzXL2xBh54mKkmPivmJ1uk130 assertion
has provenance: NP55097.RAa8nQwhTWmznY1kTcoqOWbyzXL2xBh54mKkmPivmJ1uk130 provenance
has publication info: NP55097.RAa8nQwhTWmznY1kTcoqOWbyzXL2xBh54mKkmPivmJ1uk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55097.RAa8nQwhTWmznY1kTcoqOWbyzXL2xBh54mKkmPivmJ1uk130 assertion
type: Assertion
description: [These results suggest donor TNFalpha-857 CC genotype is related to a higher incidence of grade II-IV aGVHD, and patients with TNFbeta + 252 AA genotype have protection against the risk of grade II-IV aGVHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20627040
was generated by: ECO_0000203

NP55100.RARpe9QycJxEMwmpUUcNWMUjdxuPut7tINsq7RQ0BpsaU
has assertion: NP55100.RARpe9QycJxEMwmpUUcNWMUjdxuPut7tINsq7RQ0BpsaU130 assertion
has provenance: NP55100.RARpe9QycJxEMwmpUUcNWMUjdxuPut7tINsq7RQ0BpsaU130 provenance
has publication info: NP55100.RARpe9QycJxEMwmpUUcNWMUjdxuPut7tINsq7RQ0BpsaU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55100.RARpe9QycJxEMwmpUUcNWMUjdxuPut7tINsq7RQ0BpsaU130 assertion
type: Assertion
description: [In an effort to discover polymorphism(s) in genes whose variant(s) have been implicated in asthma phenotypes, we examined the genetic effects of TNF (TNFA and TNFB) polymorphisms on asthma and total serum IgE level.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14681301
was generated by: ECO_0000203

NP55102.RAUzpXgD8PtaXGFzu-5yMQ2Us-0K G Dtk3ixNaQGgwcE
has assertion: NP55102.RAUzpXgD8PtaXGFzu-5yMQ2Us-0K G Dtk3ixNaQGgwcE130 assertion
has provenance: NP55102.RAUzpXgD8PtaXGFzu-5yMQ2Us-0K G Dtk3ixNaQGgwcE130 provenance
has publication info: NP55102.RAUzpXgD8PtaXGFzu-5yMQ2Us-0K G Dtk3ixNaQGgwcE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55102.RAUzpXgD8PtaXGFzu-5yMQ2Us-0K G Dtk3ixNaQGgwcE130 assertion
type: Assertion
description: [Gene-gene synergistic effect on atopic asthma: tumour necrosis factor-alpha-308 and lymphotoxin-alpha-NcoI in Taiwan's children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14987295
was generated by: ECO_0000203

NP55104.RAcQGp3kEvIEHyYT4C68djX9320dz4Rl5VT2c9gbIiubs
has assertion: NP55104.RAcQGp3kEvIEHyYT4C68djX9320dz4Rl5VT2c9gbIiubs130 assertion
has provenance: NP55104.RAcQGp3kEvIEHyYT4C68djX9320dz4Rl5VT2c9gbIiubs130 provenance
has publication info: NP55104.RAcQGp3kEvIEHyYT4C68djX9320dz4Rl5VT2c9gbIiubs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55104.RAcQGp3kEvIEHyYT4C68djX9320dz4Rl5VT2c9gbIiubs130 assertion
type: Assertion
description: [To investigate the association of differences in asthma-related phenotypes with two biallelic polymorphisms: a G to A substitution at position - 308 of the TNFalpha gene promoter (TNF1 and TNF2 alleles) and an NcoI polymorphism in the first intron of the lymphotoxin alpha gene (LT-alpha*1 and LT-alpha*2 alleles).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9645594
was generated by: ECO_0000203

NP55106.RAXuBxYVbwHW7uVCg2RGKi39JyC84P-3C5sFQv8 RacKc
has assertion: NP55106.RAXuBxYVbwHW7uVCg2RGKi39JyC84P-3C5sFQv8 RacKc130 assertion
has provenance: NP55106.RAXuBxYVbwHW7uVCg2RGKi39JyC84P-3C5sFQv8 RacKc130 provenance
has publication info: NP55106.RAXuBxYVbwHW7uVCg2RGKi39JyC84P-3C5sFQv8 RacKc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55106.RAXuBxYVbwHW7uVCg2RGKi39JyC84P-3C5sFQv8 RacKc130 assertion
type: Assertion
description: [Association of a lymphotoxin-alpha gene polymorphism and atopic asthma in Taiwanese children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18947013
was generated by: ECO_0000203

NP55109.RAezszimqUIJVlFBw6Q57VRcPSMA4 V6NIGQSDcI-OsF8
has assertion: NP55109.RAezszimqUIJVlFBw6Q57VRcPSMA4 V6NIGQSDcI-OsF8130 assertion
has provenance: NP55109.RAezszimqUIJVlFBw6Q57VRcPSMA4 V6NIGQSDcI-OsF8130 provenance
has publication info: NP55109.RAezszimqUIJVlFBw6Q57VRcPSMA4 V6NIGQSDcI-OsF8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55109.RAezszimqUIJVlFBw6Q57VRcPSMA4 V6NIGQSDcI-OsF8130 assertion
type: Assertion
description: [ The data suggest that genetic determinants of response to infliximab therapy exist in the HLA complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15077289
was generated by: ECO_0000203

NP55113.RAV9l-BQsDRhO4P07e IKgX9OvUrK-12yqA0vnX7EcgmE
has assertion: NP55113.RAV9l-BQsDRhO4P07e IKgX9OvUrK-12yqA0vnX7EcgmE130 assertion
has provenance: NP55113.RAV9l-BQsDRhO4P07e IKgX9OvUrK-12yqA0vnX7EcgmE130 provenance
has publication info: NP55113.RAV9l-BQsDRhO4P07e IKgX9OvUrK-12yqA0vnX7EcgmE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55113.RAV9l-BQsDRhO4P07e IKgX9OvUrK-12yqA0vnX7EcgmE130 assertion
type: Assertion
description: [Duration of non-Insulin-dependent diabetes mellitus and the TNF-beta NcoI genotype as predictive factors in proliferative diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11399938
was generated by: ECO_0000203

NP55122.RAWueM4Bo1A0vQInbZXvMQUHogwLG6vEN6fAUNEZRdb70
has assertion: NP55122.RAWueM4Bo1A0vQInbZXvMQUHogwLG6vEN6fAUNEZRdb70130 assertion
has provenance: NP55122.RAWueM4Bo1A0vQInbZXvMQUHogwLG6vEN6fAUNEZRdb70130 provenance
has publication info: NP55122.RAWueM4Bo1A0vQInbZXvMQUHogwLG6vEN6fAUNEZRdb70130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55122.RAWueM4Bo1A0vQInbZXvMQUHogwLG6vEN6fAUNEZRdb70130 assertion
type: Assertion
description: [Study on some susceptible genes of systemic lupus erythematosus in Han nationality of China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9275640
was generated by: ECO_0000203

NP55123.RAcVFfd559KlF9kE7rh-ijhgjEpXdt1A1tuot9GizvQ7Q
has assertion: NP55123.RAcVFfd559KlF9kE7rh-ijhgjEpXdt1A1tuot9GizvQ7Q130 assertion
has provenance: NP55123.RAcVFfd559KlF9kE7rh-ijhgjEpXdt1A1tuot9GizvQ7Q130 provenance
has publication info: NP55123.RAcVFfd559KlF9kE7rh-ijhgjEpXdt1A1tuot9GizvQ7Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55123.RAcVFfd559KlF9kE7rh-ijhgjEpXdt1A1tuot9GizvQ7Q130 assertion
type: Assertion
description: [We investigated the Nco I restriction fragment length polymorphism (RFLP) of the tumor necrosis factor beta (TNFB) gene in 173 patients with systemic lupus erythematosus (SLE), 192 unrelated healthy controls, and eleven panel families, all of German origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/8436420
was generated by: ECO_0000203

NP55124.RAYBdO3gj8GYkhjm5QPQZzLkxeWh7NdyUwVeKrh1X2x3w
has assertion: NP55124.RAYBdO3gj8GYkhjm5QPQZzLkxeWh7NdyUwVeKrh1X2x3w130 assertion
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has publication info: NP55124.RAYBdO3gj8GYkhjm5QPQZzLkxeWh7NdyUwVeKrh1X2x3w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55124.RAYBdO3gj8GYkhjm5QPQZzLkxeWh7NdyUwVeKrh1X2x3w130 assertion
type: Assertion
description: [High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19851445
was generated by: ECO_0000203

NP55127.RAWgRBi10APVqnFNPp6ZfxPsYb1wdLnUWettj6lJ9WCTs
has assertion: NP55127.RAWgRBi10APVqnFNPp6ZfxPsYb1wdLnUWettj6lJ9WCTs130 assertion
has provenance: NP55127.RAWgRBi10APVqnFNPp6ZfxPsYb1wdLnUWettj6lJ9WCTs130 provenance
has publication info: NP55127.RAWgRBi10APVqnFNPp6ZfxPsYb1wdLnUWettj6lJ9WCTs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55127.RAWgRBi10APVqnFNPp6ZfxPsYb1wdLnUWettj6lJ9WCTs130 assertion
type: Assertion
description: [Since these variants are implicated in the susceptibility and severity of several immunologic disorders, the results support the hypothesis that common genetic determinants influence shared mechanisms of autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20335604
was generated by: ECO_0000203

NP55131.RAdHF7-cD4rtrhJLsuFRCsNsvP0ng7XZ1k5ePknD15GU8
has assertion: NP55131.RAdHF7-cD4rtrhJLsuFRCsNsvP0ng7XZ1k5ePknD15GU8130 assertion
has provenance: NP55131.RAdHF7-cD4rtrhJLsuFRCsNsvP0ng7XZ1k5ePknD15GU8130 provenance
has publication info: NP55131.RAdHF7-cD4rtrhJLsuFRCsNsvP0ng7XZ1k5ePknD15GU8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55131.RAdHF7-cD4rtrhJLsuFRCsNsvP0ng7XZ1k5ePknD15GU8130 assertion
type: Assertion
description: [There was no association between the TNFB polymorphism and ARDS mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16135717
was generated by: ECO_0000203

NP55132.RAWTK 4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs
has assertion: NP55132.RAWTK 4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130 assertion
has provenance: NP55132.RAWTK 4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130 provenance
has publication info: NP55132.RAWTK 4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55132.RAWTK 4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130 assertion
type: Assertion
description: [Our data suggest an effect of the TNFalpha-308 polymorphism on the age at onset of late AD. This represents additional evidence of the importance of genetic variation at the proinflammatory components in the origin and progression of this common NEUROLOGICALenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12116197
was generated by: ECO_0000203

NP55133.RAfL2kS3fy2CC429bYTEan1p1DYtpSe7ay6j6aBLp6p7w
has assertion: NP55133.RAfL2kS3fy2CC429bYTEan1p1DYtpSe7ay6j6aBLp6p7w130 assertion
has provenance: NP55133.RAfL2kS3fy2CC429bYTEan1p1DYtpSe7ay6j6aBLp6p7w130 provenance
has publication info: NP55133.RAfL2kS3fy2CC429bYTEan1p1DYtpSe7ay6j6aBLp6p7w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55133.RAfL2kS3fy2CC429bYTEan1p1DYtpSe7ay6j6aBLp6p7w130 assertion
type: Assertion
description: [Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19141999
was generated by: ECO_0000203

NP55134.RAb0ZjqkG9mN4UAR2jIG4NE0oOMPF7KsZvzmJ2ys8dYVM
has assertion: NP55134.RAb0ZjqkG9mN4UAR2jIG4NE0oOMPF7KsZvzmJ2ys8dYVM130 assertion
has provenance: NP55134.RAb0ZjqkG9mN4UAR2jIG4NE0oOMPF7KsZvzmJ2ys8dYVM130 provenance
has publication info: NP55134.RAb0ZjqkG9mN4UAR2jIG4NE0oOMPF7KsZvzmJ2ys8dYVM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55134.RAb0ZjqkG9mN4UAR2jIG4NE0oOMPF7KsZvzmJ2ys8dYVM130 assertion
type: Assertion
description: [We investigated the association of polymorphisms in the tumor necrosis factor (TNF) microsatellite as well as the promoter region of the TNFA gene and the TNFB gene with palmoplantar pustulosis (PPP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12691703
was generated by: ECO_0000203

NP55137.RAd5-J7Cs8jRVzPcHNpVy8zz3TQaB3yIBNNRWnrI MaoI
has assertion: NP55137.RAd5-J7Cs8jRVzPcHNpVy8zz3TQaB3yIBNNRWnrI MaoI130 assertion
has provenance: NP55137.RAd5-J7Cs8jRVzPcHNpVy8zz3TQaB3yIBNNRWnrI MaoI130 provenance
has publication info: NP55137.RAd5-J7Cs8jRVzPcHNpVy8zz3TQaB3yIBNNRWnrI MaoI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55137.RAd5-J7Cs8jRVzPcHNpVy8zz3TQaB3yIBNNRWnrI MaoI130 assertion
type: Assertion
description: [To investigate the association between tumor necrosis factor-beta (TNF-beta) gene polymorphisms and coronary heart disease (CHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15583987
was generated by: ECO_0000203

NP55140.RAYvDjNnfxZrOHPYgWK1YC2NaVxD2Y Wc4Biamr4XodTI
has assertion: NP55140.RAYvDjNnfxZrOHPYgWK1YC2NaVxD2Y Wc4Biamr4XodTI130 assertion
has provenance: NP55140.RAYvDjNnfxZrOHPYgWK1YC2NaVxD2Y Wc4Biamr4XodTI130 provenance
has publication info: NP55140.RAYvDjNnfxZrOHPYgWK1YC2NaVxD2Y Wc4Biamr4XodTI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55140.RAYvDjNnfxZrOHPYgWK1YC2NaVxD2Y Wc4Biamr4XodTI130 assertion
type: Assertion
description: [A positive family history of psoriasis was associated with a higher B1 allele frequency in NcoI TNFbeta (P = 0.011).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11194890
was generated by: ECO_0000203

NP55143.RAZab6udX5AmmEOVsvBV-7nFzMxWVlY tE1DA-cK1d744
has assertion: NP55143.RAZab6udX5AmmEOVsvBV-7nFzMxWVlY tE1DA-cK1d744130 assertion
has provenance: NP55143.RAZab6udX5AmmEOVsvBV-7nFzMxWVlY tE1DA-cK1d744130 provenance
has publication info: NP55143.RAZab6udX5AmmEOVsvBV-7nFzMxWVlY tE1DA-cK1d744130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55143.RAZab6udX5AmmEOVsvBV-7nFzMxWVlY tE1DA-cK1d744130 assertion
type: Assertion
description: [Systemic lupus erythematosus with nephritis is strongly associated with the TNFB*2 homozygote in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9157084
was generated by: ECO_0000203

NP55150.RAdvVAhhyJPzie0oQeux7eG8vKl88uUW-uR-gCoo WaeQ
has assertion: NP55150.RAdvVAhhyJPzie0oQeux7eG8vKl88uUW-uR-gCoo WaeQ130 assertion
has provenance: NP55150.RAdvVAhhyJPzie0oQeux7eG8vKl88uUW-uR-gCoo WaeQ130 provenance
has publication info: NP55150.RAdvVAhhyJPzie0oQeux7eG8vKl88uUW-uR-gCoo WaeQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55150.RAdvVAhhyJPzie0oQeux7eG8vKl88uUW-uR-gCoo WaeQ130 assertion
type: Assertion
description: [We examined the association of seven single nucleotide polymorphisms (SNPs) across the LTA gene, and their related haplotypes, with risk of myocardial infarction (MI) in the International Study of Infarct Survival (ISIS) case-control study involving 6,928 non-fatal MI cases and 2,712 unrelated controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16839190
was generated by: ECO_0000203

NP55151.RAUGbYSAK3b4-ROPHO8Aa RVJq0eTURGVOL50BmKgJa6A
has assertion: NP55151.RAUGbYSAK3b4-ROPHO8Aa RVJq0eTURGVOL50BmKgJa6A130 assertion
has provenance: NP55151.RAUGbYSAK3b4-ROPHO8Aa RVJq0eTURGVOL50BmKgJa6A130 provenance
has publication info: NP55151.RAUGbYSAK3b4-ROPHO8Aa RVJq0eTURGVOL50BmKgJa6A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55151.RAUGbYSAK3b4-ROPHO8Aa RVJq0eTURGVOL50BmKgJa6A130 assertion
type: Assertion
description: [We have identified functional SNPs within the lymphotoxin-alpha gene located on chromosome 6p21 conferred susceptibility to MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17071996
was generated by: ECO_0000203

NP55154.RAdAxN3ZjdLjkOtPhUkm2Szwn IdAlT-7-cLcgvD1kWxI
has assertion: NP55154.RAdAxN3ZjdLjkOtPhUkm2Szwn IdAlT-7-cLcgvD1kWxI130 assertion
has provenance: NP55154.RAdAxN3ZjdLjkOtPhUkm2Szwn IdAlT-7-cLcgvD1kWxI130 provenance
has publication info: NP55154.RAdAxN3ZjdLjkOtPhUkm2Szwn IdAlT-7-cLcgvD1kWxI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55154.RAdAxN3ZjdLjkOtPhUkm2Szwn IdAlT-7-cLcgvD1kWxI130 assertion
type: Assertion
description: [Our data suggest that combined genotypes composed of the TNF-alpha and LT-alpha gene polymorphisms may influence the susceptibility to chronic periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12828656
was generated by: ECO_0000203

NP55159.RAR3xzIDWh7vyV4f-esGvA5hF7w0VWdYhfvcVAX5maJPw
has assertion: NP55159.RAR3xzIDWh7vyV4f-esGvA5hF7w0VWdYhfvcVAX5maJPw130 assertion
has provenance: NP55159.RAR3xzIDWh7vyV4f-esGvA5hF7w0VWdYhfvcVAX5maJPw130 provenance
has publication info: NP55159.RAR3xzIDWh7vyV4f-esGvA5hF7w0VWdYhfvcVAX5maJPw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55159.RAR3xzIDWh7vyV4f-esGvA5hF7w0VWdYhfvcVAX5maJPw130 assertion
type: Assertion
description: [Support Vector Machine based feature selection method in this research found novel association between combinations of SNPs and T2D in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20416077
was generated by: ECO_0000203

NP55164.RAfbkFuaiF2uf QgFtXuAuGlfijjIU3USOkr0w r GPnk
has assertion: NP55164.RAfbkFuaiF2uf QgFtXuAuGlfijjIU3USOkr0w r GPnk130 assertion
has provenance: NP55164.RAfbkFuaiF2uf QgFtXuAuGlfijjIU3USOkr0w r GPnk130 provenance
has publication info: NP55164.RAfbkFuaiF2uf QgFtXuAuGlfijjIU3USOkr0w r GPnk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55164.RAfbkFuaiF2uf QgFtXuAuGlfijjIU3USOkr0w r GPnk130 assertion
type: Assertion
description: [ Several reports have indicated that different HLA products and genes may be risk factors for or protective factors against the development of atopy. We report no association between polymorphisms in the LT-alpha and TAP-1 genes alone and atopic diseases in the central Europe Caucasian (Czech) population, but there was an interesting interaction between the TAP333 and LT-alpha polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11591192
was generated by: ECO_0000203

NP55166.RAZG cNcXozG3R2Utwnr9CttcDpira7EUOsSkg163upR8
has assertion: NP55166.RAZG cNcXozG3R2Utwnr9CttcDpira7EUOsSkg163upR8130 assertion
has provenance: NP55166.RAZG cNcXozG3R2Utwnr9CttcDpira7EUOsSkg163upR8130 provenance
has publication info: NP55166.RAZG cNcXozG3R2Utwnr9CttcDpira7EUOsSkg163upR8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55166.RAZG cNcXozG3R2Utwnr9CttcDpira7EUOsSkg163upR8130 assertion
type: Assertion
description: [Our study confirms that HLA class III region seems involved in familial predisposition to atopy, and C4B gene probably acts as a marker of a more restricted subregion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16788244
was generated by: ECO_0000203

NP55167.RAf GorMFwW917Rgi-iSODNtQcXCS4qsMoxjRsN7F73uM
has assertion: NP55167.RAf GorMFwW917Rgi-iSODNtQcXCS4qsMoxjRsN7F73uM130 assertion
has provenance: NP55167.RAf GorMFwW917Rgi-iSODNtQcXCS4qsMoxjRsN7F73uM130 provenance
has publication info: NP55167.RAf GorMFwW917Rgi-iSODNtQcXCS4qsMoxjRsN7F73uM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55167.RAf GorMFwW917Rgi-iSODNtQcXCS4qsMoxjRsN7F73uM130 assertion
type: Assertion
description: [We previously reported that the G2019S LRRK2 mutation-which is the most common LRRK2 mutation-was not found in a sample of 453 Korean PD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19513331
was generated by: ECO_0000203

NP55168.RAb2K6Jkp6cQIVeB4oxZPLw3cUdLtPYc-nJrjmrgRGmrk
has assertion: NP55168.RAb2K6Jkp6cQIVeB4oxZPLw3cUdLtPYc-nJrjmrgRGmrk130 assertion
has provenance: NP55168.RAb2K6Jkp6cQIVeB4oxZPLw3cUdLtPYc-nJrjmrgRGmrk130 provenance
has publication info: NP55168.RAb2K6Jkp6cQIVeB4oxZPLw3cUdLtPYc-nJrjmrgRGmrk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55168.RAb2K6Jkp6cQIVeB4oxZPLw3cUdLtPYc-nJrjmrgRGmrk130 assertion
type: Assertion
description: [Absence of commonly reported leucine-rich repeat kinase 2 mutations in Eastern Indian Parkinson's disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20722494
was generated by: ECO_0000203

NP55173.RAftRG-E0EK8ndyZzeuJ8rYZyiy2zt3V7pXmkEf55PST8
has assertion: NP55173.RAftRG-E0EK8ndyZzeuJ8rYZyiy2zt3V7pXmkEf55PST8130 assertion
has provenance: NP55173.RAftRG-E0EK8ndyZzeuJ8rYZyiy2zt3V7pXmkEf55PST8130 provenance
has publication info: NP55173.RAftRG-E0EK8ndyZzeuJ8rYZyiy2zt3V7pXmkEf55PST8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55173.RAftRG-E0EK8ndyZzeuJ8rYZyiy2zt3V7pXmkEf55PST8130 assertion
type: Assertion
description: [Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20182943
was generated by: ECO_0000203

NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw
has assertion: NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130 assertion
has provenance: NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130 provenance
has publication info: NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130 assertion
type: Assertion
description: [According to our data, the variation at the LRPAP1 gene is associated with the risk of developing LOAD. This is in agreement with the role of the LRPAP1 protein in the amyloidogenic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11425005
was generated by: ECO_0000203

NP55190.RAWZ1qsno0NRFI5MNxR E4WXRb8CoVPZ6yZBl-RQ0SzN0
has assertion: NP55190.RAWZ1qsno0NRFI5MNxR E4WXRb8CoVPZ6yZBl-RQ0SzN0130 assertion
has provenance: NP55190.RAWZ1qsno0NRFI5MNxR E4WXRb8CoVPZ6yZBl-RQ0SzN0130 provenance
has publication info: NP55190.RAWZ1qsno0NRFI5MNxR E4WXRb8CoVPZ6yZBl-RQ0SzN0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55190.RAWZ1qsno0NRFI5MNxR E4WXRb8CoVPZ6yZBl-RQ0SzN0130 assertion
type: Assertion
description: [ These data suggest that LRP6, VEGF, and VLDLR may play a role in the risk of developing AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16384981
was generated by: ECO_0000203

NP55193.RAYSsddDrp839tEvtjBfvOfoD-wS-7B92zSdx5 9N2 3k
has assertion: NP55193.RAYSsddDrp839tEvtjBfvOfoD-wS-7B92zSdx5 9N2 3k130 assertion
has provenance: NP55193.RAYSsddDrp839tEvtjBfvOfoD-wS-7B92zSdx5 9N2 3k130 provenance
has publication info: NP55193.RAYSsddDrp839tEvtjBfvOfoD-wS-7B92zSdx5 9N2 3k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55193.RAYSsddDrp839tEvtjBfvOfoD-wS-7B92zSdx5 9N2 3k130 assertion
type: Assertion
description: [Our objective was to investigate the role of the APOE coding region polymorphisms epsilon 2, epsilon 3, and epsilon 4 and APOE promoter variants A/T at position -491 and G/T at -219, as well as LRP polymorphism C/T, as risk factors for AD in Brazilian individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18317248
was generated by: ECO_0000203

NP55199.RAZg5PxBjm6MoaoydmpbQUl71H9uC6uI43vpRpDe41iOM
has assertion: NP55199.RAZg5PxBjm6MoaoydmpbQUl71H9uC6uI43vpRpDe41iOM130 assertion
has provenance: NP55199.RAZg5PxBjm6MoaoydmpbQUl71H9uC6uI43vpRpDe41iOM130 provenance
has publication info: NP55199.RAZg5PxBjm6MoaoydmpbQUl71H9uC6uI43vpRpDe41iOM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55199.RAZg5PxBjm6MoaoydmpbQUl71H9uC6uI43vpRpDe41iOM130 assertion
type: Assertion
description: [Lack of interaction between LRP1 and A2M polymorphisms for the risk of Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20637261
was generated by: ECO_0000203

NP55200.RAQ z-KLyQKwRzoMSmGGObutc37pKgwvkTqHcHEswo7is
has assertion: NP55200.RAQ z-KLyQKwRzoMSmGGObutc37pKgwvkTqHcHEswo7is130 assertion
has provenance: NP55200.RAQ z-KLyQKwRzoMSmGGObutc37pKgwvkTqHcHEswo7is130 provenance
has publication info: NP55200.RAQ z-KLyQKwRzoMSmGGObutc37pKgwvkTqHcHEswo7is130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55200.RAQ z-KLyQKwRzoMSmGGObutc37pKgwvkTqHcHEswo7is130 assertion
type: Assertion
description: [Genetic interaction between tau and the apolipoprotein E receptor LRP1 Increases Alzheimer's disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19684401
was generated by: ECO_0000203

NP55202.RAfWl uxpqalBrYWQfwiT0vcwaBlUTJXsNAM2she4VPeY
has assertion: NP55202.RAfWl uxpqalBrYWQfwiT0vcwaBlUTJXsNAM2she4VPeY130 assertion
has provenance: NP55202.RAfWl uxpqalBrYWQfwiT0vcwaBlUTJXsNAM2she4VPeY130 provenance
has publication info: NP55202.RAfWl uxpqalBrYWQfwiT0vcwaBlUTJXsNAM2she4VPeY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55202.RAfWl uxpqalBrYWQfwiT0vcwaBlUTJXsNAM2she4VPeY130 assertion
type: Assertion
description: [We genotyped 210 patients with early MI (<55 years) and 200 healthy control participants for three polymorphisms in the LRP, LRPAP and alpha2 M genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12394648
was generated by: ECO_0000203

NP55204.RAbF-yfk-6Mya5PML84zfThRqU7Er jig09Yq5bRQTs90
has assertion: NP55204.RAbF-yfk-6Mya5PML84zfThRqU7Er jig09Yq5bRQTs90130 assertion
has provenance: NP55204.RAbF-yfk-6Mya5PML84zfThRqU7Er jig09Yq5bRQTs90130 provenance
has publication info: NP55204.RAbF-yfk-6Mya5PML84zfThRqU7Er jig09Yq5bRQTs90130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55204.RAbF-yfk-6Mya5PML84zfThRqU7Er jig09Yq5bRQTs90130 assertion
type: Assertion
description: [We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19948975
was generated by: ECO_0000203

NP55206.RAQsoV7ZgPY1GGggheYdHYJy4KzlsuZfhvH7z0xzG6Tr8
has assertion: NP55206.RAQsoV7ZgPY1GGggheYdHYJy4KzlsuZfhvH7z0xzG6Tr8130 assertion
has provenance: NP55206.RAQsoV7ZgPY1GGggheYdHYJy4KzlsuZfhvH7z0xzG6Tr8130 provenance
has publication info: NP55206.RAQsoV7ZgPY1GGggheYdHYJy4KzlsuZfhvH7z0xzG6Tr8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55206.RAQsoV7ZgPY1GGggheYdHYJy4KzlsuZfhvH7z0xzG6Tr8130 assertion
type: Assertion
description: [ The T allele of the C766T polymorphism in the LRP1 gene is associated with an increased risk of breast cancer development in women of Caucasian origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12793904
was generated by: ECO_0000203

NP55208.RASSTOuWmdFEM6ki9dcWQsE7TU8t4 q6iKRpxQVTh KBY
has assertion: NP55208.RASSTOuWmdFEM6ki9dcWQsE7TU8t4 q6iKRpxQVTh KBY130 assertion
has provenance: NP55208.RASSTOuWmdFEM6ki9dcWQsE7TU8t4 q6iKRpxQVTh KBY130 provenance
has publication info: NP55208.RASSTOuWmdFEM6ki9dcWQsE7TU8t4 q6iKRpxQVTh KBY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55208.RASSTOuWmdFEM6ki9dcWQsE7TU8t4 q6iKRpxQVTh KBY130 assertion
type: Assertion
description: [Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12082592
was generated by: ECO_0000203

NP55213.RATc0QkgfAHQbUFHhgxG76vw QX5WrTfcHM7X98P743ZQ
has assertion: NP55213.RATc0QkgfAHQbUFHhgxG76vw QX5WrTfcHM7X98P743ZQ130 assertion
has provenance: NP55213.RATc0QkgfAHQbUFHhgxG76vw QX5WrTfcHM7X98P743ZQ130 provenance
has publication info: NP55213.RATc0QkgfAHQbUFHhgxG76vw QX5WrTfcHM7X98P743ZQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55213.RATc0QkgfAHQbUFHhgxG76vw QX5WrTfcHM7X98P743ZQ130 assertion
type: Assertion
description: [The S447X polymorphism of the lipoprotein lipase gene is associated with lipoprotein lipid and blood pressure levels in Chinese patients with essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15257172
was generated by: ECO_0000203

NP55221.RAan3aFl6nS52z6VXY4ZGD o 22ePwfuHwBDZ4goUaHlQ
has assertion: NP55221.RAan3aFl6nS52z6VXY4ZGD o 22ePwfuHwBDZ4goUaHlQ130 assertion
has provenance: NP55221.RAan3aFl6nS52z6VXY4ZGD o 22ePwfuHwBDZ4goUaHlQ130 provenance
has publication info: NP55221.RAan3aFl6nS52z6VXY4ZGD o 22ePwfuHwBDZ4goUaHlQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55221.RAan3aFl6nS52z6VXY4ZGD o 22ePwfuHwBDZ4goUaHlQ130 assertion
type: Assertion
description: [A cohort of 1002 heterozygous FH patients was genotyped for polymorphisms in the genes encoding for ATP-binding cassette transporter A1, apolipoprotein (apo) AIV, apoCIII, apoE, cholesteryl transfer ester protein, hepatic lipase, lipoprotein lipase, and two paraoxonases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16030523
was generated by: ECO_0000203

NP55222.RAQsFUyROpXZh0850i5RONiYg n x6KKaM3sVWokZ M1Q
has assertion: NP55222.RAQsFUyROpXZh0850i5RONiYg n x6KKaM3sVWokZ M1Q130 assertion
has provenance: NP55222.RAQsFUyROpXZh0850i5RONiYg n x6KKaM3sVWokZ M1Q130 provenance
has publication info: NP55222.RAQsFUyROpXZh0850i5RONiYg n x6KKaM3sVWokZ M1Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55222.RAQsFUyROpXZh0850i5RONiYg n x6KKaM3sVWokZ M1Q130 assertion
type: Assertion
description: [Our results indicated a strong association of sequence variants of HMGCR, SREBF1 and ABCG8 genes with the reduction of LDL-C after statin treatment in a Chinese population. Future studies on the genes of drug-metabolism enzymes and transporters are warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20235787
was generated by: ECO_0000203

NP55224.RAfg4EZQri9OivCCoSgNFnKj-bL5Qxo1QcesjpDkCiSdU
has assertion: NP55224.RAfg4EZQri9OivCCoSgNFnKj-bL5Qxo1QcesjpDkCiSdU130 assertion
has provenance: NP55224.RAfg4EZQri9OivCCoSgNFnKj-bL5Qxo1QcesjpDkCiSdU130 provenance
has publication info: NP55224.RAfg4EZQri9OivCCoSgNFnKj-bL5Qxo1QcesjpDkCiSdU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55224.RAfg4EZQri9OivCCoSgNFnKj-bL5Qxo1QcesjpDkCiSdU130 assertion
type: Assertion
description: [PPARgamma and LPL have intractable roles in pathways that lead to CAD, but their gene polymorphisms associate differently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20430250
was generated by: ECO_0000203

NP55225.RAX0MFJO9QavyqdpiexN2VXbxN3iKZu9ZmSRFkNjMSi3A
has assertion: NP55225.RAX0MFJO9QavyqdpiexN2VXbxN3iKZu9ZmSRFkNjMSi3A130 assertion
has provenance: NP55225.RAX0MFJO9QavyqdpiexN2VXbxN3iKZu9ZmSRFkNjMSi3A130 provenance
has publication info: NP55225.RAX0MFJO9QavyqdpiexN2VXbxN3iKZu9ZmSRFkNjMSi3A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55225.RAX0MFJO9QavyqdpiexN2VXbxN3iKZu9ZmSRFkNjMSi3A130 assertion
type: Assertion
description: [The presence of the S447X lipoprotein lipase polymorphism was not associated with the incidence of CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17533471
was generated by: ECO_0000203

NP55228.RASQ9dchdD0ZBSC1lORcfld6o U5Xb1WmU4Sgouyq77sI
has assertion: NP55228.RASQ9dchdD0ZBSC1lORcfld6o U5Xb1WmU4Sgouyq77sI130 assertion
has provenance: NP55228.RASQ9dchdD0ZBSC1lORcfld6o U5Xb1WmU4Sgouyq77sI130 provenance
has publication info: NP55228.RASQ9dchdD0ZBSC1lORcfld6o U5Xb1WmU4Sgouyq77sI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55228.RASQ9dchdD0ZBSC1lORcfld6o U5Xb1WmU4Sgouyq77sI130 assertion
type: Assertion
description: [Hence, we examined the influence of the -93T/G, D9N, N291S, and S447X polymorphisms in the lipoprotein lipase (LPL) gene on CAD risk and lipid levels in Croatian patients with and without angiographically confirmed CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12747600
was generated by: ECO_0000203

NP55233.RAaxsNH4OCZq4-bf I1jSZJZF57n341W51Wm0hIj4a184
has assertion: NP55233.RAaxsNH4OCZq4-bf I1jSZJZF57n341W51Wm0hIj4a184130 assertion
has provenance: NP55233.RAaxsNH4OCZq4-bf I1jSZJZF57n341W51Wm0hIj4a184130 provenance
has publication info: NP55233.RAaxsNH4OCZq4-bf I1jSZJZF57n341W51Wm0hIj4a184130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55233.RAaxsNH4OCZq4-bf I1jSZJZF57n341W51Wm0hIj4a184130 assertion
type: Assertion
description: [We identified a cluster of polymorphisms in APOE, SOAT1, APOE 5'-untranslated region, OLR1, CYP46A1, LPL, LIPA, and APOA4 conferring significant (p = .0002) susceptibility for Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16013913
was generated by: ECO_0000203

NP55239.RAb8rfk-TDNDZ2O93LYEYlJ6-Cx81R-GwcCmIlBazwroY
has assertion: NP55239.RAb8rfk-TDNDZ2O93LYEYlJ6-Cx81R-GwcCmIlBazwroY130 assertion
has provenance: NP55239.RAb8rfk-TDNDZ2O93LYEYlJ6-Cx81R-GwcCmIlBazwroY130 provenance
has publication info: NP55239.RAb8rfk-TDNDZ2O93LYEYlJ6-Cx81R-GwcCmIlBazwroY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55239.RAb8rfk-TDNDZ2O93LYEYlJ6-Cx81R-GwcCmIlBazwroY130 assertion
type: Assertion
description: [Lipoprotein lipase 1595 c/g and hepatic lipase -480 c/t polymorphisms--impact on lipid profile in incident dialysis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19052449
was generated by: ECO_0000203

NP55242.RAarzaRaTx7Xb-dKr7 -kK5VacB lhKvyJf zoEHH-ulw
has assertion: NP55242.RAarzaRaTx7Xb-dKr7 -kK5VacB lhKvyJf zoEHH-ulw130 assertion
has provenance: NP55242.RAarzaRaTx7Xb-dKr7 -kK5VacB lhKvyJf zoEHH-ulw130 provenance
has publication info: NP55242.RAarzaRaTx7Xb-dKr7 -kK5VacB lhKvyJf zoEHH-ulw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55242.RAarzaRaTx7Xb-dKr7 -kK5VacB lhKvyJf zoEHH-ulw130 assertion
type: Assertion
description: [For a modest panel of selected genotypes, CHD-risk estimates incorporating CRFs and genotype-risk factor interactions were more effective than risk estimates that used CRFs alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17130180
was generated by: ECO_0000203

NP55243.RAfXQWJCAr-CZASqMRGL7LRdqeMiE1oHQ7fdcguYF0mEo
has assertion: NP55243.RAfXQWJCAr-CZASqMRGL7LRdqeMiE1oHQ7fdcguYF0mEo130 assertion
has provenance: NP55243.RAfXQWJCAr-CZASqMRGL7LRdqeMiE1oHQ7fdcguYF0mEo130 provenance
has publication info: NP55243.RAfXQWJCAr-CZASqMRGL7LRdqeMiE1oHQ7fdcguYF0mEo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55243.RAfXQWJCAr-CZASqMRGL7LRdqeMiE1oHQ7fdcguYF0mEo130 assertion
type: Assertion
description: [Results from the current study suggest that interaction effects between alcohol consumption and HDL cholesterol metabolism gene variation influence the risk of incident CHD in black men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17568951
was generated by: ECO_0000203

NP55244.RAfbSvRWf3ZhU -SZUK5KEXdNTuA5k0pTjQMvIVfG56Rg
has assertion: NP55244.RAfbSvRWf3ZhU -SZUK5KEXdNTuA5k0pTjQMvIVfG56Rg130 assertion
has provenance: NP55244.RAfbSvRWf3ZhU -SZUK5KEXdNTuA5k0pTjQMvIVfG56Rg130 provenance
has publication info: NP55244.RAfbSvRWf3ZhU -SZUK5KEXdNTuA5k0pTjQMvIVfG56Rg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55244.RAfbSvRWf3ZhU -SZUK5KEXdNTuA5k0pTjQMvIVfG56Rg130 assertion
type: Assertion
description: [Effect of gender on phenotypic expression of the S447X mutation in LPL: the Copenhagen City Heart Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12208477
was generated by: ECO_0000203

NP55245.RATLcElCUlKDd7pr50h09GY5SBhlr1r5tg2ZFguQFflKQ
has assertion: NP55245.RATLcElCUlKDd7pr50h09GY5SBhlr1r5tg2ZFguQFflKQ130 assertion
has provenance: NP55245.RATLcElCUlKDd7pr50h09GY5SBhlr1r5tg2ZFguQFflKQ130 provenance
has publication info: NP55245.RATLcElCUlKDd7pr50h09GY5SBhlr1r5tg2ZFguQFflKQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55245.RATLcElCUlKDd7pr50h09GY5SBhlr1r5tg2ZFguQFflKQ130 assertion
type: Assertion
description: [Genetic variants in lipoprotein lipase may affect triglycerides, high-density lipoprotein (HDL), and risk of ischemic heart disease (IHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16418216
was generated by: ECO_0000203

NP55250.RAaD2gw0aZsUC9FXfXtegW 3mAueravdZUNtWGNu8lqYo
has assertion: NP55250.RAaD2gw0aZsUC9FXfXtegW 3mAueravdZUNtWGNu8lqYo130 assertion
has provenance: NP55250.RAaD2gw0aZsUC9FXfXtegW 3mAueravdZUNtWGNu8lqYo130 provenance
has publication info: NP55250.RAaD2gw0aZsUC9FXfXtegW 3mAueravdZUNtWGNu8lqYo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55250.RAaD2gw0aZsUC9FXfXtegW 3mAueravdZUNtWGNu8lqYo130 assertion
type: Assertion
description: [Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9678774
was generated by: ECO_0000203

NP55251.RARwTW4SZ5vi uqrKbr9Ge9lzGE4n 5zqhTjjpIp0Htyw
has assertion: NP55251.RARwTW4SZ5vi uqrKbr9Ge9lzGE4n 5zqhTjjpIp0Htyw130 assertion
has provenance: NP55251.RARwTW4SZ5vi uqrKbr9Ge9lzGE4n 5zqhTjjpIp0Htyw130 provenance
has publication info: NP55251.RARwTW4SZ5vi uqrKbr9Ge9lzGE4n 5zqhTjjpIp0Htyw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55251.RARwTW4SZ5vi uqrKbr9Ge9lzGE4n 5zqhTjjpIp0Htyw130 assertion
type: Assertion
description: [An intronic single nucleotide polymorphism in ABCA1 and the APOE epsilon3 allele are associated with reduced LDLc lowering by statins and identify individuals who may be resistant to maximal LDLc lowering by statins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20031551
was generated by: ECO_0000203

NP55254.RAU93NaJZo-ahptGjOVofd4b3KX5JJ0jmPgcH73Jh4-E4
has assertion: NP55254.RAU93NaJZo-ahptGjOVofd4b3KX5JJ0jmPgcH73Jh4-E4130 assertion
has provenance: NP55254.RAU93NaJZo-ahptGjOVofd4b3KX5JJ0jmPgcH73Jh4-E4130 provenance
has publication info: NP55254.RAU93NaJZo-ahptGjOVofd4b3KX5JJ0jmPgcH73Jh4-E4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55254.RAU93NaJZo-ahptGjOVofd4b3KX5JJ0jmPgcH73Jh4-E4130 assertion
type: Assertion
description: [Association of lipoprotein lipase (LPL) single nucleotide polymorphisms with type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18985010
was generated by: ECO_0000203

NP55258.RAVxbqYhujKuxN ZvRFVjPwZW8UAm74I UV5Xz51nr96k
has assertion: NP55258.RAVxbqYhujKuxN ZvRFVjPwZW8UAm74I UV5Xz51nr96k130 assertion
has provenance: NP55258.RAVxbqYhujKuxN ZvRFVjPwZW8UAm74I UV5Xz51nr96k130 provenance
has publication info: NP55258.RAVxbqYhujKuxN ZvRFVjPwZW8UAm74I UV5Xz51nr96k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55258.RAVxbqYhujKuxN ZvRFVjPwZW8UAm74I UV5Xz51nr96k130 assertion
type: Assertion
description: [Adding SNPs previously associated with fasting glucose, insulin, lipids or obesity to a genetic risk score for type 2 diabetes significantly increases the power to discriminate between people with and without clinically manifest type 2 diabetes compared with a model including only conventional type 2 diabetes loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20571754
was generated by: ECO_0000203

NP55259.RAZtftJR0g-mvTbIy-CIXom3nUG2m-ly9E-pVIozQ1V74
has assertion: NP55259.RAZtftJR0g-mvTbIy-CIXom3nUG2m-ly9E-pVIozQ1V74130 assertion
has provenance: NP55259.RAZtftJR0g-mvTbIy-CIXom3nUG2m-ly9E-pVIozQ1V74130 provenance
has publication info: NP55259.RAZtftJR0g-mvTbIy-CIXom3nUG2m-ly9E-pVIozQ1V74130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55259.RAZtftJR0g-mvTbIy-CIXom3nUG2m-ly9E-pVIozQ1V74130 assertion
type: Assertion
description: [The independent risk conferred by genetic variants encoding pathways such as inflammation and lipid metabolism, not adequately reflected by conventional biomarkers, may identify high-risk individuals for intensified control of modifiable risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20536507
was generated by: ECO_0000203

NP55263.RAbXi-DpizZkk4hjkbmVUYEnoC40Flvloy9OWi1f4a6EM
has assertion: NP55263.RAbXi-DpizZkk4hjkbmVUYEnoC40Flvloy9OWi1f4a6EM130 assertion
has provenance: NP55263.RAbXi-DpizZkk4hjkbmVUYEnoC40Flvloy9OWi1f4a6EM130 provenance
has publication info: NP55263.RAbXi-DpizZkk4hjkbmVUYEnoC40Flvloy9OWi1f4a6EM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55263.RAbXi-DpizZkk4hjkbmVUYEnoC40Flvloy9OWi1f4a6EM130 assertion
type: Assertion
description: [on the genetic causes of lipase activities outside of the normal range should be drawn with caution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19367320
was generated by: ECO_0000203

NP55270.RAVFapFlkbIxcAFmVsj Gqyq81NQCzOB4kEVtwcDTU9tU
has assertion: NP55270.RAVFapFlkbIxcAFmVsj Gqyq81NQCzOB4kEVtwcDTU9tU130 assertion
has provenance: NP55270.RAVFapFlkbIxcAFmVsj Gqyq81NQCzOB4kEVtwcDTU9tU130 provenance
has publication info: NP55270.RAVFapFlkbIxcAFmVsj Gqyq81NQCzOB4kEVtwcDTU9tU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55270.RAVFapFlkbIxcAFmVsj Gqyq81NQCzOB4kEVtwcDTU9tU130 assertion
type: Assertion
description: [Association of lipase lipoprotein polymorphisms with myocardial infarction and lipid levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17484619
was generated by: ECO_0000203

NP55273.RAT94ujOfVgeinZ078bxYHbSOjMLAPynS7UAaFrVGEogI
has assertion: NP55273.RAT94ujOfVgeinZ078bxYHbSOjMLAPynS7UAaFrVGEogI130 assertion
has provenance: NP55273.RAT94ujOfVgeinZ078bxYHbSOjMLAPynS7UAaFrVGEogI130 provenance
has publication info: NP55273.RAT94ujOfVgeinZ078bxYHbSOjMLAPynS7UAaFrVGEogI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55273.RAT94ujOfVgeinZ078bxYHbSOjMLAPynS7UAaFrVGEogI130 assertion
type: Assertion
description: [We conclude that carriers of N291S or combined D9N/ - 93T --> G mutations in the LPL gene are at substantially increased risk of pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10636447
was generated by: ECO_0000203

NP55275.RAZWmuYv-qBQQHGnNt9QvvXLofWNnRb0-L8gweooNQWhA
has assertion: NP55275.RAZWmuYv-qBQQHGnNt9QvvXLofWNnRb0-L8gweooNQWhA130 assertion
has provenance: NP55275.RAZWmuYv-qBQQHGnNt9QvvXLofWNnRb0-L8gweooNQWhA130 provenance
has publication info: NP55275.RAZWmuYv-qBQQHGnNt9QvvXLofWNnRb0-L8gweooNQWhA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55275.RAZWmuYv-qBQQHGnNt9QvvXLofWNnRb0-L8gweooNQWhA130 assertion
type: Assertion
description: [Lipoprotein lipase gene mutations and the risk of cardiovascular diseases in children with obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20350420
was generated by: ECO_0000203

NP55279.RAc5OxymmVG2HNP4lQ6c9bZNu08NYNId6vJeiI9ymShIg
has assertion: NP55279.RAc5OxymmVG2HNP4lQ6c9bZNu08NYNId6vJeiI9ymShIg130 assertion
has provenance: NP55279.RAc5OxymmVG2HNP4lQ6c9bZNu08NYNId6vJeiI9ymShIg130 provenance
has publication info: NP55279.RAc5OxymmVG2HNP4lQ6c9bZNu08NYNId6vJeiI9ymShIg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55279.RAc5OxymmVG2HNP4lQ6c9bZNu08NYNId6vJeiI9ymShIg130 assertion
type: Assertion
description: [To investigate the impact of lipoprotein lipase (LPL) gene S447X polymorphism on the relation between central obesity and lipid levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16552397
was generated by: ECO_0000203

NP55281.RAYw6p1tBBzB85yulJGOwy3y7Rgw600e18Lo9BOHPMmJ0
has assertion: NP55281.RAYw6p1tBBzB85yulJGOwy3y7Rgw600e18Lo9BOHPMmJ0130 assertion
has provenance: NP55281.RAYw6p1tBBzB85yulJGOwy3y7Rgw600e18Lo9BOHPMmJ0130 provenance
has publication info: NP55281.RAYw6p1tBBzB85yulJGOwy3y7Rgw600e18Lo9BOHPMmJ0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55281.RAYw6p1tBBzB85yulJGOwy3y7Rgw600e18Lo9BOHPMmJ0130 assertion
type: Assertion
description: [The aim of the present study was to examine the impact of the defective D9N and the null P207L mutations in the lipoprotein lipase (LPL) gene on high density lipoprotein (HDL) particle size in relation to specific environmental factors such as obesity, gender and menopausal status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11996946
was generated by: ECO_0000203

NP55286.RAbMkiFqea3W6 zAIl0ljmisBLBmeHGwwoFhf4oOJZbAY
has assertion: NP55286.RAbMkiFqea3W6 zAIl0ljmisBLBmeHGwwoFhf4oOJZbAY130 assertion
has provenance: NP55286.RAbMkiFqea3W6 zAIl0ljmisBLBmeHGwwoFhf4oOJZbAY130 provenance
has publication info: NP55286.RAbMkiFqea3W6 zAIl0ljmisBLBmeHGwwoFhf4oOJZbAY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55286.RAbMkiFqea3W6 zAIl0ljmisBLBmeHGwwoFhf4oOJZbAY130 assertion
type: Assertion
description: [Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19336475
was generated by: ECO_0000203

NP55288.RATlThoqURWH4MuoNLc9kHgCRsRnTSiPocgLyOHC3BfQA
has assertion: NP55288.RATlThoqURWH4MuoNLc9kHgCRsRnTSiPocgLyOHC3BfQA130 assertion
has provenance: NP55288.RATlThoqURWH4MuoNLc9kHgCRsRnTSiPocgLyOHC3BfQA130 provenance
has publication info: NP55288.RATlThoqURWH4MuoNLc9kHgCRsRnTSiPocgLyOHC3BfQA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55288.RATlThoqURWH4MuoNLc9kHgCRsRnTSiPocgLyOHC3BfQA130 assertion
type: Assertion
description: [Allele and genotype frequency distributions differed between Cases and Controls. Lp(a) concentrations differed according to PNR genotypes]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12127051
was generated by: ECO_0000203

NP55296.RAbLuE5P1QOju3N09N1FPimqtDcJ91jI7u-WsTn4C3yxk
has assertion: NP55296.RAbLuE5P1QOju3N09N1FPimqtDcJ91jI7u-WsTn4C3yxk130 assertion
has provenance: NP55296.RAbLuE5P1QOju3N09N1FPimqtDcJ91jI7u-WsTn4C3yxk130 provenance
has publication info: NP55296.RAbLuE5P1QOju3N09N1FPimqtDcJ91jI7u-WsTn4C3yxk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55296.RAbLuE5P1QOju3N09N1FPimqtDcJ91jI7u-WsTn4C3yxk130 assertion
type: Assertion
description: [Recently, a unique homozygous mutation in LMNA, which encodes lamin A/C, a component of the nuclear envelope, was identified in members of three Algerian families with ARCMT2 linked to chromosome 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14607793
was generated by: ECO_0000203

NP55298.RAWRR0 woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA
has assertion: NP55298.RAWRR0 woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130 assertion
has provenance: NP55298.RAWRR0 woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130 provenance
has publication info: NP55298.RAWRR0 woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55298.RAWRR0 woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130 assertion
type: Assertion
description: [These findings indicate that approximately half of the variance in mean s.c. abd. AS can be attributed to familial factors and that genetic variation in LMNA might not only underlie rare cases of FPLD, but may also contribute to variation in adipocyte size in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11243729
was generated by: ECO_0000203

NP55303.RAeAqsfTfX71BORys8n0PbzKyxaer2S75Xdxl0Mxb-RmQ
has assertion: NP55303.RAeAqsfTfX71BORys8n0PbzKyxaer2S75Xdxl0Mxb-RmQ130 assertion
has provenance: NP55303.RAeAqsfTfX71BORys8n0PbzKyxaer2S75Xdxl0Mxb-RmQ130 provenance
has publication info: NP55303.RAeAqsfTfX71BORys8n0PbzKyxaer2S75Xdxl0Mxb-RmQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55303.RAeAqsfTfX71BORys8n0PbzKyxaer2S75Xdxl0Mxb-RmQ130 assertion
type: Assertion
description: [ MBL deficiency is not a risk factor for SLE in women from the Canary Islands, but it is associated with lower prevalence of autoantibodies and with later age at disease onset and at SLE diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12672193
was generated by: ECO_0000203

NP55306.RAXdu0lutIaghLETglv5FrmMKOfHBrPZ4GRsJyvJvEv2o
has assertion: NP55306.RAXdu0lutIaghLETglv5FrmMKOfHBrPZ4GRsJyvJvEv2o130 assertion
has provenance: NP55306.RAXdu0lutIaghLETglv5FrmMKOfHBrPZ4GRsJyvJvEv2o130 provenance
has publication info: NP55306.RAXdu0lutIaghLETglv5FrmMKOfHBrPZ4GRsJyvJvEv2o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55306.RAXdu0lutIaghLETglv5FrmMKOfHBrPZ4GRsJyvJvEv2o130 assertion
type: Assertion
description: [This study confirms a role for HSL in glucose homeostasis and the reduced frequency of the low expressing -60G promoter variant in obese individuals, together with existing published data, suggests that this allele might be protective against obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15871848
was generated by: ECO_0000203

NP55307.RAW8wbZm6n63HKN8LBlR75eyFjUUo7naRe7ZCE7yBhuP4
has assertion: NP55307.RAW8wbZm6n63HKN8LBlR75eyFjUUo7naRe7ZCE7yBhuP4130 assertion
has provenance: NP55307.RAW8wbZm6n63HKN8LBlR75eyFjUUo7naRe7ZCE7yBhuP4130 provenance
has publication info: NP55307.RAW8wbZm6n63HKN8LBlR75eyFjUUo7naRe7ZCE7yBhuP4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:25+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55307.RAW8wbZm6n63HKN8LBlR75eyFjUUo7naRe7ZCE7yBhuP4130 assertion
type: Assertion
description: [ HSLi6 A5 homozygosity is a risk factor for body fat accumulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12534454
was generated by: ECO_0000203

NP55316.RAXDeyw9htmg8CAdFJkLHPsiktKptOVKxMijXKbNekXe4
has assertion: NP55316.RAXDeyw9htmg8CAdFJkLHPsiktKptOVKxMijXKbNekXe4130 assertion
has provenance: NP55316.RAXDeyw9htmg8CAdFJkLHPsiktKptOVKxMijXKbNekXe4130 provenance
has publication info: NP55316.RAXDeyw9htmg8CAdFJkLHPsiktKptOVKxMijXKbNekXe4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55316.RAXDeyw9htmg8CAdFJkLHPsiktKptOVKxMijXKbNekXe4130 assertion
type: Assertion
description: [Pharmacogenetic study of apolipoprotein E, cholesteryl ester transfer protein and hepatic lipase genes and simvastatin therapy in Brazilian subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16038892
was generated by: ECO_0000203

NP55317.RAU XrJfdHZK4J6IFXdHzqnnP-X-68up00h4MKxRbMqYg
has assertion: NP55317.RAU XrJfdHZK4J6IFXdHzqnnP-X-68up00h4MKxRbMqYg130 assertion
has provenance: NP55317.RAU XrJfdHZK4J6IFXdHzqnnP-X-68up00h4MKxRbMqYg130 provenance
has publication info: NP55317.RAU XrJfdHZK4J6IFXdHzqnnP-X-68up00h4MKxRbMqYg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55317.RAU XrJfdHZK4J6IFXdHzqnnP-X-68up00h4MKxRbMqYg130 assertion
type: Assertion
description: [The -514C/T polymorphism of the hepatic lipase gene significantly modulates the HDL-cholesterol response to statin treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16115483
was generated by: ECO_0000203

NP55321.RAcBfAjOHwqOh8ytlkpEiMhhsByDZ6zzyNrOrt9tTn06Q
has assertion: NP55321.RAcBfAjOHwqOh8ytlkpEiMhhsByDZ6zzyNrOrt9tTn06Q130 assertion
has provenance: NP55321.RAcBfAjOHwqOh8ytlkpEiMhhsByDZ6zzyNrOrt9tTn06Q130 provenance
has publication info: NP55321.RAcBfAjOHwqOh8ytlkpEiMhhsByDZ6zzyNrOrt9tTn06Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55321.RAcBfAjOHwqOh8ytlkpEiMhhsByDZ6zzyNrOrt9tTn06Q130 assertion
type: Assertion
description: [The Intermountain Healthcares Coronary Genetics study demonstrates the ability of a multigenic, multipathway GRS to improve discrimination of angiographic CAD. Genetic risk scores promise to increase understanding of the genetic basis of CAD and improve identification of individuals at increased CAD risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20691829
was generated by: ECO_0000203

NP55325.RAVrETm4Nx59IHABMwtsNJI0z cUN2iLkENN7lfKzq2FE
has assertion: NP55325.RAVrETm4Nx59IHABMwtsNJI0z cUN2iLkENN7lfKzq2FE130 assertion
has provenance: NP55325.RAVrETm4Nx59IHABMwtsNJI0z cUN2iLkENN7lfKzq2FE130 provenance
has publication info: NP55325.RAVrETm4Nx59IHABMwtsNJI0z cUN2iLkENN7lfKzq2FE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55325.RAVrETm4Nx59IHABMwtsNJI0z cUN2iLkENN7lfKzq2FE130 assertion
type: Assertion
description: [Family-based association studies of lipid gene polymorphisms in coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15979432
was generated by: ECO_0000203

NP55326.RAfeD2hoRhvaUc71SIb9aRAzG0W36CmVmh3MDbUsqWPT0
has assertion: NP55326.RAfeD2hoRhvaUc71SIb9aRAzG0W36CmVmh3MDbUsqWPT0130 assertion
has provenance: NP55326.RAfeD2hoRhvaUc71SIb9aRAzG0W36CmVmh3MDbUsqWPT0130 provenance
has publication info: NP55326.RAfeD2hoRhvaUc71SIb9aRAzG0W36CmVmh3MDbUsqWPT0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55326.RAfeD2hoRhvaUc71SIb9aRAzG0W36CmVmh3MDbUsqWPT0130 assertion
type: Assertion
description: [High HDL cholesterol does not protect against coronary artery disease when associated with combined cholesteryl ester transfer protein and hepatic lipase gene variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18164013
was generated by: ECO_0000203

NP55327.RATdXaAjrvLQOjAuXvgFcWSmeSBfnBLY9c8WwcOcN8IBs
has assertion: NP55327.RATdXaAjrvLQOjAuXvgFcWSmeSBfnBLY9c8WwcOcN8IBs130 assertion
has provenance: NP55327.RATdXaAjrvLQOjAuXvgFcWSmeSBfnBLY9c8WwcOcN8IBs130 provenance
has publication info: NP55327.RATdXaAjrvLQOjAuXvgFcWSmeSBfnBLY9c8WwcOcN8IBs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55327.RATdXaAjrvLQOjAuXvgFcWSmeSBfnBLY9c8WwcOcN8IBs130 assertion
type: Assertion
description: [Genetic study of common variants at the Apo E, Apo AI, Apo CIII, Apo B, lipoprotein lipase (LPL) and hepatic lipase (LIPC) genes and coronary artery disease (CAD): variation in LIPC gene associates with clinical outcomes in patients with established CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12964943
was generated by: ECO_0000203

NP55332.RAc-xrjI8ebwG7uSK1F2vf0N4O2XY4BWjmwr HOeFH3ZA
has assertion: NP55332.RAc-xrjI8ebwG7uSK1F2vf0N4O2XY4BWjmwr HOeFH3ZA130 assertion
has provenance: NP55332.RAc-xrjI8ebwG7uSK1F2vf0N4O2XY4BWjmwr HOeFH3ZA130 provenance
has publication info: NP55332.RAc-xrjI8ebwG7uSK1F2vf0N4O2XY4BWjmwr HOeFH3ZA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55332.RAc-xrjI8ebwG7uSK1F2vf0N4O2XY4BWjmwr HOeFH3ZA130 assertion
type: Assertion
description: [ Analysis of our data revealed an independent association between the HL gene promoter polymorphisms and HDL-C levels in Taiwanese-Chinese. The data also suggests that the HL-514C/T and HL-250G/A polymorphisms interact with sex and obesity on HDL-C levels. The findings give clues for identifying high risk population in preventive medicine and clinical diagnosis. The subsequent impacts on treatment profiles and prognosis were derived from this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14709367
was generated by: ECO_0000203

NP55333.RAYU5A7O-jDslGqEJ0Ya2DpteBUlrC33LUFOQ ECQ72Jg
has assertion: NP55333.RAYU5A7O-jDslGqEJ0Ya2DpteBUlrC33LUFOQ ECQ72Jg130 assertion
has provenance: NP55333.RAYU5A7O-jDslGqEJ0Ya2DpteBUlrC33LUFOQ ECQ72Jg130 provenance
has publication info: NP55333.RAYU5A7O-jDslGqEJ0Ya2DpteBUlrC33LUFOQ ECQ72Jg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55333.RAYU5A7O-jDslGqEJ0Ya2DpteBUlrC33LUFOQ ECQ72Jg130 assertion
type: Assertion
description: [Although the use of obese-only samples is theoretically a useful approach to detect interactions, few genotype-by-nutrient interactions have been suggested in obese European women after the analysis of candidate polymorphisms and the selected nutrient variables. The most remarkable multiplicative interaction found in this study refers to the combination of the hepatic lipase gene polymorphism -514 C > T and fibre intake.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17080261
was generated by: ECO_0000203

NP55336.RAY32YoxZl9aMozAQXuxVE AmbtwjK xZTAxzkOWoTcwc
has assertion: NP55336.RAY32YoxZl9aMozAQXuxVE AmbtwjK xZTAxzkOWoTcwc130 assertion
has provenance: NP55336.RAY32YoxZl9aMozAQXuxVE AmbtwjK xZTAxzkOWoTcwc130 provenance
has publication info: NP55336.RAY32YoxZl9aMozAQXuxVE AmbtwjK xZTAxzkOWoTcwc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55336.RAY32YoxZl9aMozAQXuxVE AmbtwjK xZTAxzkOWoTcwc130 assertion
type: Assertion
description: [Atorvastatin dose-dependently decreases hepatic lipase activity in type 2 diabetes: effect of sex and the LIPC promoter variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12547874
was generated by: ECO_0000203

NP55344.RASf7i4LhhotrUWoq10bfdWxTjNeCBAjQ6m5HJxZ0J9C8
has assertion: NP55344.RASf7i4LhhotrUWoq10bfdWxTjNeCBAjQ6m5HJxZ0J9C8130 assertion
has provenance: NP55344.RASf7i4LhhotrUWoq10bfdWxTjNeCBAjQ6m5HJxZ0J9C8130 provenance
has publication info: NP55344.RASf7i4LhhotrUWoq10bfdWxTjNeCBAjQ6m5HJxZ0J9C8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55344.RASf7i4LhhotrUWoq10bfdWxTjNeCBAjQ6m5HJxZ0J9C8130 assertion
type: Assertion
description: [The LIPC-480 TT genotype predicted an increase in CHD in both ethnic groups, and physical activity altered this relation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14585761
was generated by: ECO_0000203

NP55345.RAfv6kMMFRlcGU47JHXugtseKQUZP-Q7li-PfbPZjwf7c
has assertion: NP55345.RAfv6kMMFRlcGU47JHXugtseKQUZP-Q7li-PfbPZjwf7c130 assertion
has provenance: NP55345.RAfv6kMMFRlcGU47JHXugtseKQUZP-Q7li-PfbPZjwf7c130 provenance
has publication info: NP55345.RAfv6kMMFRlcGU47JHXugtseKQUZP-Q7li-PfbPZjwf7c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55345.RAfv6kMMFRlcGU47JHXugtseKQUZP-Q7li-PfbPZjwf7c130 assertion
type: Assertion
description: [Association between -514C-->T polymorphism of the hepatic lipase gene and coronary artery disease in a Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18468200
was generated by: ECO_0000203

NP55349.RAakvKpwoTpeE6DHMhyknUkt1vJsBH5viFqUoSdXDYCcc
has assertion: NP55349.RAakvKpwoTpeE6DHMhyknUkt1vJsBH5viFqUoSdXDYCcc130 assertion
has provenance: NP55349.RAakvKpwoTpeE6DHMhyknUkt1vJsBH5viFqUoSdXDYCcc130 provenance
has publication info: NP55349.RAakvKpwoTpeE6DHMhyknUkt1vJsBH5viFqUoSdXDYCcc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55349.RAakvKpwoTpeE6DHMhyknUkt1vJsBH5viFqUoSdXDYCcc130 assertion
type: Assertion
description: [No significant interactions were seen between any of these polymorphisms and duration or dose of cigarette smoking. The gene-environment interaction data suggest that the subtle effects of some of these variants on breast cancer risk may be magnified in the presence of certain exposures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14578164
was generated by: ECO_0000203

NP55353.RATA108JeyuomEbdDU8hePMV5u9H6yZ16D1LecNelxoJ0
has assertion: NP55353.RATA108JeyuomEbdDU8hePMV5u9H6yZ16D1LecNelxoJ0130 assertion
has provenance: NP55353.RATA108JeyuomEbdDU8hePMV5u9H6yZ16D1LecNelxoJ0130 provenance
has publication info: NP55353.RATA108JeyuomEbdDU8hePMV5u9H6yZ16D1LecNelxoJ0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55353.RATA108JeyuomEbdDU8hePMV5u9H6yZ16D1LecNelxoJ0130 assertion
type: Assertion
description: [Pooling data within a large consortium has helped to clarify associations of SNPs with breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17018785
was generated by: ECO_0000203

NP55354.RAQgJKi4v5fVu6DF7zBETP5K00QugF6tvGkQZaO0GJpxw
has assertion: NP55354.RAQgJKi4v5fVu6DF7zBETP5K00QugF6tvGkQZaO0GJpxw130 assertion
has provenance: NP55354.RAQgJKi4v5fVu6DF7zBETP5K00QugF6tvGkQZaO0GJpxw130 provenance
has publication info: NP55354.RAQgJKi4v5fVu6DF7zBETP5K00QugF6tvGkQZaO0GJpxw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55354.RAQgJKi4v5fVu6DF7zBETP5K00QugF6tvGkQZaO0GJpxw130 assertion
type: Assertion
description: [PTGS2 and ERCC5 were associated with stomach cancer risk in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19661089
was generated by: ECO_0000203

NP55356.RATffAH6wmRN7C4MUkqf-7oLIFwmBub8cz39qnQAdZPv4
has assertion: NP55356.RATffAH6wmRN7C4MUkqf-7oLIFwmBub8cz39qnQAdZPv4130 assertion
has provenance: NP55356.RATffAH6wmRN7C4MUkqf-7oLIFwmBub8cz39qnQAdZPv4130 provenance
has publication info: NP55356.RATffAH6wmRN7C4MUkqf-7oLIFwmBub8cz39qnQAdZPv4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55356.RATffAH6wmRN7C4MUkqf-7oLIFwmBub8cz39qnQAdZPv4130 assertion
type: Assertion
description: [ILT6 deficiency is associated with MS in the German population and hence a likely risk factor for autoimmune disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15815690
was generated by: ECO_0000203

NP55357.RASNBJCIoTfvZKfAuMUOdowN6Oyi7WR-11BEQWa7FCq8E
has assertion: NP55357.RASNBJCIoTfvZKfAuMUOdowN6Oyi7WR-11BEQWa7FCq8E130 assertion
has provenance: NP55357.RASNBJCIoTfvZKfAuMUOdowN6Oyi7WR-11BEQWa7FCq8E130 provenance
has publication info: NP55357.RASNBJCIoTfvZKfAuMUOdowN6Oyi7WR-11BEQWa7FCq8E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55357.RASNBJCIoTfvZKfAuMUOdowN6Oyi7WR-11BEQWa7FCq8E130 assertion
type: Assertion
description: [Our study points to a gene-dose-dependent, protective role for LILRA3, the deletion of which synergizes with HLA-DRB1(*)1501 to increase the risk of R-MS. We also investigated whether the risk of suffering R-MS might be influenced by the genotypic diversity of killer-cell Ig-like receptors (KIRs), located only approximately 400 kb telomeric to LILRA3, and implicated in autoimmunity and defence against viruses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19421224
was generated by: ECO_0000203

NP55363.RAZsiLMzsvb1-paLMCrYOGGui cEuta0JR9WwwBpl3FMY
has assertion: NP55363.RAZsiLMzsvb1-paLMCrYOGGui cEuta0JR9WwwBpl3FMY130 assertion
has provenance: NP55363.RAZsiLMzsvb1-paLMCrYOGGui cEuta0JR9WwwBpl3FMY130 provenance
has publication info: NP55363.RAZsiLMzsvb1-paLMCrYOGGui cEuta0JR9WwwBpl3FMY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55363.RAZsiLMzsvb1-paLMCrYOGGui cEuta0JR9WwwBpl3FMY130 assertion
type: Assertion
description: [ Our findings suggest that genetic polymorphisms of RAD52, ERCC1, and hMLH1 may be associated with breast cancer risk in Korean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15958648
was generated by: ECO_0000203

NP55372.RAT9TJ1TH6tP680x7znT5MdMSQaA1AWgPo7wPXMTezTYg
has assertion: NP55372.RAT9TJ1TH6tP680x7znT5MdMSQaA1AWgPo7wPXMTezTYg130 assertion
has provenance: NP55372.RAT9TJ1TH6tP680x7znT5MdMSQaA1AWgPo7wPXMTezTYg130 provenance
has publication info: NP55372.RAT9TJ1TH6tP680x7znT5MdMSQaA1AWgPo7wPXMTezTYg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55372.RAT9TJ1TH6tP680x7znT5MdMSQaA1AWgPo7wPXMTezTYg130 assertion
type: Assertion
description: [A genotypic association was found for the c.1914GC --> AT polymorphism in 42 CAE patients compared with 110 population controls (chi2 = 6.66, df = 1, P = 0.01), providing evidence for a so far undetected susceptibility allele for CAE in the LGI4 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14505228
was generated by: ECO_0000203

NP55377.RAXEY5O4GqO4yFyK9Hcidd7GFc0O2m1AkH9xAcsohYMHg
has assertion: NP55377.RAXEY5O4GqO4yFyK9Hcidd7GFc0O2m1AkH9xAcsohYMHg130 assertion
has provenance: NP55377.RAXEY5O4GqO4yFyK9Hcidd7GFc0O2m1AkH9xAcsohYMHg130 provenance
has publication info: NP55377.RAXEY5O4GqO4yFyK9Hcidd7GFc0O2m1AkH9xAcsohYMHg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55377.RAXEY5O4GqO4yFyK9Hcidd7GFc0O2m1AkH9xAcsohYMHg130 assertion
type: Assertion
description: [our results show that a common variant in LEP may be associated with the risk of developing breast cancer supporting the hypothesis that leptin is involved in breast carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19697123
was generated by: ECO_0000203

NP55381.RAdm0G1u7odw6LpvHSawyiQ-15eYh80RzHp0UYdXbK9lc
has assertion: NP55381.RAdm0G1u7odw6LpvHSawyiQ-15eYh80RzHp0UYdXbK9lc130 assertion
has provenance: NP55381.RAdm0G1u7odw6LpvHSawyiQ-15eYh80RzHp0UYdXbK9lc130 provenance
has publication info: NP55381.RAdm0G1u7odw6LpvHSawyiQ-15eYh80RzHp0UYdXbK9lc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55381.RAdm0G1u7odw6LpvHSawyiQ-15eYh80RzHp0UYdXbK9lc130 assertion
type: Assertion
description: [In Caucasians, LEP SNPs also tended to be associated with weight (p = 0.0471), and PYY rs11684664 was associated with obesity-related phenotypes in women only (p = 0.010-0.026).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20642810
was generated by: ECO_0000203

NP55386.RATA64M1sIq8hm06 2 XOWY1qwvF-STDpXBZo2CPArH8o
has assertion: NP55386.RATA64M1sIq8hm06 2 XOWY1qwvF-STDpXBZo2CPArH8o130 assertion
has provenance: NP55386.RATA64M1sIq8hm06 2 XOWY1qwvF-STDpXBZo2CPArH8o130 provenance
has publication info: NP55386.RATA64M1sIq8hm06 2 XOWY1qwvF-STDpXBZo2CPArH8o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55386.RATA64M1sIq8hm06 2 XOWY1qwvF-STDpXBZo2CPArH8o130 assertion
type: Assertion
description: [This study provides basic information concerning the prevalence of leptin gene polymorphisms in Thai children with early onset obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20232565
was generated by: ECO_0000203

NP55389.RAQSHDXtdg7GEf1qKv3ZMjLHukA1GxOJG8 N9p6LQZOd8
has assertion: NP55389.RAQSHDXtdg7GEf1qKv3ZMjLHukA1GxOJG8 N9p6LQZOd8130 assertion
has provenance: NP55389.RAQSHDXtdg7GEf1qKv3ZMjLHukA1GxOJG8 N9p6LQZOd8130 provenance
has publication info: NP55389.RAQSHDXtdg7GEf1qKv3ZMjLHukA1GxOJG8 N9p6LQZOd8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55389.RAQSHDXtdg7GEf1qKv3ZMjLHukA1GxOJG8 N9p6LQZOd8130 assertion
type: Assertion
description: [Larger studies would be needed to confirm and further clarify the relations between functional variants in the leptin gene and preeclampsia risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15544427
was generated by: ECO_0000203

NP55393.RAQEb hFWMM8z9n0tbW4yaRFP9dvS5LK-dQVhBOBlIzG0
has assertion: NP55393.RAQEb hFWMM8z9n0tbW4yaRFP9dvS5LK-dQVhBOBlIzG0130 assertion
has provenance: NP55393.RAQEb hFWMM8z9n0tbW4yaRFP9dvS5LK-dQVhBOBlIzG0130 provenance
has publication info: NP55393.RAQEb hFWMM8z9n0tbW4yaRFP9dvS5LK-dQVhBOBlIzG0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55393.RAQEb hFWMM8z9n0tbW4yaRFP9dvS5LK-dQVhBOBlIzG0130 assertion
type: Assertion
description: [ According to our results we hypothesize that the polymorphism in LEP gene may be relevant to PC risk and progression, supporting the hypothesis for leptin involvement in cancer ethiopathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15042602
was generated by: ECO_0000203

NP55395.RAUJhqZyOXmEtCkTyy60Tk6YMqXyP3StOOXohnnOY3kk0
has assertion: NP55395.RAUJhqZyOXmEtCkTyy60Tk6YMqXyP3StOOXohnnOY3kk0130 assertion
has provenance: NP55395.RAUJhqZyOXmEtCkTyy60Tk6YMqXyP3StOOXohnnOY3kk0130 provenance
has publication info: NP55395.RAUJhqZyOXmEtCkTyy60Tk6YMqXyP3StOOXohnnOY3kk0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55395.RAUJhqZyOXmEtCkTyy60Tk6YMqXyP3StOOXohnnOY3kk0130 assertion
type: Assertion
description: [Our prospective study suggests that genetic variation in IL10 and possibly TLR4 is associated with prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19267370
was generated by: ECO_0000203

NP55401.RARiA88QuTsBgkZ6it2k8Sez8uAD8aTLqYrWLaJQT00FE
has assertion: NP55401.RARiA88QuTsBgkZ6it2k8Sez8uAD8aTLqYrWLaJQT00FE130 assertion
has provenance: NP55401.RARiA88QuTsBgkZ6it2k8Sez8uAD8aTLqYrWLaJQT00FE130 provenance
has publication info: NP55401.RARiA88QuTsBgkZ6it2k8Sez8uAD8aTLqYrWLaJQT00FE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55401.RARiA88QuTsBgkZ6it2k8Sez8uAD8aTLqYrWLaJQT00FE130 assertion
type: Assertion
description: [ These results suggest that no mutations in either the promoter region at the about 100 bp 5'-flanking region of the gene, or in any of the three exons, are involved in the development of NIDDM or IGT associated with obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9405031
was generated by: ECO_0000203

NP55403.RAY7wr4r1E014UJL63vUlfikE0L2vbEsdqmotdR-Bzy44
has assertion: NP55403.RAY7wr4r1E014UJL63vUlfikE0L2vbEsdqmotdR-Bzy44130 assertion
has provenance: NP55403.RAY7wr4r1E014UJL63vUlfikE0L2vbEsdqmotdR-Bzy44130 provenance
has publication info: NP55403.RAY7wr4r1E014UJL63vUlfikE0L2vbEsdqmotdR-Bzy44130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55403.RAY7wr4r1E014UJL63vUlfikE0L2vbEsdqmotdR-Bzy44130 assertion
type: Assertion
description: [In conclusion, we observed that several polymorphisms in LEPR that had previous reports of association with BMI were significantly replicated in our samples and newly found that some variations of LEP were associated with T2DM and metabolic traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18564365
was generated by: ECO_0000203

NP55404.RAc GtUf5u Pb8X5YD3JabGgfCLIFm eDRzKOE4ZbsskI
has assertion: NP55404.RAc GtUf5u Pb8X5YD3JabGgfCLIFm eDRzKOE4ZbsskI130 assertion
has provenance: NP55404.RAc GtUf5u Pb8X5YD3JabGgfCLIFm eDRzKOE4ZbsskI130 provenance
has publication info: NP55404.RAc GtUf5u Pb8X5YD3JabGgfCLIFm eDRzKOE4ZbsskI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55404.RAc GtUf5u Pb8X5YD3JabGgfCLIFm eDRzKOE4ZbsskI130 assertion
type: Assertion
description: [Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: linkage of candidate genes using two sib-pair based variance components analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18828733
was generated by: ECO_0000203

NP55408.RATwj7MlaHBp5nbbUIPAQiWyt-hPZ-K4tO3BmYWhTQcDQ
has assertion: NP55408.RATwj7MlaHBp5nbbUIPAQiWyt-hPZ-K4tO3BmYWhTQcDQ130 assertion
has provenance: NP55408.RATwj7MlaHBp5nbbUIPAQiWyt-hPZ-K4tO3BmYWhTQcDQ130 provenance
has publication info: NP55408.RATwj7MlaHBp5nbbUIPAQiWyt-hPZ-K4tO3BmYWhTQcDQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55408.RATwj7MlaHBp5nbbUIPAQiWyt-hPZ-K4tO3BmYWhTQcDQ130 assertion
type: Assertion
description: [Adjustment for LDL-C levels by logistic regression or Mendelian Randomisation models abolished the significant association between rs2228671 with CAD completely, indicating a functional link between the genetic variant at the LDLR gene locus, change in LDL-C and risk of CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18714375
was generated by: ECO_0000203

NP55411.RAZJloommRZjFF8h0Xquc1xRT3y3wOJhR Ud90ORQ-29A
has assertion: NP55411.RAZJloommRZjFF8h0Xquc1xRT3y3wOJhR Ud90ORQ-29A130 assertion
has provenance: NP55411.RAZJloommRZjFF8h0Xquc1xRT3y3wOJhR Ud90ORQ-29A130 provenance
has publication info: NP55411.RAZJloommRZjFF8h0Xquc1xRT3y3wOJhR Ud90ORQ-29A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55411.RAZJloommRZjFF8h0Xquc1xRT3y3wOJhR Ud90ORQ-29A130 assertion
type: Assertion
description: [ Our data indicate that ChM-II Val58Ile polymorphism is associated with radiographic progression of joint destruction, particularly in German patients with RA negative for SE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16142856
was generated by: ECO_0000203

NP55412.RAawE2N3EyptsObCHGxbUu2r9RHe9RTOk6S93kaPijK6E
has assertion: NP55412.RAawE2N3EyptsObCHGxbUu2r9RHe9RTOk6S93kaPijK6E130 assertion
has provenance: NP55412.RAawE2N3EyptsObCHGxbUu2r9RHe9RTOk6S93kaPijK6E130 provenance
has publication info: NP55412.RAawE2N3EyptsObCHGxbUu2r9RHe9RTOk6S93kaPijK6E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55412.RAawE2N3EyptsObCHGxbUu2r9RHe9RTOk6S93kaPijK6E130 assertion
type: Assertion
description: [Novel mutations identification in exon 4 of LDLR gene in patients with moderate hypercholesterolemia in a Venezuelan population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20019594
was generated by: ECO_0000203

NP55420.RAbDdW7aYukKLLvR3 E8Cq3xXAK8ihnxvZVkwlfS3rxwU
has assertion: NP55420.RAbDdW7aYukKLLvR3 E8Cq3xXAK8ihnxvZVkwlfS3rxwU130 assertion
has provenance: NP55420.RAbDdW7aYukKLLvR3 E8Cq3xXAK8ihnxvZVkwlfS3rxwU130 provenance
has publication info: NP55420.RAbDdW7aYukKLLvR3 E8Cq3xXAK8ihnxvZVkwlfS3rxwU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55420.RAbDdW7aYukKLLvR3 E8Cq3xXAK8ihnxvZVkwlfS3rxwU130 assertion
type: Assertion
description: [A total of 118 FH subjects could be classified into three groups according to the type of LDLR mutations (null mutations, missense mutations affecting the ligand binding 3-5 repeat, and missense mutations outside this domain).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14508510
was generated by: ECO_0000203

NP55422.RAZTKPkRNpQdG2Z-Z4xh-kzqVG2ztLHecE0OFaYZmktTY
has assertion: NP55422.RAZTKPkRNpQdG2Z-Z4xh-kzqVG2ztLHecE0OFaYZmktTY130 assertion
has provenance: NP55422.RAZTKPkRNpQdG2Z-Z4xh-kzqVG2ztLHecE0OFaYZmktTY130 provenance
has publication info: NP55422.RAZTKPkRNpQdG2Z-Z4xh-kzqVG2ztLHecE0OFaYZmktTY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55422.RAZTKPkRNpQdG2Z-Z4xh-kzqVG2ztLHecE0OFaYZmktTY130 assertion
type: Assertion
description: [To evaluate the relationship between low density lipoprotein receptor (LDLR) genetic variant and AD, independently or in concert with the APOE epsilon4 allele, we examined three LDLR polymorphisms located in exons 8 (rs 11669576), 10 (rs 5930), and 13 (rs 5925), in a large group of 322 Spanish AD patients and 314 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16741934
was generated by: ECO_0000203

NP55429.RAc54l4Q0o12O5HL379iUpFd89Z0cn1Hshqi4W3Csnpa4
has assertion: NP55429.RAc54l4Q0o12O5HL379iUpFd89Z0cn1Hshqi4W3Csnpa4130 assertion
has provenance: NP55429.RAc54l4Q0o12O5HL379iUpFd89Z0cn1Hshqi4W3Csnpa4130 provenance
has publication info: NP55429.RAc54l4Q0o12O5HL379iUpFd89Z0cn1Hshqi4W3Csnpa4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55429.RAc54l4Q0o12O5HL379iUpFd89Z0cn1Hshqi4W3Csnpa4130 assertion
type: Assertion
description: [odds ratios.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16378661
was generated by: ECO_0000203

NP55430.RAZqtMZFCdykafOWQ8Plci7B8GobgPomtgx1wcfc0jbNU
has assertion: NP55430.RAZqtMZFCdykafOWQ8Plci7B8GobgPomtgx1wcfc0jbNU130 assertion
has provenance: NP55430.RAZqtMZFCdykafOWQ8Plci7B8GobgPomtgx1wcfc0jbNU130 provenance
has publication info: NP55430.RAZqtMZFCdykafOWQ8Plci7B8GobgPomtgx1wcfc0jbNU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55430.RAZqtMZFCdykafOWQ8Plci7B8GobgPomtgx1wcfc0jbNU130 assertion
type: Assertion
description: [Functional interaction between APOE4 and LDL receptor isoforms in Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15689450
was generated by: ECO_0000203

NP55444.RAW7TSVlqW-oV9-xQ-FTWw-pCrrGVQc hnR1bSuQv 6cE
has assertion: NP55444.RAW7TSVlqW-oV9-xQ-FTWw-pCrrGVQc hnR1bSuQv 6cE130 assertion
has provenance: NP55444.RAW7TSVlqW-oV9-xQ-FTWw-pCrrGVQc hnR1bSuQv 6cE130 provenance
has publication info: NP55444.RAW7TSVlqW-oV9-xQ-FTWw-pCrrGVQc hnR1bSuQv 6cE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55444.RAW7TSVlqW-oV9-xQ-FTWw-pCrrGVQc hnR1bSuQv 6cE130 assertion
type: Assertion
description: [We investigated the LDLR gene mutations in 205 unrelated Japanese FH (familial hypercholesterolemia) heterozygotes to see if there is a prevalence of common mutations in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18718593
was generated by: ECO_0000203

NP55450.RATnQWQDoj69mquRX2awpU7wtg8pya6t5Wbvoq-4HWzc8
has assertion: NP55450.RATnQWQDoj69mquRX2awpU7wtg8pya6t5Wbvoq-4HWzc8130 assertion
has provenance: NP55450.RATnQWQDoj69mquRX2awpU7wtg8pya6t5Wbvoq-4HWzc8130 provenance
has publication info: NP55450.RATnQWQDoj69mquRX2awpU7wtg8pya6t5Wbvoq-4HWzc8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55450.RATnQWQDoj69mquRX2awpU7wtg8pya6t5Wbvoq-4HWzc8130 assertion
type: Assertion
description: [Two new large deletions in the low density lipoprotein receptor (LDLR) gene not revealed by PCR-based molecular diagnosis of familial hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17399720
was generated by: ECO_0000203

NP55453.RAdywJcfGlt8GUZ1YlTOdLt3rAsaSuVd5IbYG5agE7uUc
has assertion: NP55453.RAdywJcfGlt8GUZ1YlTOdLt3rAsaSuVd5IbYG5agE7uUc130 assertion
has provenance: NP55453.RAdywJcfGlt8GUZ1YlTOdLt3rAsaSuVd5IbYG5agE7uUc130 provenance
has publication info: NP55453.RAdywJcfGlt8GUZ1YlTOdLt3rAsaSuVd5IbYG5agE7uUc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55453.RAdywJcfGlt8GUZ1YlTOdLt3rAsaSuVd5IbYG5agE7uUc130 assertion
type: Assertion
description: [The present study therefore adds to our previous evidence implicating LDLR as a locus for obesity in patients with essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/7634533
was generated by: ECO_0000203

NP55454.RAQ7i1bK6ptocSXHuGcRMpyorYgapM0FPn NfBUYWRN5E
has assertion: NP55454.RAQ7i1bK6ptocSXHuGcRMpyorYgapM0FPn NfBUYWRN5E130 assertion
has provenance: NP55454.RAQ7i1bK6ptocSXHuGcRMpyorYgapM0FPn NfBUYWRN5E130 provenance
has publication info: NP55454.RAQ7i1bK6ptocSXHuGcRMpyorYgapM0FPn NfBUYWRN5E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55454.RAQ7i1bK6ptocSXHuGcRMpyorYgapM0FPn NfBUYWRN5E130 assertion
type: Assertion
description: [Marked association of a RFLP for the low density lipoprotein receptor gene with obesity in essential hypertensives.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/1361731
was generated by: ECO_0000203

NP55458.RAbfFhw8dqRI7lZjumYBhWB9a4QlQ4YgqIO1Fh oItyys
has assertion: NP55458.RAbfFhw8dqRI7lZjumYBhWB9a4QlQ4YgqIO1Fh oItyys130 assertion
has provenance: NP55458.RAbfFhw8dqRI7lZjumYBhWB9a4QlQ4YgqIO1Fh oItyys130 provenance
has publication info: NP55458.RAbfFhw8dqRI7lZjumYBhWB9a4QlQ4YgqIO1Fh oItyys130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55458.RAbfFhw8dqRI7lZjumYBhWB9a4QlQ4YgqIO1Fh oItyys130 assertion
type: Assertion
description: [Investigation of an LDLR gene polymorphism (19p13.2) in susceptibility to migraine without aura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12873747
was generated by: ECO_0000203

NP55463.RAUICeZ0iyES4MscjUBrRmGGlRKeIv40T9DhAcuRN1XGQ
has assertion: NP55463.RAUICeZ0iyES4MscjUBrRmGGlRKeIv40T9DhAcuRN1XGQ130 assertion
has provenance: NP55463.RAUICeZ0iyES4MscjUBrRmGGlRKeIv40T9DhAcuRN1XGQ130 provenance
has publication info: NP55463.RAUICeZ0iyES4MscjUBrRmGGlRKeIv40T9DhAcuRN1XGQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55463.RAUICeZ0iyES4MscjUBrRmGGlRKeIv40T9DhAcuRN1XGQ130 assertion
type: Assertion
description: [In the Italian population the LCT-13910C>T polymorphism is not associated to the risk for colorectal cancer or polyps.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20362522
was generated by: ECO_0000203

NP55464.RAWarBTT6pWBy9 lN5g7cOBPs-DUKV2FdHWhlRTnjFpKM
has assertion: NP55464.RAWarBTT6pWBy9 lN5g7cOBPs-DUKV2FdHWhlRTnjFpKM130 assertion
has provenance: NP55464.RAWarBTT6pWBy9 lN5g7cOBPs-DUKV2FdHWhlRTnjFpKM130 provenance
has publication info: NP55464.RAWarBTT6pWBy9 lN5g7cOBPs-DUKV2FdHWhlRTnjFpKM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55464.RAWarBTT6pWBy9 lN5g7cOBPs-DUKV2FdHWhlRTnjFpKM130 assertion
type: Assertion
description: [The authors validate a denaturing high-performance liquid chromatography (dHPLC)-based assay versus conventional genotype sequencing in detecting the C/T(-13910) polymorphism of LCT and evaluate its prevalence in 2 different Italian geographical areas and in colorectal cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17478481
was generated by: ECO_0000203

NP55469.RAdUBkrpYeV Ko5t4jxLMb02PClNxSmaDrBjxM5ApznzU
has assertion: NP55469.RAdUBkrpYeV Ko5t4jxLMb02PClNxSmaDrBjxM5ApznzU130 assertion
has provenance: NP55469.RAdUBkrpYeV Ko5t4jxLMb02PClNxSmaDrBjxM5ApznzU130 provenance
has publication info: NP55469.RAdUBkrpYeV Ko5t4jxLMb02PClNxSmaDrBjxM5ApznzU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55469.RAdUBkrpYeV Ko5t4jxLMb02PClNxSmaDrBjxM5ApznzU130 assertion
type: Assertion
description: [We have demonstrated that the lysosome associated membrane protein (LAMP-1) is elevated in plasma from approximately 70% of lysosomal storage disorder patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11400745
was generated by: ECO_0000203

NP55470.RAV 5EA903JmixZA9f3iD FXuiNupou7uavNbVxz46ZaQ
has assertion: NP55470.RAV 5EA903JmixZA9f3iD FXuiNupou7uavNbVxz46ZaQ130 assertion
has provenance: NP55470.RAV 5EA903JmixZA9f3iD FXuiNupou7uavNbVxz46ZaQ130 provenance
has publication info: NP55470.RAV 5EA903JmixZA9f3iD FXuiNupou7uavNbVxz46ZaQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55470.RAV 5EA903JmixZA9f3iD FXuiNupou7uavNbVxz46ZaQ130 assertion
type: Assertion
description: [This study suggests that the allele *2 of LAPTM4B might be the risk factor of lung cancer, which could be associated with genetic susceptibility of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15968325
was generated by: ECO_0000203

NP55479.RASzxj6Zpj3voiPbprt5wh3qfBie-wm2TYIuymAKxg8c4
has assertion: NP55479.RASzxj6Zpj3voiPbprt5wh3qfBie-wm2TYIuymAKxg8c4130 assertion
has provenance: NP55479.RASzxj6Zpj3voiPbprt5wh3qfBie-wm2TYIuymAKxg8c4130 provenance
has publication info: NP55479.RASzxj6Zpj3voiPbprt5wh3qfBie-wm2TYIuymAKxg8c4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55479.RASzxj6Zpj3voiPbprt5wh3qfBie-wm2TYIuymAKxg8c4130 assertion
type: Assertion
description: [These results suggest that the polymorphism in intron 25 plays a role in the genetic predisposition of male schizophrenia in the Japanese sample]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11425011
was generated by: ECO_0000203

NP55492.RAXdJEDM4G78CAobeJTwlnpW-sDwQQ37xe5kvqUKot-Ak
has assertion: NP55492.RAXdJEDM4G78CAobeJTwlnpW-sDwQQ37xe5kvqUKot-Ak130 assertion
has provenance: NP55492.RAXdJEDM4G78CAobeJTwlnpW-sDwQQ37xe5kvqUKot-Ak130 provenance
has publication info: NP55492.RAXdJEDM4G78CAobeJTwlnpW-sDwQQ37xe5kvqUKot-Ak130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55492.RAXdJEDM4G78CAobeJTwlnpW-sDwQQ37xe5kvqUKot-Ak130 assertion
type: Assertion
description: [While we were able to replicate a few of the previous GWAS SNPs, we were not able to confirm the vast majority of these associations in our AA population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19902474
was generated by: ECO_0000203

NP55494.RAZ W6sz0Lbc9VdRmO9V-YSzpaXFTb6zeZC57Yoxu3BDc
has assertion: NP55494.RAZ W6sz0Lbc9VdRmO9V-YSzpaXFTb6zeZC57Yoxu3BDc130 assertion
has provenance: NP55494.RAZ W6sz0Lbc9VdRmO9V-YSzpaXFTb6zeZC57Yoxu3BDc130 provenance
has publication info: NP55494.RAZ W6sz0Lbc9VdRmO9V-YSzpaXFTb6zeZC57Yoxu3BDc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55494.RAZ W6sz0Lbc9VdRmO9V-YSzpaXFTb6zeZC57Yoxu3BDc130 assertion
type: Assertion
description: [From 1990 through 2000, urologic measures of BPH were assessed biennially from lower urinary tract symptom severity, peak flow rates, prostate volume, serum prostate specific antigen (PSA) level, acute urinary retention, and treatment for BPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16302261
was generated by: ECO_0000203

NP55495.RAWABBLtAzcuLp3O yLZuo5w1ePBSWhe16 1BZeaR7yYo
has assertion: NP55495.RAWABBLtAzcuLp3O yLZuo5w1ePBSWhe16 1BZeaR7yYo130 assertion
has provenance: NP55495.RAWABBLtAzcuLp3O yLZuo5w1ePBSWhe16 1BZeaR7yYo130 provenance
has publication info: NP55495.RAWABBLtAzcuLp3O yLZuo5w1ePBSWhe16 1BZeaR7yYo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55495.RAWABBLtAzcuLp3O yLZuo5w1ePBSWhe16 1BZeaR7yYo130 assertion
type: Assertion
description: [Androgen receptor and prostate-specific antigen gene polymorphisms and breast cancer in African-American women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16365023
was generated by: ECO_0000203

NP55497.RAZiBph-Qg-0Fxk2kuMFQihlZIcRs-OB-ilbM8UNunWvs
has assertion: NP55497.RAZiBph-Qg-0Fxk2kuMFQihlZIcRs-OB-ilbM8UNunWvs130 assertion
has provenance: NP55497.RAZiBph-Qg-0Fxk2kuMFQihlZIcRs-OB-ilbM8UNunWvs130 provenance
has publication info: NP55497.RAZiBph-Qg-0Fxk2kuMFQihlZIcRs-OB-ilbM8UNunWvs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55497.RAZiBph-Qg-0Fxk2kuMFQihlZIcRs-OB-ilbM8UNunWvs130 assertion
type: Assertion
description: [When combined, the adjusted odds ratio for having prostate cancer was 13.92 (95% CI, 6.6 to 29.2; P =.0001) for patients with high hK2 levels and at least one T allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12805332
was generated by: ECO_0000203

NP55499.RAR3Ygi-KPqvcrjgauKBiyH9hfPlxdlRM2vHs4FbRCTQc
has assertion: NP55499.RAR3Ygi-KPqvcrjgauKBiyH9hfPlxdlRM2vHs4FbRCTQc130 assertion
has provenance: NP55499.RAR3Ygi-KPqvcrjgauKBiyH9hfPlxdlRM2vHs4FbRCTQc130 provenance
has publication info: NP55499.RAR3Ygi-KPqvcrjgauKBiyH9hfPlxdlRM2vHs4FbRCTQc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55499.RAR3Ygi-KPqvcrjgauKBiyH9hfPlxdlRM2vHs4FbRCTQc130 assertion
type: Assertion
description: [These findings suggest a role for the KLK2 gene in prostate cancer susceptibility and imply that this role may be realized at least in part by the induction of increases in hK2 production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17085659
was generated by: ECO_0000203

NP55506.RATsmg0Wt 1jmfdtB4vL64v7XjM5Ki87BdQlH4BFLLLsk
has assertion: NP55506.RATsmg0Wt 1jmfdtB4vL64v7XjM5Ki87BdQlH4BFLLLsk130 assertion
has provenance: NP55506.RATsmg0Wt 1jmfdtB4vL64v7XjM5Ki87BdQlH4BFLLLsk130 provenance
has publication info: NP55506.RATsmg0Wt 1jmfdtB4vL64v7XjM5Ki87BdQlH4BFLLLsk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55506.RATsmg0Wt 1jmfdtB4vL64v7XjM5Ki87BdQlH4BFLLLsk130 assertion
type: Assertion
description: [Blood biomarker levels to aid discovery of cancer-related single-nucleotide polymorphisms: kallikreins and prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20424135
was generated by: ECO_0000203

NP55507.RATyLzMKUGa4PiGaISE4bKHVN90BPyk9wPCPU9yu0o25M
has assertion: NP55507.RATyLzMKUGa4PiGaISE4bKHVN90BPyk9wPCPU9yu0o25M130 assertion
has provenance: NP55507.RATyLzMKUGa4PiGaISE4bKHVN90BPyk9wPCPU9yu0o25M130 provenance
has publication info: NP55507.RATyLzMKUGa4PiGaISE4bKHVN90BPyk9wPCPU9yu0o25M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55507.RATyLzMKUGa4PiGaISE4bKHVN90BPyk9wPCPU9yu0o25M130 assertion
type: Assertion
description: [B2 receptor promoter polymorphism may represent a susceptibility marker for essential hypertension in African-Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11130770
was generated by: ECO_0000203

NP55508.RAXb69YHr5yn8xs BVCVST60fAk22VbpmMvtJyVZ9CLIw
has assertion: NP55508.RAXb69YHr5yn8xs BVCVST60fAk22VbpmMvtJyVZ9CLIw130 assertion
has provenance: NP55508.RAXb69YHr5yn8xs BVCVST60fAk22VbpmMvtJyVZ9CLIw130 provenance
has publication info: NP55508.RAXb69YHr5yn8xs BVCVST60fAk22VbpmMvtJyVZ9CLIw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55508.RAXb69YHr5yn8xs BVCVST60fAk22VbpmMvtJyVZ9CLIw130 assertion
type: Assertion
description: [Favorable prognostic value of tissue human kallikrein 11 (hK11) in patients with ovarian carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12845660
was generated by: ECO_0000203

NP55510.RAYCAbMvY125KSGB1fi94Pf6JgubF3J6ytzgDqiWhPN0w
has assertion: NP55510.RAYCAbMvY125KSGB1fi94Pf6JgubF3J6ytzgDqiWhPN0w130 assertion
has provenance: NP55510.RAYCAbMvY125KSGB1fi94Pf6JgubF3J6ytzgDqiWhPN0w130 provenance
has publication info: NP55510.RAYCAbMvY125KSGB1fi94Pf6JgubF3J6ytzgDqiWhPN0w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55510.RAYCAbMvY125KSGB1fi94Pf6JgubF3J6ytzgDqiWhPN0w130 assertion
type: Assertion
description: [In this study, we examined 50 non-cancerous tissues from Japanese patients with primary gastric cancer to determine the presence of genetic polymorphisms in the KLK12 gene using polymerase chain reaction (PCR)-single-strand conformation polymorphism and sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15300858
was generated by: ECO_0000203

NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM
has assertion: NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130 assertion
has provenance: NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130 provenance
has publication info: NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130 assertion
type: Assertion
description: [In conclusion, there are polymorphisms in the regulatory region of human tissue kallikrein gene in the Chinese Han people. Differences in both allele frequencies and genotype frequencies between these two groups have provided evidence towards the association of hypertension with the polymorphisms in this studied site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15905889
was generated by: ECO_0000203

NP55519.RAQcSvmXF7Nfr-JBn3IxeBbkU1fg88-yRtvcVWnQVyx7k
has assertion: NP55519.RAQcSvmXF7Nfr-JBn3IxeBbkU1fg88-yRtvcVWnQVyx7k130 assertion
has provenance: NP55519.RAQcSvmXF7Nfr-JBn3IxeBbkU1fg88-yRtvcVWnQVyx7k130 provenance
has publication info: NP55519.RAQcSvmXF7Nfr-JBn3IxeBbkU1fg88-yRtvcVWnQVyx7k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55519.RAQcSvmXF7Nfr-JBn3IxeBbkU1fg88-yRtvcVWnQVyx7k130 assertion
type: Assertion
description: [These results indicate that the gene encoding KLF7 is a novel candidate for conferring genetic susceptibility to type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15937668
was generated by: ECO_0000203

NP55520.RAY5YVa 6ZbsPFJmYUEFuKtcSjfLQmwa-B2ZUFBVJh7E
has assertion: NP55520.RAY5YVa 6ZbsPFJmYUEFuKtcSjfLQmwa-B2ZUFBVJh7E130 assertion
has provenance: NP55520.RAY5YVa 6ZbsPFJmYUEFuKtcSjfLQmwa-B2ZUFBVJh7E130 provenance
has publication info: NP55520.RAY5YVa 6ZbsPFJmYUEFuKtcSjfLQmwa-B2ZUFBVJh7E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55520.RAY5YVa 6ZbsPFJmYUEFuKtcSjfLQmwa-B2ZUFBVJh7E130 assertion
type: Assertion
description: [It is unlikely that variants in different members of the KLF gene family play a major role in T2D in the French population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17688680
was generated by: ECO_0000203

NP55528.RAbQgQnJOeeFWYwoAa2X6PVz0bW5UGXsqvZHSR8nbGAxY
has assertion: NP55528.RAbQgQnJOeeFWYwoAa2X6PVz0bW5UGXsqvZHSR8nbGAxY130 assertion
has provenance: NP55528.RAbQgQnJOeeFWYwoAa2X6PVz0bW5UGXsqvZHSR8nbGAxY130 provenance
has publication info: NP55528.RAbQgQnJOeeFWYwoAa2X6PVz0bW5UGXsqvZHSR8nbGAxY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55528.RAbQgQnJOeeFWYwoAa2X6PVz0bW5UGXsqvZHSR8nbGAxY130 assertion
type: Assertion
description: [It is unlikely that variants in different members of the KLF gene family play a major role in T2D in the French population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17688680
was generated by: ECO_0000203

NP55530.RAbzfDd0Lzd-o4RpR5O5W7ycLWcD9zDMf7TYXcxwLtFOk
has assertion: NP55530.RAbzfDd0Lzd-o4RpR5O5W7ycLWcD9zDMf7TYXcxwLtFOk130 assertion
has provenance: NP55530.RAbzfDd0Lzd-o4RpR5O5W7ycLWcD9zDMf7TYXcxwLtFOk130 provenance
has publication info: NP55530.RAbzfDd0Lzd-o4RpR5O5W7ycLWcD9zDMf7TYXcxwLtFOk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55530.RAbzfDd0Lzd-o4RpR5O5W7ycLWcD9zDMf7TYXcxwLtFOk130 assertion
type: Assertion
description: [These results indicate that the gene encoding KLF7 is a novel candidate for conferring genetic susceptibility to type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15937668
was generated by: ECO_0000203

NP55534.RAfkb6fcyZV-Cv h4J2a 1DYrNeV2pvlup DbCI1fRdc4
has assertion: NP55534.RAfkb6fcyZV-Cv h4J2a 1DYrNeV2pvlup DbCI1fRdc4130 assertion
has provenance: NP55534.RAfkb6fcyZV-Cv h4J2a 1DYrNeV2pvlup DbCI1fRdc4130 provenance
has publication info: NP55534.RAfkb6fcyZV-Cv h4J2a 1DYrNeV2pvlup DbCI1fRdc4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55534.RAfkb6fcyZV-Cv h4J2a 1DYrNeV2pvlup DbCI1fRdc4130 assertion
type: Assertion
description: [We observed the frequencies of single nucleotide polymorphisms, that is, G-395A in the promoter region, C1818T in exon 4, and a functional variant, KL-VS, of KLOTHO gene in Koreans, and we investigated their relationships with the presence of coronary artery disease (CAD) in patients who had undergone coronary angiograms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16979405
was generated by: ECO_0000203

NP55535.RAZGPP5SJpSF95lOl3-C u5Lvl4zPBDwdGgkpAdqgbMe0
has assertion: NP55535.RAZGPP5SJpSF95lOl3-C u5Lvl4zPBDwdGgkpAdqgbMe0130 assertion
has provenance: NP55535.RAZGPP5SJpSF95lOl3-C u5Lvl4zPBDwdGgkpAdqgbMe0130 provenance
has publication info: NP55535.RAZGPP5SJpSF95lOl3-C u5Lvl4zPBDwdGgkpAdqgbMe0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55535.RAZGPP5SJpSF95lOl3-C u5Lvl4zPBDwdGgkpAdqgbMe0130 assertion
type: Assertion
description: [These results indicate that the gene encoding KLF7 is a novel candidate for conferring genetic susceptibility to type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15937668
was generated by: ECO_0000203

NP55537.RAQzq2pwq7g Hpjo3GdW wlHPKDDiKN2pLj1qIxVZc-4Q
has assertion: NP55537.RAQzq2pwq7g Hpjo3GdW wlHPKDDiKN2pLj1qIxVZc-4Q130 assertion
has provenance: NP55537.RAQzq2pwq7g Hpjo3GdW wlHPKDDiKN2pLj1qIxVZc-4Q130 provenance
has publication info: NP55537.RAQzq2pwq7g Hpjo3GdW wlHPKDDiKN2pLj1qIxVZc-4Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55537.RAQzq2pwq7g Hpjo3GdW wlHPKDDiKN2pLj1qIxVZc-4Q130 assertion
type: Assertion
description: [In this study, Southeast Asian AML patients with a favorable karyotype including t(8;21)/AML-ETO, inv(16)(CBF beta/SMMHC), and t(15;17)/PML-RAR alpha were genotyped for KIT and FLT3 RTK mutations by PCR and sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18977345
was generated by: ECO_0000203

NP55541.RAeka kIJNfnlRBMjWFnwp-grmowv9MKkZ8cgKcaAK0QA
has assertion: NP55541.RAeka kIJNfnlRBMjWFnwp-grmowv9MKkZ8cgKcaAK0QA130 assertion
has provenance: NP55541.RAeka kIJNfnlRBMjWFnwp-grmowv9MKkZ8cgKcaAK0QA130 provenance
has publication info: NP55541.RAeka kIJNfnlRBMjWFnwp-grmowv9MKkZ8cgKcaAK0QA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55541.RAeka kIJNfnlRBMjWFnwp-grmowv9MKkZ8cgKcaAK0QA130 assertion
type: Assertion
description: [Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16076867
was generated by: ECO_0000203

NP55547.RAfnT0uXglV3-Kq5-41YONrlOZKFFkXvyGS3p5jVyf sE
has assertion: NP55547.RAfnT0uXglV3-Kq5-41YONrlOZKFFkXvyGS3p5jVyf sE130 assertion
has provenance: NP55547.RAfnT0uXglV3-Kq5-41YONrlOZKFFkXvyGS3p5jVyf sE130 provenance
has publication info: NP55547.RAfnT0uXglV3-Kq5-41YONrlOZKFFkXvyGS3p5jVyf sE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55547.RAfnT0uXglV3-Kq5-41YONrlOZKFFkXvyGS3p5jVyf sE130 assertion
type: Assertion
description: [It was concluded that certain KIR genes and genotypes may associate with cervical neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15730517
was generated by: ECO_0000203

NP55552.RAbTpapTt2-SgXxbgwR2Pph7w0JLlAXkpoaT1dJ dlSU
has assertion: NP55552.RAbTpapTt2-SgXxbgwR2Pph7w0JLlAXkpoaT1dJ dlSU130 assertion
has provenance: NP55552.RAbTpapTt2-SgXxbgwR2Pph7w0JLlAXkpoaT1dJ dlSU130 provenance
has publication info: NP55552.RAbTpapTt2-SgXxbgwR2Pph7w0JLlAXkpoaT1dJ dlSU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55552.RAbTpapTt2-SgXxbgwR2Pph7w0JLlAXkpoaT1dJ dlSU130 assertion
type: Assertion
description: [It was concluded that certain KIR genes and genotypes may associate with cervical neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15730517
was generated by: ECO_0000203

NP55554.RAScf3bGFnYCGzS6 yCpZHomKwYekB7VlsO7jQfGnNilM
has assertion: NP55554.RAScf3bGFnYCGzS6 yCpZHomKwYekB7VlsO7jQfGnNilM130 assertion
has provenance: NP55554.RAScf3bGFnYCGzS6 yCpZHomKwYekB7VlsO7jQfGnNilM130 provenance
has publication info: NP55554.RAScf3bGFnYCGzS6 yCpZHomKwYekB7VlsO7jQfGnNilM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55554.RAScf3bGFnYCGzS6 yCpZHomKwYekB7VlsO7jQfGnNilM130 assertion
type: Assertion
description: [A study of the killer cell immunoglobulin-like receptor gene KIR2DS1 in a Caucasoid Brazilian population with psoriasis vulgaris.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18643961
was generated by: ECO_0000203

NP55557.RAQb10MOtDqiGreCCI2wI4CsiT479tBN 5Fgm5vYKevSI
has assertion: NP55557.RAQb10MOtDqiGreCCI2wI4CsiT479tBN 5Fgm5vYKevSI130 assertion
has provenance: NP55557.RAQb10MOtDqiGreCCI2wI4CsiT479tBN 5Fgm5vYKevSI130 provenance
has publication info: NP55557.RAQb10MOtDqiGreCCI2wI4CsiT479tBN 5Fgm5vYKevSI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55557.RAQb10MOtDqiGreCCI2wI4CsiT479tBN 5Fgm5vYKevSI130 assertion
type: Assertion
description: [This result strongly speaks for a role of KIR2DS1 on recognition of HLA-Cw6 in susceptibility to psoriasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15310528
was generated by: ECO_0000203

NP55558.RAR8Zj-wc7YYHKkzz-ulZXH8RfWyrXvra5WXEVxN23MWQ
has assertion: NP55558.RAR8Zj-wc7YYHKkzz-ulZXH8RfWyrXvra5WXEVxN23MWQ130 assertion
has provenance: NP55558.RAR8Zj-wc7YYHKkzz-ulZXH8RfWyrXvra5WXEVxN23MWQ130 provenance
has publication info: NP55558.RAR8Zj-wc7YYHKkzz-ulZXH8RfWyrXvra5WXEVxN23MWQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55558.RAR8Zj-wc7YYHKkzz-ulZXH8RfWyrXvra5WXEVxN23MWQ130 assertion
type: Assertion
description: [The developed application can estimate haplotype frequencies for every type of polymorphism and can effectively be used in genetic research as illustrated by a novel finding regarding the genetic susceptibility to psoriasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18681957
was generated by: ECO_0000203

NP55559.RAadMAo41UQ53C7avPK ROVp6d0AizW8qxttrT R5-wqA
has assertion: NP55559.RAadMAo41UQ53C7avPK ROVp6d0AizW8qxttrT R5-wqA130 assertion
has provenance: NP55559.RAadMAo41UQ53C7avPK ROVp6d0AizW8qxttrT R5-wqA130 provenance
has publication info: NP55559.RAadMAo41UQ53C7avPK ROVp6d0AizW8qxttrT R5-wqA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55559.RAadMAo41UQ53C7avPK ROVp6d0AizW8qxttrT R5-wqA130 assertion
type: Assertion
description: [A study of the killer cell immunoglobulin-like receptor gene KIR2DS1 in a Caucasoid Brazilian population with psoriasis vulgaris.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18643961
was generated by: ECO_0000203

NP55560.RARv6BS-sOu0FpgrglmnuTc 4fGKvCYzqT74yNd5bhvVM
has assertion: NP55560.RARv6BS-sOu0FpgrglmnuTc 4fGKvCYzqT74yNd5bhvVM130 assertion
has provenance: NP55560.RARv6BS-sOu0FpgrglmnuTc 4fGKvCYzqT74yNd5bhvVM130 provenance
has publication info: NP55560.RARv6BS-sOu0FpgrglmnuTc 4fGKvCYzqT74yNd5bhvVM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55560.RARv6BS-sOu0FpgrglmnuTc 4fGKvCYzqT74yNd5bhvVM130 assertion
type: Assertion
description: [The data obtained in this study imply that there may not be a direct association between KIR gene content in the genome and the presence of malignant melanoma, or melanoma progression. However, some HLA haplotypes could be predisposing to MM in the Bulgarian population. Furthermore, distinct KIR/HLA ligand combinations may be relevant to the development of malignancy whereby inhibition overrides activation of NK cells and T cells expressing NK-associated receptors, which in turn might facilitate tumor escape and progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15248031
was generated by: ECO_0000203

NP55564.RATEHSigYvF 5OnY5ymGgZ8yRhq3vnyyW1icwRScOVdZ4
has assertion: NP55564.RATEHSigYvF 5OnY5ymGgZ8yRhq3vnyyW1icwRScOVdZ4130 assertion
has provenance: NP55564.RATEHSigYvF 5OnY5ymGgZ8yRhq3vnyyW1icwRScOVdZ4130 provenance
has publication info: NP55564.RATEHSigYvF 5OnY5ymGgZ8yRhq3vnyyW1icwRScOVdZ4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55564.RATEHSigYvF 5OnY5ymGgZ8yRhq3vnyyW1icwRScOVdZ4130 assertion
type: Assertion
description: [Activating killer cell immunoglobulin-like receptor gene KIR2DS1 is associated with psoriatic arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16112031
was generated by: ECO_0000203

NP55565.RAWSeeqxfViGlH3bYtx2WRsBfUtvanjN5MAdasaBprY64
has assertion: NP55565.RAWSeeqxfViGlH3bYtx2WRsBfUtvanjN5MAdasaBprY64130 assertion
has provenance: NP55565.RAWSeeqxfViGlH3bYtx2WRsBfUtvanjN5MAdasaBprY64130 provenance
has publication info: NP55565.RAWSeeqxfViGlH3bYtx2WRsBfUtvanjN5MAdasaBprY64130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55565.RAWSeeqxfViGlH3bYtx2WRsBfUtvanjN5MAdasaBprY64130 assertion
type: Assertion
description: [These results provide strong evidence for pathogenic variant(s) in the 276-kb region harboring IDE that influence intermediate AD phenotypes and risk for AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15024728
was generated by: ECO_0000203

NP55571.RAexW1C9BsrNEn2jRFSjOe WUZ050F4Fq8-exS08Te2do
has assertion: NP55571.RAexW1C9BsrNEn2jRFSjOe WUZ050F4Fq8-exS08Te2do130 assertion
has provenance: NP55571.RAexW1C9BsrNEn2jRFSjOe WUZ050F4Fq8-exS08Te2do130 provenance
has publication info: NP55571.RAexW1C9BsrNEn2jRFSjOe WUZ050F4Fq8-exS08Te2do130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55571.RAexW1C9BsrNEn2jRFSjOe WUZ050F4Fq8-exS08Te2do130 assertion
type: Assertion
description: [Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17033633
was generated by: ECO_0000203

NP55573.RAWGvZJKrgDY-4x9LEy745RuRG48j4VoEiN0x12p5Pxlw
has assertion: NP55573.RAWGvZJKrgDY-4x9LEy745RuRG48j4VoEiN0x12p5Pxlw130 assertion
has provenance: NP55573.RAWGvZJKrgDY-4x9LEy745RuRG48j4VoEiN0x12p5Pxlw130 provenance
has publication info: NP55573.RAWGvZJKrgDY-4x9LEy745RuRG48j4VoEiN0x12p5Pxlw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55573.RAWGvZJKrgDY-4x9LEy745RuRG48j4VoEiN0x12p5Pxlw130 assertion
type: Assertion
description: [A common variant associated with dyslexia reduces expression of the KIAA0319 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19325871
was generated by: ECO_0000203

NP55575.RAYbSjrRQrrab79i80FcppEp-IdjqXlPzaGfOsF8 em5c
has assertion: NP55575.RAYbSjrRQrrab79i80FcppEp-IdjqXlPzaGfOsF8 em5c130 assertion
has provenance: NP55575.RAYbSjrRQrrab79i80FcppEp-IdjqXlPzaGfOsF8 em5c130 provenance
has publication info: NP55575.RAYbSjrRQrrab79i80FcppEp-IdjqXlPzaGfOsF8 em5c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55575.RAYbSjrRQrrab79i80FcppEp-IdjqXlPzaGfOsF8 em5c130 assertion
type: Assertion
description: [We analyzed the genetic polymorphisms of vascular endothelial growth factor (VEGF) and its receptors Fms-related tyrosine kinase-1, kinase insert domain receptor (KDR) in Japanese patients with Kawasaki disease (KD) and normal control subjects to examine whether these genes would contribute to the KD occurrence and/or the development of coronary artery lesion (CAL) in KD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15470196
was generated by: ECO_0000203

NP55577.RAdLh EEuuUaejRXcIazhfpohKxJO8vhzou4jGJcCq5Ds
has assertion: NP55577.RAdLh EEuuUaejRXcIazhfpohKxJO8vhzou4jGJcCq5Ds130 assertion
has provenance: NP55577.RAdLh EEuuUaejRXcIazhfpohKxJO8vhzou4jGJcCq5Ds130 provenance
has publication info: NP55577.RAdLh EEuuUaejRXcIazhfpohKxJO8vhzou4jGJcCq5Ds130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55577.RAdLh EEuuUaejRXcIazhfpohKxJO8vhzou4jGJcCq5Ds130 assertion
type: Assertion
description: [We have tested the association between JME phenotype and an intragenic marker in KCNQ3 by using the transmission disequilibrium test in 119 probands and their parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12928862
was generated by: ECO_0000203

NP55581.RAUKwEigVg9-HM3CItraS2O9IQnhlgKG-E0HXKG3wDwjY
has assertion: NP55581.RAUKwEigVg9-HM3CItraS2O9IQnhlgKG-E0HXKG3wDwjY130 assertion
has provenance: NP55581.RAUKwEigVg9-HM3CItraS2O9IQnhlgKG-E0HXKG3wDwjY130 provenance
has publication info: NP55581.RAUKwEigVg9-HM3CItraS2O9IQnhlgKG-E0HXKG3wDwjY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55581.RAUKwEigVg9-HM3CItraS2O9IQnhlgKG-E0HXKG3wDwjY130 assertion
type: Assertion
description: [Association analysis of CAG repeats at the KCNN3 locus in Indian patients with bipolar disorder and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11121173
was generated by: ECO_0000203

NP55591.RAQuXFp-IVjmKt0jNeV8eXhlgi3acYYJEBFqgmAwfrNbE
has assertion: NP55591.RAQuXFp-IVjmKt0jNeV8eXhlgi3acYYJEBFqgmAwfrNbE130 assertion
has provenance: NP55591.RAQuXFp-IVjmKt0jNeV8eXhlgi3acYYJEBFqgmAwfrNbE130 provenance
has publication info: NP55591.RAQuXFp-IVjmKt0jNeV8eXhlgi3acYYJEBFqgmAwfrNbE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55591.RAQuXFp-IVjmKt0jNeV8eXhlgi3acYYJEBFqgmAwfrNbE130 assertion
type: Assertion
description: [ The significance of the G(-930)A polymorphism of CYBA was confirmed in the present study with adequate statistical power, which strengthens the hypothesis that this polymorphism is important in the pathogenesis of hypertension and confers susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15671602
was generated by: ECO_0000203

NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE
has assertion: NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130 assertion
has provenance: NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130 provenance
has publication info: NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55592.RAf87gYuWj1l1EH021d6f6SXBK-ALSrZtptFT8QgWnvfE130 assertion
type: Assertion
description: [The overall results supported that the genetic variants in the contractile pathway of VSMC could contribute to hypertension risk independently or in an interactive manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18496125
was generated by: ECO_0000203

NP55598.RAQcILeMC63VGqeDmXYt2OFBMsKuLPlB7ouDMBVDfhoa0
has assertion: NP55598.RAQcILeMC63VGqeDmXYt2OFBMsKuLPlB7ouDMBVDfhoa0130 assertion
has provenance: NP55598.RAQcILeMC63VGqeDmXYt2OFBMsKuLPlB7ouDMBVDfhoa0130 provenance
has publication info: NP55598.RAQcILeMC63VGqeDmXYt2OFBMsKuLPlB7ouDMBVDfhoa0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55598.RAQcILeMC63VGqeDmXYt2OFBMsKuLPlB7ouDMBVDfhoa0130 assertion
type: Assertion
description: [No significant association of PPARG, PGC1, IRS1, KCNJ11 and TCF7L2 gene polymorphisms and the age at diagnosis of T2DM was observed in the present study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20437825
was generated by: ECO_0000203

NP55601.RAbORFP7LWnahoYv9nCoPxcys lFs6KXYTBxcnogZYCMY
has assertion: NP55601.RAbORFP7LWnahoYv9nCoPxcys lFs6KXYTBxcnogZYCMY130 assertion
has provenance: NP55601.RAbORFP7LWnahoYv9nCoPxcys lFs6KXYTBxcnogZYCMY130 provenance
has publication info: NP55601.RAbORFP7LWnahoYv9nCoPxcys lFs6KXYTBxcnogZYCMY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55601.RAbORFP7LWnahoYv9nCoPxcys lFs6KXYTBxcnogZYCMY130 assertion
type: Assertion
description: [We investigated the effects of the E23K variant of KCNJ11 (potassium inwardly-rectifying channel, subfamily J, member 11) on risk for SH in patients with type 2 diabetes (T2D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19214942
was generated by: ECO_0000203

NP55608.RAQKnUWISNZQ2SmvjVa-yPvINzTejWp gWV4tkQjUJVFc
has assertion: NP55608.RAQKnUWISNZQ2SmvjVa-yPvINzTejWp gWV4tkQjUJVFc130 assertion
has provenance: NP55608.RAQKnUWISNZQ2SmvjVa-yPvINzTejWp gWV4tkQjUJVFc130 provenance
has publication info: NP55608.RAQKnUWISNZQ2SmvjVa-yPvINzTejWp gWV4tkQjUJVFc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55608.RAQKnUWISNZQ2SmvjVa-yPvINzTejWp gWV4tkQjUJVFc130 assertion
type: Assertion
description: [We have investigated three such genes, KCNJ3, KCNJ6 and KCNQ2, by association studies using a broad sample of idiopathic generalised epilepsy (IGE) unselected by syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12458027
was generated by: ECO_0000203

NP55610.RAcbY-dCAQwyjYp4G2XHlzV5z5gLdZ ChF8l-nj qMT2s
has assertion: NP55610.RAcbY-dCAQwyjYp4G2XHlzV5z5gLdZ ChF8l-nj qMT2s130 assertion
has provenance: NP55610.RAcbY-dCAQwyjYp4G2XHlzV5z5gLdZ ChF8l-nj qMT2s130 provenance
has publication info: NP55610.RAcbY-dCAQwyjYp4G2XHlzV5z5gLdZ ChF8l-nj qMT2s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55610.RAcbY-dCAQwyjYp4G2XHlzV5z5gLdZ ChF8l-nj qMT2s130 assertion
type: Assertion
description: [The prevalent Glu23Lys polymorphism in the potassium inward rectifier 6.2 (KIR6.2) gene is associated with impaired glucagon suppression in response to hyperglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12196481
was generated by: ECO_0000203

NP55613.RAaD57eyJ70CzJBY6nFeKPt4YcK0hxJx3QvNQSbd-9M1Q
has assertion: NP55613.RAaD57eyJ70CzJBY6nFeKPt4YcK0hxJx3QvNQSbd-9M1Q130 assertion
has provenance: NP55613.RAaD57eyJ70CzJBY6nFeKPt4YcK0hxJx3QvNQSbd-9M1Q130 provenance
has publication info: NP55613.RAaD57eyJ70CzJBY6nFeKPt4YcK0hxJx3QvNQSbd-9M1Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55613.RAaD57eyJ70CzJBY6nFeKPt4YcK0hxJx3QvNQSbd-9M1Q130 assertion
type: Assertion
description: [These differences can help to identify LQTS patients and distinguish LQT1 from LQT2 genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20226272
was generated by: ECO_0000203

NP55615.RAckR BwQ84EkUGO4thoiAxIY-szE66ZamMx3lh42EVHc
has assertion: NP55615.RAckR BwQ84EkUGO4thoiAxIY-szE66ZamMx3lh42EVHc130 assertion
has provenance: NP55615.RAckR BwQ84EkUGO4thoiAxIY-szE66ZamMx3lh42EVHc130 provenance
has publication info: NP55615.RAckR BwQ84EkUGO4thoiAxIY-szE66ZamMx3lh42EVHc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55615.RAckR BwQ84EkUGO4thoiAxIY-szE66ZamMx3lh42EVHc130 assertion
type: Assertion
description: [The SALSA multiplex ligation-dependent probe amplification LQTS kit from MRC-Holland was used to analyze the 3 major LQTS-associated genes, KCNQ1, KCNH2, and SCN5A, and the 2 minor genes, KCNE1 and KCNE2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20920651
was generated by: ECO_0000203

NP55616.RASbJUW7f8r6Q83OxFiDtUHq6tP5ZGt3XeJ39mcFwDePc
has assertion: NP55616.RASbJUW7f8r6Q83OxFiDtUHq6tP5ZGt3XeJ39mcFwDePc130 assertion
has provenance: NP55616.RASbJUW7f8r6Q83OxFiDtUHq6tP5ZGt3XeJ39mcFwDePc130 provenance
has publication info: NP55616.RASbJUW7f8r6Q83OxFiDtUHq6tP5ZGt3XeJ39mcFwDePc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55616.RASbJUW7f8r6Q83OxFiDtUHq6tP5ZGt3XeJ39mcFwDePc130 assertion
type: Assertion
description: [Retrospective analysis of the first 2,500 cases (1,515 female patients, average age at testing 23 +/- 17 years, range 0 to 90 years) scanned for mutations in 5 of the LQTS-susceptibility genes: KCNQ1 (LQT1), KCNH2 (LQT2), SCN5A (LQT3), KCNE1 (LQT5), and KCNE2 (LQT6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19716085
was generated by: ECO_0000203

NP55625.RAW0B jc4WAl5g853rAD1-7oOl R19lMXym1 CHnBAUyA
has assertion: NP55625.RAW0B jc4WAl5g853rAD1-7oOl R19lMXym1 CHnBAUyA130 assertion
has provenance: NP55625.RAW0B jc4WAl5g853rAD1-7oOl R19lMXym1 CHnBAUyA130 provenance
has publication info: NP55625.RAW0B jc4WAl5g853rAD1-7oOl R19lMXym1 CHnBAUyA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55625.RAW0B jc4WAl5g853rAD1-7oOl R19lMXym1 CHnBAUyA130 assertion
type: Assertion
description: [The results of this study suggest that a missense mutation in KCNE5 may be associated with nonfamilial or acquired forms of AF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18313602
was generated by: ECO_0000203

NP55628.RAWArHOu9eBsFYBlD wwle0MNSFjLR8NBAVqSNW06OAfI
has assertion: NP55628.RAWArHOu9eBsFYBlD wwle0MNSFjLR8NBAVqSNW06OAfI130 assertion
has provenance: NP55628.RAWArHOu9eBsFYBlD wwle0MNSFjLR8NBAVqSNW06OAfI130 provenance
has publication info: NP55628.RAWArHOu9eBsFYBlD wwle0MNSFjLR8NBAVqSNW06OAfI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55628.RAWArHOu9eBsFYBlD wwle0MNSFjLR8NBAVqSNW06OAfI130 assertion
type: Assertion
description: [Our results suggest that in patients without RUNX1 mutation, several other molecular aberrations, separately or in combination, contribute to a common minimally differentiated phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19773259
was generated by: ECO_0000203

NP55629.RAbNPmXipWVavLjbubGSJ0cwIV1MMmI4KVH1niRk4mky8
has assertion: NP55629.RAbNPmXipWVavLjbubGSJ0cwIV1MMmI4KVH1niRk4mky8130 assertion
has provenance: NP55629.RAbNPmXipWVavLjbubGSJ0cwIV1MMmI4KVH1niRk4mky8130 provenance
has publication info: NP55629.RAbNPmXipWVavLjbubGSJ0cwIV1MMmI4KVH1niRk4mky8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55629.RAbNPmXipWVavLjbubGSJ0cwIV1MMmI4KVH1niRk4mky8130 assertion
type: Assertion
description: [The associations of Janus kinase-2 (JAK2) A830G polymorphism and the treatment outcomes in patients with acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20536350
was generated by: ECO_0000203

NP55633.RASwW2O283nszV9O9aI9Hz506Ib1uz11ilu-8bAM-QBpc
has assertion: NP55633.RASwW2O283nszV9O9aI9Hz506Ib1uz11ilu-8bAM-QBpc130 assertion
has provenance: NP55633.RASwW2O283nszV9O9aI9Hz506Ib1uz11ilu-8bAM-QBpc130 provenance
has publication info: NP55633.RASwW2O283nszV9O9aI9Hz506Ib1uz11ilu-8bAM-QBpc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55633.RASwW2O283nszV9O9aI9Hz506Ib1uz11ilu-8bAM-QBpc130 assertion
type: Assertion
description: [JAK2 germline genetic variation affects disease susceptibility in primary myelofibrosis regardless of V617F mutational status: nullizygosity for the JAK2 46/1 haplotype is associated with inferior survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19847199
was generated by: ECO_0000203

NP55635.RARD 4DtpFJiycbIV Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc
has assertion: NP55635.RARD 4DtpFJiycbIV Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130 assertion
has provenance: NP55635.RARD 4DtpFJiycbIV Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130 provenance
has publication info: NP55635.RARD 4DtpFJiycbIV Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55635.RARD 4DtpFJiycbIV Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130 assertion
type: Assertion
description: [These data indicate that loss of wild-type clones at the progenitor level is a feature of MF (primary MF, post-ET MF, and post-PV MF), presumably due to expansion of the JAK2 V617F clone and that this characteristic is surprisingly independent of JAK2 V617F homozygosity, suggesting that additional genomic lesions may contribute to this unique molecular process that distinguishes MF from ET and PV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20888389
was generated by: ECO_0000203

NP55638.RAQ iO5ktgA hS8hchjGiXDs9-MTM8v0PomyvmBLjv2Y
has assertion: NP55638.RAQ iO5ktgA hS8hchjGiXDs9-MTM8v0PomyvmBLjv2Y130 assertion
has provenance: NP55638.RAQ iO5ktgA hS8hchjGiXDs9-MTM8v0PomyvmBLjv2Y130 provenance
has publication info: NP55638.RAQ iO5ktgA hS8hchjGiXDs9-MTM8v0PomyvmBLjv2Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55638.RAQ iO5ktgA hS8hchjGiXDs9-MTM8v0PomyvmBLjv2Y130 assertion
type: Assertion
description: [A diagnosis of polycythemia vera was confirmed in 53% of 62 participants using WHO criteria, which includes JAK2 617V>F testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19190168
was generated by: ECO_0000203

NP55640.RAUquPWZQZs3vT4Kigt08ei-GaU2pI5JEZo2aAEstIuoE
has assertion: NP55640.RAUquPWZQZs3vT4Kigt08ei-GaU2pI5JEZo2aAEstIuoE130 assertion
has provenance: NP55640.RAUquPWZQZs3vT4Kigt08ei-GaU2pI5JEZo2aAEstIuoE130 provenance
has publication info: NP55640.RAUquPWZQZs3vT4Kigt08ei-GaU2pI5JEZo2aAEstIuoE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55640.RAUquPWZQZs3vT4Kigt08ei-GaU2pI5JEZo2aAEstIuoE130 assertion
type: Assertion
description: [High percentage of JAK2 exon 12 mutation in Asian patients with polycythemia vera.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20660330
was generated by: ECO_0000203

NP55641.RASDs3 ep8JAmWLE8EF2z-qiyTHzIz714zmry KeFbRg4
has assertion: NP55641.RASDs3 ep8JAmWLE8EF2z-qiyTHzIz714zmry KeFbRg4130 assertion
has provenance: NP55641.RASDs3 ep8JAmWLE8EF2z-qiyTHzIz714zmry KeFbRg4130 provenance
has publication info: NP55641.RASDs3 ep8JAmWLE8EF2z-qiyTHzIz714zmry KeFbRg4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55641.RASDs3 ep8JAmWLE8EF2z-qiyTHzIz714zmry KeFbRg4130 assertion
type: Assertion
description: [JAK2 exon 12 mutation in JAK2V617F-negative polycythemia vera.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18297539
was generated by: ECO_0000203

NP55649.RAeCoRYp3 Mb5oTm9qNr1kL6G-llj9vDSc5rwH00IOpx4
has assertion: NP55649.RAeCoRYp3 Mb5oTm9qNr1kL6G-llj9vDSc5rwH00IOpx4130 assertion
has provenance: NP55649.RAeCoRYp3 Mb5oTm9qNr1kL6G-llj9vDSc5rwH00IOpx4130 provenance
has publication info: NP55649.RAeCoRYp3 Mb5oTm9qNr1kL6G-llj9vDSc5rwH00IOpx4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55649.RAeCoRYp3 Mb5oTm9qNr1kL6G-llj9vDSc5rwH00IOpx4130 assertion
type: Assertion
description: [Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12082592
was generated by: ECO_0000203

NP55652.RAZu6fVGWbWXy4cSjX30kaSM4XDAOIiNDqQefbLp9yoYE
has assertion: NP55652.RAZu6fVGWbWXy4cSjX30kaSM4XDAOIiNDqQefbLp9yoYE130 assertion
has provenance: NP55652.RAZu6fVGWbWXy4cSjX30kaSM4XDAOIiNDqQefbLp9yoYE130 provenance
has publication info: NP55652.RAZu6fVGWbWXy4cSjX30kaSM4XDAOIiNDqQefbLp9yoYE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55652.RAZu6fVGWbWXy4cSjX30kaSM4XDAOIiNDqQefbLp9yoYE130 assertion
type: Assertion
description: [The significant associations between certain gene variants with concentration variations in serum C-reactive protein and homocysteine among adult women need to be confirmed in further genetic association studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20078877
was generated by: ECO_0000203

NP55661.RASd4C6rCeLtrLfD4wpA Pt 4fMGQVeIOnsphh0JWzTU8
has assertion: NP55661.RASd4C6rCeLtrLfD4wpA Pt 4fMGQVeIOnsphh0JWzTU8130 assertion
has provenance: NP55661.RASd4C6rCeLtrLfD4wpA Pt 4fMGQVeIOnsphh0JWzTU8130 provenance
has publication info: NP55661.RASd4C6rCeLtrLfD4wpA Pt 4fMGQVeIOnsphh0JWzTU8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55661.RASd4C6rCeLtrLfD4wpA Pt 4fMGQVeIOnsphh0JWzTU8130 assertion
type: Assertion
description: [ Our results suggest, that the Pl(A1/A1) genotype of Pl(A) GPIIIa polymorphism is associated with more severe CAD in male Caucasian patients from the north region of Poland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12714203
was generated by: ECO_0000203

NP55662.RAY9UchNOy6pqSRETQQTEEKvR7gtdK-bqdaKGYlYNxuiw
has assertion: NP55662.RAY9UchNOy6pqSRETQQTEEKvR7gtdK-bqdaKGYlYNxuiw130 assertion
has provenance: NP55662.RAY9UchNOy6pqSRETQQTEEKvR7gtdK-bqdaKGYlYNxuiw130 provenance
has publication info: NP55662.RAY9UchNOy6pqSRETQQTEEKvR7gtdK-bqdaKGYlYNxuiw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55662.RAY9UchNOy6pqSRETQQTEEKvR7gtdK-bqdaKGYlYNxuiw130 assertion
type: Assertion
description: [The findings of this study suggest that Pl(A1/A1) homozygotes may be prone to early atherosclerosis and more rapid progression of stable CAD whereas carriers of the Pl(A2) allele are more prone to thrombotic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11257275
was generated by: ECO_0000203

NP55663.RAXD-mRIMl9rE5olI8WXjXVm dSK XOVZaA1wffbjgynY
has assertion: NP55663.RAXD-mRIMl9rE5olI8WXjXVm dSK XOVZaA1wffbjgynY130 assertion
has provenance: NP55663.RAXD-mRIMl9rE5olI8WXjXVm dSK XOVZaA1wffbjgynY130 provenance
has publication info: NP55663.RAXD-mRIMl9rE5olI8WXjXVm dSK XOVZaA1wffbjgynY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55663.RAXD-mRIMl9rE5olI8WXjXVm dSK XOVZaA1wffbjgynY130 assertion
type: Assertion
description: [AR appears to be unrelated to differences in platelet COX-1 and COX-2 expression or to a novel platelet COX-1 SNP and the PlA(1)/A(2) SNP. However, a correlation exists to elevated eicosanoids generated by oxidative stress indicating COX-1-independent pathways for the generation of platelet activating molecules represent a potential cause for AR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16702043
was generated by: ECO_0000203

NP55668.RAcmCOSkr 9bfrnwwNu69tX2CDSuYkuYHQsVyQhFNr1QY
has assertion: NP55668.RAcmCOSkr 9bfrnwwNu69tX2CDSuYkuYHQsVyQhFNr1QY130 assertion
has provenance: NP55668.RAcmCOSkr 9bfrnwwNu69tX2CDSuYkuYHQsVyQhFNr1QY130 provenance
has publication info: NP55668.RAcmCOSkr 9bfrnwwNu69tX2CDSuYkuYHQsVyQhFNr1QY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55668.RAcmCOSkr 9bfrnwwNu69tX2CDSuYkuYHQsVyQhFNr1QY130 assertion
type: Assertion
description: [Human platelet alloantigens HPA-1, HPA-2, and HPA-3 polymorphisms associated with extent of severe coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19562259
was generated by: ECO_0000203

NP55675.RATeFlxA6ea4LiANMPi6It5jcN-2T90ibX8dj0ef8h0fY
has assertion: NP55675.RATeFlxA6ea4LiANMPi6It5jcN-2T90ibX8dj0ef8h0fY130 assertion
has provenance: NP55675.RATeFlxA6ea4LiANMPi6It5jcN-2T90ibX8dj0ef8h0fY130 provenance
has publication info: NP55675.RATeFlxA6ea4LiANMPi6It5jcN-2T90ibX8dj0ef8h0fY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55675.RATeFlxA6ea4LiANMPi6It5jcN-2T90ibX8dj0ef8h0fY130 assertion
type: Assertion
description: [ In patients with FHC polymorphisms in factor VII and GPIIIa genes but not C677T polymorphism of MTHFR gene were associated with the presence of IHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16091654
was generated by: ECO_0000203

NP55677.RAQjca1xu6bGq1 T1j7E4clQMUEiWXHsqM vZC8RsCebo
has assertion: NP55677.RAQjca1xu6bGq1 T1j7E4clQMUEiWXHsqM vZC8RsCebo130 assertion
has provenance: NP55677.RAQjca1xu6bGq1 T1j7E4clQMUEiWXHsqM vZC8RsCebo130 provenance
has publication info: NP55677.RAQjca1xu6bGq1 T1j7E4clQMUEiWXHsqM vZC8RsCebo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55677.RAQjca1xu6bGq1 T1j7E4clQMUEiWXHsqM vZC8RsCebo130 assertion
type: Assertion
description: [We have studied structure of polymorphisms of genes of blood clotting factors II, V, VII, platelet membrane glycoprotein IIIa (GPIIIa) and enzyme methylenetetrahydrofolate reductase (MTHFR) in patients with ischemic heart disease (IHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19463111
was generated by: ECO_0000203

NP55681.RAamGYRlvSRJHxW4dsOaGYIy3cmpNJDlokOVcBLlNkBUE
has assertion: NP55681.RAamGYRlvSRJHxW4dsOaGYIy3cmpNJDlokOVcBLlNkBUE130 assertion
has provenance: NP55681.RAamGYRlvSRJHxW4dsOaGYIy3cmpNJDlokOVcBLlNkBUE130 provenance
has publication info: NP55681.RAamGYRlvSRJHxW4dsOaGYIy3cmpNJDlokOVcBLlNkBUE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55681.RAamGYRlvSRJHxW4dsOaGYIy3cmpNJDlokOVcBLlNkBUE130 assertion
type: Assertion
description: [Our data suggest that the Pl(A2) polymorphism is a genetic determinant of ischemic stroke in a selected high-risk hypertensive population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17278970
was generated by: ECO_0000203

NP55695.RAWuyiA0EAugWFSAnr-D43 cMymunMxsnCWTPcV38aP80
has assertion: NP55695.RAWuyiA0EAugWFSAnr-D43 cMymunMxsnCWTPcV38aP80130 assertion
has provenance: NP55695.RAWuyiA0EAugWFSAnr-D43 cMymunMxsnCWTPcV38aP80130 provenance
has publication info: NP55695.RAWuyiA0EAugWFSAnr-D43 cMymunMxsnCWTPcV38aP80130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55695.RAWuyiA0EAugWFSAnr-D43 cMymunMxsnCWTPcV38aP80130 assertion
type: Assertion
description: [Our data suggest that inheritance of the integrin beta(3) Leu33Pro polymorphism may increase the breast cancer risk by age 45 in the German population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15609125
was generated by: ECO_0000203

NP55697.RAYv7AaVc V i3ajF19etFeH1kE 0Dah51grj 30UC3sM
has assertion: NP55697.RAYv7AaVc V i3ajF19etFeH1kE 0Dah51grj 30UC3sM130 assertion
has provenance: NP55697.RAYv7AaVc V i3ajF19etFeH1kE 0Dah51grj 30UC3sM130 provenance
has publication info: NP55697.RAYv7AaVc V i3ajF19etFeH1kE 0Dah51grj 30UC3sM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55697.RAYv7AaVc V i3ajF19etFeH1kE 0Dah51grj 30UC3sM130 assertion
type: Assertion
description: [Do BRCA1 modifiers also affect the risk of breast cancer in non-carriers?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19071013
was generated by: ECO_0000203

NP55698.RAdkrs2PBAL8WZ1BGoBgCTp5mV6YyVn6WQ2niRuMnHrVw
has assertion: NP55698.RAdkrs2PBAL8WZ1BGoBgCTp5mV6YyVn6WQ2niRuMnHrVw130 assertion
has provenance: NP55698.RAdkrs2PBAL8WZ1BGoBgCTp5mV6YyVn6WQ2niRuMnHrVw130 provenance
has publication info: NP55698.RAdkrs2PBAL8WZ1BGoBgCTp5mV6YyVn6WQ2niRuMnHrVw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55698.RAdkrs2PBAL8WZ1BGoBgCTp5mV6YyVn6WQ2niRuMnHrVw130 assertion
type: Assertion
description: [Our data suggest that the FAS 1377G>A and IL10 592C>A polymorphisms could modify disease-free and overall survival in women with lymph node-positive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20204402
was generated by: ECO_0000203

NP55699.RAT4AghYCuRaRu8Lkrg5mHZiz6dIgpnupyZPJCkfOLzF8
has assertion: NP55699.RAT4AghYCuRaRu8Lkrg5mHZiz6dIgpnupyZPJCkfOLzF8130 assertion
has provenance: NP55699.RAT4AghYCuRaRu8Lkrg5mHZiz6dIgpnupyZPJCkfOLzF8130 provenance
has publication info: NP55699.RAT4AghYCuRaRu8Lkrg5mHZiz6dIgpnupyZPJCkfOLzF8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55699.RAT4AghYCuRaRu8Lkrg5mHZiz6dIgpnupyZPJCkfOLzF8130 assertion
type: Assertion
description: [ A novel Phe171Cys mutation in the alpha(IIb) gene of patients with GT is associated with abrogation of alpha(IIb)beta(3) complex formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15219201
was generated by: ECO_0000203

NP55707.RASCebukv26KZefxXZGwschz TJWApoYidGw9HYlzMoSA
has assertion: NP55707.RASCebukv26KZefxXZGwschz TJWApoYidGw9HYlzMoSA130 assertion
has provenance: NP55707.RASCebukv26KZefxXZGwschz TJWApoYidGw9HYlzMoSA130 provenance
has publication info: NP55707.RASCebukv26KZefxXZGwschz TJWApoYidGw9HYlzMoSA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55707.RASCebukv26KZefxXZGwschz TJWApoYidGw9HYlzMoSA130 assertion
type: Assertion
description: [ Individuals homozygous for the Leu33Pro polymorphism of the beta3 integrin subunit have an increased cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12902444
was generated by: ECO_0000203

NP55718.RAZLw5u-rsYxenTOTbgmVFsc5q6h32Ik5IG-7 mmohZL4
has assertion: NP55718.RAZLw5u-rsYxenTOTbgmVFsc5q6h32Ik5IG-7 mmohZL4130 assertion
has provenance: NP55718.RAZLw5u-rsYxenTOTbgmVFsc5q6h32Ik5IG-7 mmohZL4130 provenance
has publication info: NP55718.RAZLw5u-rsYxenTOTbgmVFsc5q6h32Ik5IG-7 mmohZL4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55718.RAZLw5u-rsYxenTOTbgmVFsc5q6h32Ik5IG-7 mmohZL4130 assertion
type: Assertion
description: [Molecular genetics of microvascular disease in diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12724690
was generated by: ECO_0000203

NP55722.RAbwvAnMDGXqWB0bs1t9EF4lhANM4bWvE8YY5MueaPcWM
has assertion: NP55722.RAbwvAnMDGXqWB0bs1t9EF4lhANM4bWvE8YY5MueaPcWM130 assertion
has provenance: NP55722.RAbwvAnMDGXqWB0bs1t9EF4lhANM4bWvE8YY5MueaPcWM130 provenance
has publication info: NP55722.RAbwvAnMDGXqWB0bs1t9EF4lhANM4bWvE8YY5MueaPcWM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55722.RAbwvAnMDGXqWB0bs1t9EF4lhANM4bWvE8YY5MueaPcWM130 assertion
type: Assertion
description: [We conclude that genetic variants in the CD11 cluster may play a role in the development of gastric ulcer in chronic H. pylori infection presumably by influencing leukocyte adhesion. The biological effect of genetic variants of CD11c in gastric inflammation needs further clarification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15730520
was generated by: ECO_0000203

NP55726.RAWVjRfg kTRjxASMkCRYlPoquptaGKnS0qH01lPBNpGo
has assertion: NP55726.RAWVjRfg kTRjxASMkCRYlPoquptaGKnS0qH01lPBNpGo130 assertion
has provenance: NP55726.RAWVjRfg kTRjxASMkCRYlPoquptaGKnS0qH01lPBNpGo130 provenance
has publication info: NP55726.RAWVjRfg kTRjxASMkCRYlPoquptaGKnS0qH01lPBNpGo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55726.RAWVjRfg kTRjxASMkCRYlPoquptaGKnS0qH01lPBNpGo130 assertion
type: Assertion
description: [Genetic polymorphisms of platelet adhesive molecules: association with breast cancer risk and clinical presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12908817
was generated by: ECO_0000203

NP55727.RAZF30Aq84-qooPLX7HBZynx7aE CPfNVu3LOIN8M2FgA
has assertion: NP55727.RAZF30Aq84-qooPLX7HBZynx7aE CPfNVu3LOIN8M2FgA130 assertion
has provenance: NP55727.RAZF30Aq84-qooPLX7HBZynx7aE CPfNVu3LOIN8M2FgA130 provenance
has publication info: NP55727.RAZF30Aq84-qooPLX7HBZynx7aE CPfNVu3LOIN8M2FgA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55727.RAZF30Aq84-qooPLX7HBZynx7aE CPfNVu3LOIN8M2FgA130 assertion
type: Assertion
description: [Polymorphisms in predicted microRNA-binding sites in integrin genes and breast cancer: ITGB4 as prognostic marker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18550570
was generated by: ECO_0000203

NP55730.RAV-C0-VL6kPZNYMvqZUWk59IRiDXogZD3uCXWy1zbEcY
has assertion: NP55730.RAV-C0-VL6kPZNYMvqZUWk59IRiDXogZD3uCXWy1zbEcY130 assertion
has provenance: NP55730.RAV-C0-VL6kPZNYMvqZUWk59IRiDXogZD3uCXWy1zbEcY130 provenance
has publication info: NP55730.RAV-C0-VL6kPZNYMvqZUWk59IRiDXogZD3uCXWy1zbEcY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55730.RAV-C0-VL6kPZNYMvqZUWk59IRiDXogZD3uCXWy1zbEcY130 assertion
type: Assertion
description: [Prevalence of genetic risk factors for coronary artery disease in Corsica island (France).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16248996
was generated by: ECO_0000203

NP55738.RASvNh-GnK-4BGwu cDxq63gzZKheFfS3NxD3E425Ssd4
has assertion: NP55738.RASvNh-GnK-4BGwu cDxq63gzZKheFfS3NxD3E425Ssd4130 assertion
has provenance: NP55738.RASvNh-GnK-4BGwu cDxq63gzZKheFfS3NxD3E425Ssd4130 provenance
has publication info: NP55738.RASvNh-GnK-4BGwu cDxq63gzZKheFfS3NxD3E425Ssd4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55738.RASvNh-GnK-4BGwu cDxq63gzZKheFfS3NxD3E425Ssd4130 assertion
type: Assertion
description: [ This study does not support the association between the PIA1/A2 polymorphism and cryptogenic stroke or TIA in patients aged 45 or less.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12586134
was generated by: ECO_0000203

NP55751.RAQ2fNo10kH3Fqv5iRYEEakP0qz87 BzQh8V HeI4EX-8
has assertion: NP55751.RAQ2fNo10kH3Fqv5iRYEEakP0qz87 BzQh8V HeI4EX-8130 assertion
has provenance: NP55751.RAQ2fNo10kH3Fqv5iRYEEakP0qz87 BzQh8V HeI4EX-8130 provenance
has publication info: NP55751.RAQ2fNo10kH3Fqv5iRYEEakP0qz87 BzQh8V HeI4EX-8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55751.RAQ2fNo10kH3Fqv5iRYEEakP0qz87 BzQh8V HeI4EX-8130 assertion
type: Assertion
description: [ The platelet glycoproteins polymorphisms studied are not an independent risk factor for AMI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12073410
was generated by: ECO_0000203

NP55756.RAUTQ JqTU4eHUqnPmClFkHX1IjuywuNSHgoO-UUnttgs
has assertion: NP55756.RAUTQ JqTU4eHUqnPmClFkHX1IjuywuNSHgoO-UUnttgs130 assertion
has provenance: NP55756.RAUTQ JqTU4eHUqnPmClFkHX1IjuywuNSHgoO-UUnttgs130 provenance
has publication info: NP55756.RAUTQ JqTU4eHUqnPmClFkHX1IjuywuNSHgoO-UUnttgs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55756.RAUTQ JqTU4eHUqnPmClFkHX1IjuywuNSHgoO-UUnttgs130 assertion
type: Assertion
description: [Genetic polymorphism C807T increases the risk for premature MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16697311
was generated by: ECO_0000203

NP55761.RATQATTZMSh3X1jWmgvSPwxrUULXdNeA0qIa2NEm9G6xs
has assertion: NP55761.RATQATTZMSh3X1jWmgvSPwxrUULXdNeA0qIa2NEm9G6xs130 assertion
has provenance: NP55761.RATQATTZMSh3X1jWmgvSPwxrUULXdNeA0qIa2NEm9G6xs130 provenance
has publication info: NP55761.RATQATTZMSh3X1jWmgvSPwxrUULXdNeA0qIa2NEm9G6xs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55761.RATQATTZMSh3X1jWmgvSPwxrUULXdNeA0qIa2NEm9G6xs130 assertion
type: Assertion
description: [ Our results suggest that these polymorphisms play a minor role in PIH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12499711
was generated by: ECO_0000203

NP55764.RAbWB04evUnvaVZZY1am98xSX0bLNPzZZYGgmZMSemaDw
has assertion: NP55764.RAbWB04evUnvaVZZY1am98xSX0bLNPzZZYGgmZMSemaDw130 assertion
has provenance: NP55764.RAbWB04evUnvaVZZY1am98xSX0bLNPzZZYGgmZMSemaDw130 provenance
has publication info: NP55764.RAbWB04evUnvaVZZY1am98xSX0bLNPzZZYGgmZMSemaDw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55764.RAbWB04evUnvaVZZY1am98xSX0bLNPzZZYGgmZMSemaDw130 assertion
type: Assertion
description: [Our data suggest that the FAS 1377G>A and IL10 592C>A polymorphisms could modify disease-free and overall survival in women with lymph node-positive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20204402
was generated by: ECO_0000203

NP55766.RAXI8pk9mb0fij91PpaLyOmTlpHOiNUjBolOo7ToKlHds
has assertion: NP55766.RAXI8pk9mb0fij91PpaLyOmTlpHOiNUjBolOo7ToKlHds130 assertion
has provenance: NP55766.RAXI8pk9mb0fij91PpaLyOmTlpHOiNUjBolOo7ToKlHds130 provenance
has publication info: NP55766.RAXI8pk9mb0fij91PpaLyOmTlpHOiNUjBolOo7ToKlHds130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55766.RAXI8pk9mb0fij91PpaLyOmTlpHOiNUjBolOo7ToKlHds130 assertion
type: Assertion
description: [The BglII gene polymorphism of the alpha2beta1 integrin, which is a platelet collagen receptor, has been suggested as a genetic risk factor for diabetic retinopathy in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12938014
was generated by: ECO_0000203

NP55767.RAcwCRZEasZ5UY2qOd0boMmsl8qpcrGXAYI1F6kAH5kNk
has assertion: NP55767.RAcwCRZEasZ5UY2qOd0boMmsl8qpcrGXAYI1F6kAH5kNk130 assertion
has provenance: NP55767.RAcwCRZEasZ5UY2qOd0boMmsl8qpcrGXAYI1F6kAH5kNk130 provenance
has publication info: NP55767.RAcwCRZEasZ5UY2qOd0boMmsl8qpcrGXAYI1F6kAH5kNk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55767.RAcwCRZEasZ5UY2qOd0boMmsl8qpcrGXAYI1F6kAH5kNk130 assertion
type: Assertion
description: [Diabetes duration may modify the association between genetic variation in the glycoprotein Ia subunit of the platelet collagen receptor and risk of severe diabetic retinopathy: a working hypothesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12540964
was generated by: ECO_0000203

NP55773.RAUthqYW04hQZSzQ8PPEJHZw 5K4ASwWYUwmDXtZbToyw
has assertion: NP55773.RAUthqYW04hQZSzQ8PPEJHZw 5K4ASwWYUwmDXtZbToyw130 assertion
has provenance: NP55773.RAUthqYW04hQZSzQ8PPEJHZw 5K4ASwWYUwmDXtZbToyw130 provenance
has publication info: NP55773.RAUthqYW04hQZSzQ8PPEJHZw 5K4ASwWYUwmDXtZbToyw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55773.RAUthqYW04hQZSzQ8PPEJHZw 5K4ASwWYUwmDXtZbToyw130 assertion
type: Assertion
description: [ These data suggest that Pl(A2) carriers, especially those who are ACE DD, are statistically less prevalent among older healthy blood donors compared with their younger counterparts. These observations suggest an important, deleterious, time-dependent impact of the Pl(A2) allele, as well as the ACE DD/Pl(A2) allelic combination, on overall health and longevity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11568114
was generated by: ECO_0000203

NP55774.RATFbLZ0l8QSBvAP7oLxPi bJYF667ZE5Io7gJaF6q2ug
has assertion: NP55774.RATFbLZ0l8QSBvAP7oLxPi bJYF667ZE5Io7gJaF6q2ug130 assertion
has provenance: NP55774.RATFbLZ0l8QSBvAP7oLxPi bJYF667ZE5Io7gJaF6q2ug130 provenance
has publication info: NP55774.RATFbLZ0l8QSBvAP7oLxPi bJYF667ZE5Io7gJaF6q2ug130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55774.RATFbLZ0l8QSBvAP7oLxPi bJYF667ZE5Io7gJaF6q2ug130 assertion
type: Assertion
description: [Our data indicate hat patients with BD are affected by the glycoprotein Ia gene 807TT genotypes and carrying 807T allele. The risk of thrombosis is significantly higher in patients who have 807TT and 807CT genotypes than in patients who have 807CC genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12412731
was generated by: ECO_0000203

NP55776.RARWvBRo2FnOrYmODXZzNUVsZzgqDBLOftl1ANJgEtWQE
has assertion: NP55776.RARWvBRo2FnOrYmODXZzNUVsZzgqDBLOftl1ANJgEtWQE130 assertion
has provenance: NP55776.RARWvBRo2FnOrYmODXZzNUVsZzgqDBLOftl1ANJgEtWQE130 provenance
has publication info: NP55776.RARWvBRo2FnOrYmODXZzNUVsZzgqDBLOftl1ANJgEtWQE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55776.RARWvBRo2FnOrYmODXZzNUVsZzgqDBLOftl1ANJgEtWQE130 assertion
type: Assertion
description: [The aim of our study was to investigate whether common polymorphisms in the genes regulating the early insulin signalling pathway (insulin; A-23T, insulin-like growth factor 1 receptor IGF-1R; GAG1013GAA, plasma cell membrane glycoprotein 1 PC-1; K121Q, insulin receptor substrate IRS-1; G972R, insulin receptor substrate 2 IRS-2; G1057D and phosphatidylinositol 3-kinase p85 alpha PI3K; M326I) affect the weight change and development of Type 2 diabetes in the Finnish Diabetes Prevention Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15127203
was generated by: ECO_0000203

NP55777.RAQCSfUgjjw4j6nUdP716yaq0R3dtJqzoAPM7A UwlQKQ
has assertion: NP55777.RAQCSfUgjjw4j6nUdP716yaq0R3dtJqzoAPM7A UwlQKQ130 assertion
has provenance: NP55777.RAQCSfUgjjw4j6nUdP716yaq0R3dtJqzoAPM7A UwlQKQ130 provenance
has publication info: NP55777.RAQCSfUgjjw4j6nUdP716yaq0R3dtJqzoAPM7A UwlQKQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55777.RAQCSfUgjjw4j6nUdP716yaq0R3dtJqzoAPM7A UwlQKQ130 assertion
type: Assertion
description: [These data provide evidence for a strong association between type 2 diabetes and the G1057D common genetic variant of IRS-2, which appears to be protective against type 2 diabetes in a codominant fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11030756
was generated by: ECO_0000203

NP55779.RAZ77kjLvD-67Y3DUyrJuZPPGDjid2zW5tl8V4hL-CLHg
has assertion: NP55779.RAZ77kjLvD-67Y3DUyrJuZPPGDjid2zW5tl8V4hL-CLHg130 assertion
has provenance: NP55779.RAZ77kjLvD-67Y3DUyrJuZPPGDjid2zW5tl8V4hL-CLHg130 provenance
has publication info: NP55779.RAZ77kjLvD-67Y3DUyrJuZPPGDjid2zW5tl8V4hL-CLHg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55779.RAZ77kjLvD-67Y3DUyrJuZPPGDjid2zW5tl8V4hL-CLHg130 assertion
type: Assertion
description: [New amino acid substitutions in the IRS-2 gene in Finnish and Chinese subjects with late-onset type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11473060
was generated by: ECO_0000203

NP55780.RAWeUEPglWZVcci Xb9Srt2qJPLvJF QHIbpO2euWKcb0
has assertion: NP55780.RAWeUEPglWZVcci Xb9Srt2qJPLvJF QHIbpO2euWKcb0130 assertion
has provenance: NP55780.RAWeUEPglWZVcci Xb9Srt2qJPLvJF QHIbpO2euWKcb0130 provenance
has publication info: NP55780.RAWeUEPglWZVcci Xb9Srt2qJPLvJF QHIbpO2euWKcb0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55780.RAWeUEPglWZVcci Xb9Srt2qJPLvJF QHIbpO2euWKcb0130 assertion
type: Assertion
description: [The aim of this study was to investigate the association of Gly1057Asp polymorphism in insulin receptor substrate-2 (IRS-2) gene among patients with type 2 diabetes in well defined ethnic groups from Djerba Island in Southeastern Tunisia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19332049
was generated by: ECO_0000203

NP55783.RAcDbqAkQmjEtTEsNxJSxTyCXQ9XOV1F8i cB3VhiEx-w
has assertion: NP55783.RAcDbqAkQmjEtTEsNxJSxTyCXQ9XOV1F8i cB3VhiEx-w130 assertion
has provenance: NP55783.RAcDbqAkQmjEtTEsNxJSxTyCXQ9XOV1F8i cB3VhiEx-w130 provenance
has publication info: NP55783.RAcDbqAkQmjEtTEsNxJSxTyCXQ9XOV1F8i cB3VhiEx-w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55783.RAcDbqAkQmjEtTEsNxJSxTyCXQ9XOV1F8i cB3VhiEx-w130 assertion
type: Assertion
description: [we found limited evidence for a role of gene variants of the insulin signaling pathway and prevalence of advanced colorectal adenoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17416760
was generated by: ECO_0000203

NP55792.RAcMdmczp94xaq8r1I7W5oJWpBYbTUBf7-kAGVDAIdmpE
has assertion: NP55792.RAcMdmczp94xaq8r1I7W5oJWpBYbTUBf7-kAGVDAIdmpE130 assertion
has provenance: NP55792.RAcMdmczp94xaq8r1I7W5oJWpBYbTUBf7-kAGVDAIdmpE130 provenance
has publication info: NP55792.RAcMdmczp94xaq8r1I7W5oJWpBYbTUBf7-kAGVDAIdmpE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55792.RAcMdmczp94xaq8r1I7W5oJWpBYbTUBf7-kAGVDAIdmpE130 assertion
type: Assertion
description: [Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18992148
was generated by: ECO_0000203

NP55796.RAeV1ablvuDdlN33DOf1deQ3BJpF6g8D0uKpptSy0MqEk
has assertion: NP55796.RAeV1ablvuDdlN33DOf1deQ3BJpF6g8D0uKpptSy0MqEk130 assertion
has provenance: NP55796.RAeV1ablvuDdlN33DOf1deQ3BJpF6g8D0uKpptSy0MqEk130 provenance
has publication info: NP55796.RAeV1ablvuDdlN33DOf1deQ3BJpF6g8D0uKpptSy0MqEk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55796.RAeV1ablvuDdlN33DOf1deQ3BJpF6g8D0uKpptSy0MqEk130 assertion
type: Assertion
description: [A study of the single nucleotide polymorphism in seven genes (GHR, IGFBP3, IGFR1, IRS1, FMN1, ANXA2, TaGLN) in ethnic Russians and in patients with prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20540360
was generated by: ECO_0000203

NP55802.RAc5yiBjwYQ3iavGn5HABMo8GYSdzIhfUeVGIrJIk8jME
has assertion: NP55802.RAc5yiBjwYQ3iavGn5HABMo8GYSdzIhfUeVGIrJIk8jME130 assertion
has provenance: NP55802.RAc5yiBjwYQ3iavGn5HABMo8GYSdzIhfUeVGIrJIk8jME130 provenance
has publication info: NP55802.RAc5yiBjwYQ3iavGn5HABMo8GYSdzIhfUeVGIrJIk8jME130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55802.RAc5yiBjwYQ3iavGn5HABMo8GYSdzIhfUeVGIrJIk8jME130 assertion
type: Assertion
description: [The gene encoding insulin receptor substrate-1 (IRS1) represents a strong biological candidate for a contributory role in type 2 diabetes susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15561966
was generated by: ECO_0000203

NP55806.RAXr2gilML-hPzJKx4m9tRAZUC 0aWgnTDqIlXDuaV7Us
has assertion: NP55806.RAXr2gilML-hPzJKx4m9tRAZUC 0aWgnTDqIlXDuaV7Us130 assertion
has provenance: NP55806.RAXr2gilML-hPzJKx4m9tRAZUC 0aWgnTDqIlXDuaV7Us130 provenance
has publication info: NP55806.RAXr2gilML-hPzJKx4m9tRAZUC 0aWgnTDqIlXDuaV7Us130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55806.RAXr2gilML-hPzJKx4m9tRAZUC 0aWgnTDqIlXDuaV7Us130 assertion
type: Assertion
description: [Considering their key role in both insulin action and insulin secretion, IRS-1 and IRS-2 molecules have been considered plausible candidate genes involved in the pathogenesis of Type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11256583
was generated by: ECO_0000203

NP55808.RAT-ybHOIqaaJkE-1oL9gnM4UfwBeSzgLRoGF8GrUcmCY
has assertion: NP55808.RAT-ybHOIqaaJkE-1oL9gnM4UfwBeSzgLRoGF8GrUcmCY130 assertion
has provenance: NP55808.RAT-ybHOIqaaJkE-1oL9gnM4UfwBeSzgLRoGF8GrUcmCY130 provenance
has publication info: NP55808.RAT-ybHOIqaaJkE-1oL9gnM4UfwBeSzgLRoGF8GrUcmCY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55808.RAT-ybHOIqaaJkE-1oL9gnM4UfwBeSzgLRoGF8GrUcmCY130 assertion
type: Assertion
description: [These results suggest that the Arg(972) IRS-1 variant could contribute to the risk for atherosclerotic cardiovascular diseases associated with type 2 diabetes by producing a cluster of insulin resistance-related metabolic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12843189
was generated by: ECO_0000203

NP55811.RAe1qOrAzSfNGCD07mPME-d4PwAUO-ie40chIFU1sJMtA
has assertion: NP55811.RAe1qOrAzSfNGCD07mPME-d4PwAUO-ie40chIFU1sJMtA130 assertion
has provenance: NP55811.RAe1qOrAzSfNGCD07mPME-d4PwAUO-ie40chIFU1sJMtA130 provenance
has publication info: NP55811.RAe1qOrAzSfNGCD07mPME-d4PwAUO-ie40chIFU1sJMtA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55811.RAe1qOrAzSfNGCD07mPME-d4PwAUO-ie40chIFU1sJMtA130 assertion
type: Assertion
description: [In order to investigate whether the variances in the candidate genes (Insulin receptor substrate IRS-1, beta3-adrenergic receptor ADRB3, 3 beta-hydro-xysteroid dehydrogenase HSD3B2, glucocorticoid receptor GRL and 21-hydroxylase CYP21) which affect the metabolism of adrenal steroids hormone and body composition, are associated with precocious puberty in Chinese girls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16648810
was generated by: ECO_0000203

NP55818.RAddPQe-7ed-3pr4NFJSQPF5EnzMWTkiUaeKSMiZTnNnU
has assertion: NP55818.RAddPQe-7ed-3pr4NFJSQPF5EnzMWTkiUaeKSMiZTnNnU130 assertion
has provenance: NP55818.RAddPQe-7ed-3pr4NFJSQPF5EnzMWTkiUaeKSMiZTnNnU130 provenance
has publication info: NP55818.RAddPQe-7ed-3pr4NFJSQPF5EnzMWTkiUaeKSMiZTnNnU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55818.RAddPQe-7ed-3pr4NFJSQPF5EnzMWTkiUaeKSMiZTnNnU130 assertion
type: Assertion
description: [Lack of association of the Gly972Arg mutation of the insulin receptor substrate-1 gene with coronary artery disease in the Austrian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14687252
was generated by: ECO_0000203

NP55825.RAd3fud67z1gopYuk2lwglx DdpMUzCDqtrV9bLway3lc
has assertion: NP55825.RAd3fud67z1gopYuk2lwglx DdpMUzCDqtrV9bLway3lc130 assertion
has provenance: NP55825.RAd3fud67z1gopYuk2lwglx DdpMUzCDqtrV9bLway3lc130 provenance
has publication info: NP55825.RAd3fud67z1gopYuk2lwglx DdpMUzCDqtrV9bLway3lc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55825.RAd3fud67z1gopYuk2lwglx DdpMUzCDqtrV9bLway3lc130 assertion
type: Assertion
description: [our results help to understand the role of the IRF5 locus in SLE susceptibility by clearly separating protection from susceptibility as caused by independent polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17568788
was generated by: ECO_0000203

NP55826.RASILmHuN77QkHS 6BbA9tIJNNN74CMf40-7qHm4xA8Ag
has assertion: NP55826.RASILmHuN77QkHS 6BbA9tIJNNN74CMf40-7qHm4xA8Ag130 assertion
has provenance: NP55826.RASILmHuN77QkHS 6BbA9tIJNNN74CMf40-7qHm4xA8Ag130 provenance
has publication info: NP55826.RASILmHuN77QkHS 6BbA9tIJNNN74CMf40-7qHm4xA8Ag130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55826.RASILmHuN77QkHS 6BbA9tIJNNN74CMf40-7qHm4xA8Ag130 assertion
type: Assertion
description: [Genetic association of IRF5 with SLE in Mexicans: higher frequency of the risk haplotype and its homozygozity than Europeans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17476532
was generated by: ECO_0000203

NP55827.RAer f4Fdf3E3ni0aOaJ3SiysBguHBNweJT6XUDI0asG8
has assertion: NP55827.RAer f4Fdf3E3ni0aOaJ3SiysBguHBNweJT6XUDI0asG8130 assertion
has provenance: NP55827.RAer f4Fdf3E3ni0aOaJ3SiysBguHBNweJT6XUDI0asG8130 provenance
has publication info: NP55827.RAer f4Fdf3E3ni0aOaJ3SiysBguHBNweJT6XUDI0asG8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55827.RAer f4Fdf3E3ni0aOaJ3SiysBguHBNweJT6XUDI0asG8130 assertion
type: Assertion
description: [An association between JIA and a previously unreported 3'UTR polymorphism of IRF-1 was observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11315919
was generated by: ECO_0000203

NP55833.RAWs iOZEORVNU2hXNGatfbf1BOABCLjr4KyimU1OMMBo
has assertion: NP55833.RAWs iOZEORVNU2hXNGatfbf1BOABCLjr4KyimU1OMMBo130 assertion
has provenance: NP55833.RAWs iOZEORVNU2hXNGatfbf1BOABCLjr4KyimU1OMMBo130 provenance
has publication info: NP55833.RAWs iOZEORVNU2hXNGatfbf1BOABCLjr4KyimU1OMMBo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55833.RAWs iOZEORVNU2hXNGatfbf1BOABCLjr4KyimU1OMMBo130 assertion
type: Assertion
description: [Genetic epidemiology of juvenile idiopathic arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12195624
was generated by: ECO_0000203

NP55834.RAWGjbj6d8xc6Aow79rJbJOSvOJzp7BZu20uo-tZ6Oruw
has assertion: NP55834.RAWGjbj6d8xc6Aow79rJbJOSvOJzp7BZu20uo-tZ6Oruw130 assertion
has provenance: NP55834.RAWGjbj6d8xc6Aow79rJbJOSvOJzp7BZu20uo-tZ6Oruw130 provenance
has publication info: NP55834.RAWGjbj6d8xc6Aow79rJbJOSvOJzp7BZu20uo-tZ6Oruw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55834.RAWGjbj6d8xc6Aow79rJbJOSvOJzp7BZu20uo-tZ6Oruw130 assertion
type: Assertion
description: [DNA from 765 patients with JIA and 508 unaffected control subjects was genotyped for 4 single-nucleotide polymorphisms in the IRF-1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17328074
was generated by: ECO_0000203

NP55835.RAfCR-DeC9mIj8edh33I-7cIwCFEeHsv16hzRnkFX2Dh8
has assertion: NP55835.RAfCR-DeC9mIj8edh33I-7cIwCFEeHsv16hzRnkFX2Dh8130 assertion
has provenance: NP55835.RAfCR-DeC9mIj8edh33I-7cIwCFEeHsv16hzRnkFX2Dh8130 provenance
has publication info: NP55835.RAfCR-DeC9mIj8edh33I-7cIwCFEeHsv16hzRnkFX2Dh8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55835.RAfCR-DeC9mIj8edh33I-7cIwCFEeHsv16hzRnkFX2Dh8130 assertion
type: Assertion
description: [Genetic epidemiology of juvenile idiopathic arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12195624
was generated by: ECO_0000203

NP55838.RAVYRGBpK4V-UhTvRBoWgEnvR8wZIqii4hneGcpm6f3oY
has assertion: NP55838.RAVYRGBpK4V-UhTvRBoWgEnvR8wZIqii4hneGcpm6f3oY130 assertion
has provenance: NP55838.RAVYRGBpK4V-UhTvRBoWgEnvR8wZIqii4hneGcpm6f3oY130 provenance
has publication info: NP55838.RAVYRGBpK4V-UhTvRBoWgEnvR8wZIqii4hneGcpm6f3oY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55838.RAVYRGBpK4V-UhTvRBoWgEnvR8wZIqii4hneGcpm6f3oY130 assertion
type: Assertion
description: [Association study between the IL4, IL13, IRF1 and UGRP1 genes in chromosomal 5q31 region and Chinese Graves' disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16195814
was generated by: ECO_0000203

NP55849.RAQTZAJNqrZbHhqjQEEDNtizkZF30xluJuu50dwfLrWHY
has assertion: NP55849.RAQTZAJNqrZbHhqjQEEDNtizkZF30xluJuu50dwfLrWHY130 assertion
has provenance: NP55849.RAQTZAJNqrZbHhqjQEEDNtizkZF30xluJuu50dwfLrWHY130 provenance
has publication info: NP55849.RAQTZAJNqrZbHhqjQEEDNtizkZF30xluJuu50dwfLrWHY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55849.RAQTZAJNqrZbHhqjQEEDNtizkZF30xluJuu50dwfLrWHY130 assertion
type: Assertion
description: [Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16873704
was generated by: ECO_0000203

NP55859.RAXv7DVGWdbabhhhpboiAENRwdL3wLgzfMBK 8Fq-DTjE
has assertion: NP55859.RAXv7DVGWdbabhhhpboiAENRwdL3wLgzfMBK 8Fq-DTjE130 assertion
has provenance: NP55859.RAXv7DVGWdbabhhhpboiAENRwdL3wLgzfMBK 8Fq-DTjE130 provenance
has publication info: NP55859.RAXv7DVGWdbabhhhpboiAENRwdL3wLgzfMBK 8Fq-DTjE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55859.RAXv7DVGWdbabhhhpboiAENRwdL3wLgzfMBK 8Fq-DTjE130 assertion
type: Assertion
description: [DNA polymorphisms of the insulin receptor gene and non-insulin-dependent diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/2894731
was generated by: ECO_0000203

NP55861.RAV IIBvsv1DTQXf-9DyM6HxNib9 YPVEv1g3zfPjfjmg
has assertion: NP55861.RAV IIBvsv1DTQXf-9DyM6HxNib9 YPVEv1g3zfPjfjmg130 assertion
has provenance: NP55861.RAV IIBvsv1DTQXf-9DyM6HxNib9 YPVEv1g3zfPjfjmg130 provenance
has publication info: NP55861.RAV IIBvsv1DTQXf-9DyM6HxNib9 YPVEv1g3zfPjfjmg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55861.RAV IIBvsv1DTQXf-9DyM6HxNib9 YPVEv1g3zfPjfjmg130 assertion
type: Assertion
description: [Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: linkage of candidate genes using two sib-pair based variance components analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18828733
was generated by: ECO_0000203

NP55863.RAdXX lDQN OU3gyC3OCQz8uVa-JWatN cbJtTXcGYAn4
has assertion: NP55863.RAdXX lDQN OU3gyC3OCQz8uVa-JWatN cbJtTXcGYAn4130 assertion
has provenance: NP55863.RAdXX lDQN OU3gyC3OCQz8uVa-JWatN cbJtTXcGYAn4130 provenance
has publication info: NP55863.RAdXX lDQN OU3gyC3OCQz8uVa-JWatN cbJtTXcGYAn4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55863.RAdXX lDQN OU3gyC3OCQz8uVa-JWatN cbJtTXcGYAn4130 assertion
type: Assertion
description: [In conclusion, our results suggested that a susceptibility gene for PCOS was located on chromosome 19p13.3 in the insulin receptor gene region. It remains to be determined if this susceptibility gene is the insulin receptor gene itself or a closely located gene. Since insulin stimulates androgen secretion by the ovarian stroma it is likely that INSR function in the ovary is involved in the genetic susceptibility ot PCOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11232039
was generated by: ECO_0000203

NP55867.RAVmP2nDn2zGK708 5cN8cGr-seypQhMx6UGlHJPwJZF4
has assertion: NP55867.RAVmP2nDn2zGK708 5cN8cGr-seypQhMx6UGlHJPwJZF4130 assertion
has provenance: NP55867.RAVmP2nDn2zGK708 5cN8cGr-seypQhMx6UGlHJPwJZF4130 provenance
has publication info: NP55867.RAVmP2nDn2zGK708 5cN8cGr-seypQhMx6UGlHJPwJZF4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55867.RAVmP2nDn2zGK708 5cN8cGr-seypQhMx6UGlHJPwJZF4130 assertion
type: Assertion
description: [DNA samples from forty-four adolescent girls with PCOS and 50 healthy controls were analyzed by PCR-RFLP and direct DNA sequencing to determine the genotypic frequency of 17 different polymorphic loci on the FSHR (A307T, N680S), CYP17 (-34 T/C), CYP1A1 (T6235C), CAPN10 (44, 43, 19, 63), INSR (exon 17 C/T), SERPINE1 (4G/5G) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19387820
was generated by: ECO_0000203

NP55873.RAejYR27nNZxRjO0C3vwEBXTJPIKw4SJS6xpu2SJUjHRU
has assertion: NP55873.RAejYR27nNZxRjO0C3vwEBXTJPIKw4SJS6xpu2SJUjHRU130 assertion
has provenance: NP55873.RAejYR27nNZxRjO0C3vwEBXTJPIKw4SJS6xpu2SJUjHRU130 provenance
has publication info: NP55873.RAejYR27nNZxRjO0C3vwEBXTJPIKw4SJS6xpu2SJUjHRU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55873.RAejYR27nNZxRjO0C3vwEBXTJPIKw4SJS6xpu2SJUjHRU130 assertion
type: Assertion
description: [Insulin receptor gene polymorphism in myocardial infarction patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12420346
was generated by: ECO_0000203

NP55875.RAdPOUXf2k82b-ZbbTlySGvKnnGNrM303b4DbmUrrFklw
has assertion: NP55875.RAdPOUXf2k82b-ZbbTlySGvKnnGNrM303b4DbmUrrFklw130 assertion
has provenance: NP55875.RAdPOUXf2k82b-ZbbTlySGvKnnGNrM303b4DbmUrrFklw130 provenance
has publication info: NP55875.RAdPOUXf2k82b-ZbbTlySGvKnnGNrM303b4DbmUrrFklw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55875.RAdPOUXf2k82b-ZbbTlySGvKnnGNrM303b4DbmUrrFklw130 assertion
type: Assertion
description: [The present study thus suggests that there could be a relationship of plasma angiotensinogen with INSR genotype, and of each with hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/8740916
was generated by: ECO_0000203

NP55876.RAeIDUbOY1rbyLnb f 5wp5jwn02SabEjkj4ydWenaqKA
has assertion: NP55876.RAeIDUbOY1rbyLnb f 5wp5jwn02SabEjkj4ydWenaqKA130 assertion
has provenance: NP55876.RAeIDUbOY1rbyLnb f 5wp5jwn02SabEjkj4ydWenaqKA130 provenance
has publication info: NP55876.RAeIDUbOY1rbyLnb f 5wp5jwn02SabEjkj4ydWenaqKA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55876.RAeIDUbOY1rbyLnb f 5wp5jwn02SabEjkj4ydWenaqKA130 assertion
type: Assertion
description: [Association of a RFLP for the insulin receptor gene, but not insulin, with essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/1683535
was generated by: ECO_0000203

NP55878.RARUTSLiDKQ JwRq1JshZNPj Sg-RTDEF2nkX2uylE064
has assertion: NP55878.RARUTSLiDKQ JwRq1JshZNPj Sg-RTDEF2nkX2uylE064130 assertion
has provenance: NP55878.RARUTSLiDKQ JwRq1JshZNPj Sg-RTDEF2nkX2uylE064130 provenance
has publication info: NP55878.RARUTSLiDKQ JwRq1JshZNPj Sg-RTDEF2nkX2uylE064130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55878.RARUTSLiDKQ JwRq1JshZNPj Sg-RTDEF2nkX2uylE064130 assertion
type: Assertion
description: [An in-frame insertion in exon 3 and a nonsense mutation in exon 2 of the insulin receptor gene associated with severe insulin resistance in a patient with Rabson-Mendenhall syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/8270132
was generated by: ECO_0000203

NP55895.RAem wTBCznjbGyjY6 kSnAE1kE2VEg6t lJcCqiQ0qLk
has assertion: NP55895.RAem wTBCznjbGyjY6 kSnAE1kE2VEg6t lJcCqiQ0qLk130 assertion
has provenance: NP55895.RAem wTBCznjbGyjY6 kSnAE1kE2VEg6t lJcCqiQ0qLk130 provenance
has publication info: NP55895.RAem wTBCznjbGyjY6 kSnAE1kE2VEg6t lJcCqiQ0qLk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55895.RAem wTBCznjbGyjY6 kSnAE1kE2VEg6t lJcCqiQ0qLk130 assertion
type: Assertion
description: [Candidate gene association study in type 2 diabetes indicates a role for genes involved in beta-cell function as well as insulin action.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14551916
was generated by: ECO_0000203

NP55897.RAU5gX9To0ghuIRKlp47DdRNgVmuxu19UF mYkE72RDgU
has assertion: NP55897.RAU5gX9To0ghuIRKlp47DdRNgVmuxu19UF mYkE72RDgU130 assertion
has provenance: NP55897.RAU5gX9To0ghuIRKlp47DdRNgVmuxu19UF mYkE72RDgU130 provenance
has publication info: NP55897.RAU5gX9To0ghuIRKlp47DdRNgVmuxu19UF mYkE72RDgU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55897.RAU5gX9To0ghuIRKlp47DdRNgVmuxu19UF mYkE72RDgU130 assertion
type: Assertion
description: [We investigated the contribution of Type 1 diabetes susceptibility genes to the progression of the insulin-deficient state and mode of onset of Type 2 diabetes in GAD Ab-positive (GAD-Ab+) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11606170
was generated by: ECO_0000203

NP55901.RAY1howQTFnUiIy6mnZ1ghtkoCZTEq31u72ef TqnI0Xs
has assertion: NP55901.RAY1howQTFnUiIy6mnZ1ghtkoCZTEq31u72ef TqnI0Xs130 assertion
has provenance: NP55901.RAY1howQTFnUiIy6mnZ1ghtkoCZTEq31u72ef TqnI0Xs130 provenance
has publication info: NP55901.RAY1howQTFnUiIy6mnZ1ghtkoCZTEq31u72ef TqnI0Xs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55901.RAY1howQTFnUiIy6mnZ1ghtkoCZTEq31u72ef TqnI0Xs130 assertion
type: Assertion
description: [Possible correlation between non-insulin dependent diabetes mellitus (NIDDM) and restriction fragment length polymorphism (RFLP) of the 5'-flanking region of insulin gene in Korean diabetic population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/2908729
was generated by: ECO_0000203

NP55903.RAZ5vp3B-pkT8QC1ggyjWbvpoJo4RBr8JExxX wxyaToQ
has assertion: NP55903.RAZ5vp3B-pkT8QC1ggyjWbvpoJo4RBr8JExxX wxyaToQ130 assertion
has provenance: NP55903.RAZ5vp3B-pkT8QC1ggyjWbvpoJo4RBr8JExxX wxyaToQ130 provenance
has publication info: NP55903.RAZ5vp3B-pkT8QC1ggyjWbvpoJo4RBr8JExxX wxyaToQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55903.RAZ5vp3B-pkT8QC1ggyjWbvpoJo4RBr8JExxX wxyaToQ130 assertion
type: Assertion
description: [In the Sikhs no association with non-insulin-dependent diabetes mellitus was seen with the hypervariable region of the insulin gene or with HLA-DR/DQ/DX alpha chain restriction fragment length polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/2892607
was generated by: ECO_0000203

NP55926.RAUtwPoCiKy7VIP2uXvZFrwFMAEi5Gw5 3mHeEw zoNw4
has assertion: NP55926.RAUtwPoCiKy7VIP2uXvZFrwFMAEi5Gw5 3mHeEw zoNw4130 assertion
has provenance: NP55926.RAUtwPoCiKy7VIP2uXvZFrwFMAEi5Gw5 3mHeEw zoNw4130 provenance
has publication info: NP55926.RAUtwPoCiKy7VIP2uXvZFrwFMAEi5Gw5 3mHeEw zoNw4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55926.RAUtwPoCiKy7VIP2uXvZFrwFMAEi5Gw5 3mHeEw zoNw4130 assertion
type: Assertion
description: [The use of DNA analysis for diagnostics of hereditary premature ovarian failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16161415
was generated by: ECO_0000203

NP55927.RAfaY7sjBxfsueHQ0splxHIGol4rifPt9U8S0atnlhT2w
has assertion: NP55927.RAfaY7sjBxfsueHQ0splxHIGol4rifPt9U8S0atnlhT2w130 assertion
has provenance: NP55927.RAfaY7sjBxfsueHQ0splxHIGol4rifPt9U8S0atnlhT2w130 provenance
has publication info: NP55927.RAfaY7sjBxfsueHQ0splxHIGol4rifPt9U8S0atnlhT2w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55927.RAfaY7sjBxfsueHQ0splxHIGol4rifPt9U8S0atnlhT2w130 assertion
type: Assertion
description: [ These data strengthen the concept of the INHalpha gene as a candidate for ovarian failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12093833
was generated by: ECO_0000203

NP55934.RAVPE-o iTuxFEcrVxk4tFVWMl4a09ZVY0NREXr 4I5bw
has assertion: NP55934.RAVPE-o iTuxFEcrVxk4tFVWMl4a09ZVY0NREXr 4I5bw130 assertion
has provenance: NP55934.RAVPE-o iTuxFEcrVxk4tFVWMl4a09ZVY0NREXr 4I5bw130 provenance
has publication info: NP55934.RAVPE-o iTuxFEcrVxk4tFVWMl4a09ZVY0NREXr 4I5bw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55934.RAVPE-o iTuxFEcrVxk4tFVWMl4a09ZVY0NREXr 4I5bw130 assertion
type: Assertion
description: [ Variants in the inhibin alpha gene are strongly associated with premature ovarian failure in Indian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19324345
was generated by: ECO_0000203

NP55936.RAQVJaDdo82eMJms8dlZTR9sKGpqqKwi-H1emlKgnrjxU
has assertion: NP55936.RAQVJaDdo82eMJms8dlZTR9sKGpqqKwi-H1emlKgnrjxU130 assertion
has provenance: NP55936.RAQVJaDdo82eMJms8dlZTR9sKGpqqKwi-H1emlKgnrjxU130 provenance
has publication info: NP55936.RAQVJaDdo82eMJms8dlZTR9sKGpqqKwi-H1emlKgnrjxU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55936.RAQVJaDdo82eMJms8dlZTR9sKGpqqKwi-H1emlKgnrjxU130 assertion
type: Assertion
description: [ The prevalence of INHalpha gene variants is not increased in PE. Due to its frequency, the 769G-->A transition may be considered a polymorphism present in the general Italian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15816368
was generated by: ECO_0000203

NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE
has assertion: NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130 assertion
has provenance: NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130 provenance
has publication info: NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130 assertion
type: Assertion
description: [There were no statistically significant allele or haplotype frequency differences between cases and controls. Therefore, these results provide no evidence that these loci are associated with CD in this sample population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15713213
was generated by: ECO_0000203

NP55945.RARw41MNO-xDD U83FBIRmPpHiv1AxQCpd1fuldvJx-jQ
has assertion: NP55945.RARw41MNO-xDD U83FBIRmPpHiv1AxQCpd1fuldvJx-jQ130 assertion
has provenance: NP55945.RARw41MNO-xDD U83FBIRmPpHiv1AxQCpd1fuldvJx-jQ130 provenance
has publication info: NP55945.RARw41MNO-xDD U83FBIRmPpHiv1AxQCpd1fuldvJx-jQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55945.RARw41MNO-xDD U83FBIRmPpHiv1AxQCpd1fuldvJx-jQ130 assertion
type: Assertion
description: [Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19845895
was generated by: ECO_0000203

NP55947.RAV5wxK1gv4keOL0425tV3pi5XPW5GwupFRvkZrDeYaI4
has assertion: NP55947.RAV5wxK1gv4keOL0425tV3pi5XPW5GwupFRvkZrDeYaI4130 assertion
has provenance: NP55947.RAV5wxK1gv4keOL0425tV3pi5XPW5GwupFRvkZrDeYaI4130 provenance
has publication info: NP55947.RAV5wxK1gv4keOL0425tV3pi5XPW5GwupFRvkZrDeYaI4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55947.RAV5wxK1gv4keOL0425tV3pi5XPW5GwupFRvkZrDeYaI4130 assertion
type: Assertion
description: [Promoter polymorphism in the candidate genes, IL-4, IL-9, TGF-beta1, for atopy and asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10224407
was generated by: ECO_0000203

NP55952.RAQBkO0jh82Q9IQCHZjVVceTlK 4HxcNm7TtGUDqJf7JM
has assertion: NP55952.RAQBkO0jh82Q9IQCHZjVVceTlK 4HxcNm7TtGUDqJf7JM130 assertion
has provenance: NP55952.RAQBkO0jh82Q9IQCHZjVVceTlK 4HxcNm7TtGUDqJf7JM130 provenance
has publication info: NP55952.RAQBkO0jh82Q9IQCHZjVVceTlK 4HxcNm7TtGUDqJf7JM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55952.RAQBkO0jh82Q9IQCHZjVVceTlK 4HxcNm7TtGUDqJf7JM130 assertion
type: Assertion
description: [ Due to its rapid and relatively inexpensive performance and accuracy, the presented allelic discrimination assay for CXCR2 polymorphisms has wide applicability, especially for high-throughput sample analysis in large population genotyping studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14967163
was generated by: ECO_0000203

NP55956.RAbg7FP4wuLSMveU-LXLBIqnUIZ w-QrIvL9cXgqeDdOs
has assertion: NP55956.RAbg7FP4wuLSMveU-LXLBIqnUIZ w-QrIvL9cXgqeDdOs130 assertion
has provenance: NP55956.RAbg7FP4wuLSMveU-LXLBIqnUIZ w-QrIvL9cXgqeDdOs130 provenance
has publication info: NP55956.RAbg7FP4wuLSMveU-LXLBIqnUIZ w-QrIvL9cXgqeDdOs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55956.RAbg7FP4wuLSMveU-LXLBIqnUIZ w-QrIvL9cXgqeDdOs130 assertion
type: Assertion
description: [Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19141999
was generated by: ECO_0000203

NP55958.RAc5su3ZSe67gzPCoxPOGWRGtQHMCr0YMFvM4mkpBwf3M
has assertion: NP55958.RAc5su3ZSe67gzPCoxPOGWRGtQHMCr0YMFvM4mkpBwf3M130 assertion
has provenance: NP55958.RAc5su3ZSe67gzPCoxPOGWRGtQHMCr0YMFvM4mkpBwf3M130 provenance
has publication info: NP55958.RAc5su3ZSe67gzPCoxPOGWRGtQHMCr0YMFvM4mkpBwf3M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55958.RAc5su3ZSe67gzPCoxPOGWRGtQHMCr0YMFvM4mkpBwf3M130 assertion
type: Assertion
description: [These findings suggest that - with the possible exception of IL-1beta- genetic variation associated with differential expression of the selected pro- and anti-inflammatory cytokines is unlikely to play a major role in susceptibility to and prognosis in CMM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14675394
was generated by: ECO_0000203

NP55973.RAXl 3Qp113CBeI6UI2EH3pgkDw8gfCA4seQZkQkC1OIA
has assertion: NP55973.RAXl 3Qp113CBeI6UI2EH3pgkDw8gfCA4seQZkQkC1OIA130 assertion
has provenance: NP55973.RAXl 3Qp113CBeI6UI2EH3pgkDw8gfCA4seQZkQkC1OIA130 provenance
has publication info: NP55973.RAXl 3Qp113CBeI6UI2EH3pgkDw8gfCA4seQZkQkC1OIA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55973.RAXl 3Qp113CBeI6UI2EH3pgkDw8gfCA4seQZkQkC1OIA130 assertion
type: Assertion
description: [Polymorphisms in inflammation-related genes and risk of gastric cancer (Finland).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16411061
was generated by: ECO_0000203

NP55976.RAWhdy-h7bptkv6tLqZHo Gf48iJ5YXFaJnkTdy8y1FwU
has assertion: NP55976.RAWhdy-h7bptkv6tLqZHo Gf48iJ5YXFaJnkTdy8y1FwU130 assertion
has provenance: NP55976.RAWhdy-h7bptkv6tLqZHo Gf48iJ5YXFaJnkTdy8y1FwU130 provenance
has publication info: NP55976.RAWhdy-h7bptkv6tLqZHo Gf48iJ5YXFaJnkTdy8y1FwU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55976.RAWhdy-h7bptkv6tLqZHo Gf48iJ5YXFaJnkTdy8y1FwU130 assertion
type: Assertion
description: [This study showed that the IL8-251*A allele could be related to the development of distal gastric cancer in this Mexican population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17462092
was generated by: ECO_0000203

NP55977.RAZt-AC2h2WZoBc-13NLMS l yQQ302O8ygPkolYHBOGk
has assertion: NP55977.RAZt-AC2h2WZoBc-13NLMS l yQQ302O8ygPkolYHBOGk130 assertion
has provenance: NP55977.RAZt-AC2h2WZoBc-13NLMS l yQQ302O8ygPkolYHBOGk130 provenance
has publication info: NP55977.RAZt-AC2h2WZoBc-13NLMS l yQQ302O8ygPkolYHBOGk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55977.RAZt-AC2h2WZoBc-13NLMS l yQQ302O8ygPkolYHBOGk130 assertion
type: Assertion
description: [A systematic review of meta-analyses on gene polymorphisms and gastric cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19506726
was generated by: ECO_0000203

NP55983.RAfPZQkA- NQer4Q0ecnvr1BDulfgDSkvWXfuGSGbRomY
has assertion: NP55983.RAfPZQkA- NQer4Q0ecnvr1BDulfgDSkvWXfuGSGbRomY130 assertion
has provenance: NP55983.RAfPZQkA- NQer4Q0ecnvr1BDulfgDSkvWXfuGSGbRomY130 provenance
has publication info: NP55983.RAfPZQkA- NQer4Q0ecnvr1BDulfgDSkvWXfuGSGbRomY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55983.RAfPZQkA- NQer4Q0ecnvr1BDulfgDSkvWXfuGSGbRomY130 assertion
type: Assertion
description: [Our prospective study suggests that genetic variation in IL10 and possibly TLR4 is associated with prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19267370
was generated by: ECO_0000203

NP55990.RAVSGIkT1FIRlhtzOQpPKJ1Qbrz2Rhbuv8YhAHPyRlnqs
has assertion: NP55990.RAVSGIkT1FIRlhtzOQpPKJ1Qbrz2Rhbuv8YhAHPyRlnqs130 assertion
has provenance: NP55990.RAVSGIkT1FIRlhtzOQpPKJ1Qbrz2Rhbuv8YhAHPyRlnqs130 provenance
has publication info: NP55990.RAVSGIkT1FIRlhtzOQpPKJ1Qbrz2Rhbuv8YhAHPyRlnqs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55990.RAVSGIkT1FIRlhtzOQpPKJ1Qbrz2Rhbuv8YhAHPyRlnqs130 assertion
type: Assertion
description: [Role of inflammation gene polymorphisms on pain severity in lung cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19773451
was generated by: ECO_0000203

NP55998.RAS57evhd7XKASoDC6JK-cnSxWCHB0GsgJYvI44VgVjTs
has assertion: NP55998.RAS57evhd7XKASoDC6JK-cnSxWCHB0GsgJYvI44VgVjTs130 assertion
has provenance: NP55998.RAS57evhd7XKASoDC6JK-cnSxWCHB0GsgJYvI44VgVjTs130 provenance
has publication info: NP55998.RAS57evhd7XKASoDC6JK-cnSxWCHB0GsgJYvI44VgVjTs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55998.RAS57evhd7XKASoDC6JK-cnSxWCHB0GsgJYvI44VgVjTs130 assertion
type: Assertion
description: [Our results suggested that the IL-8 -251 T>A polymorphism may be a relevant host susceptibility factor for bladder carcinoma development and may influence outcome after BCG immunotherapy. Similarly, NF-kappaB ATTG polymorphism may also modify risk-free survival of BCG-treated patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20470938
was generated by: ECO_0000203

NP55999.RAcHDn-czaNZ7NLxqIxtAYI991vjyxmsv67glwUXIkBUs
has assertion: NP55999.RAcHDn-czaNZ7NLxqIxtAYI991vjyxmsv67glwUXIkBUs130 assertion
has provenance: NP55999.RAcHDn-czaNZ7NLxqIxtAYI991vjyxmsv67glwUXIkBUs130 provenance
has publication info: NP55999.RAcHDn-czaNZ7NLxqIxtAYI991vjyxmsv67glwUXIkBUs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP55999.RAcHDn-czaNZ7NLxqIxtAYI991vjyxmsv67glwUXIkBUs130 assertion
type: Assertion
description: [Lack of association between pro-inflammatory cytokine (IL-6, IL-8 and TNF-alpha) gene polymorphisms and Graves' disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16313297
was generated by: ECO_0000203

NP56002.RAajS0bzdetCUmmpBmvwFacPoaFred-CkUgsrUbZS-pa4
has assertion: NP56002.RAajS0bzdetCUmmpBmvwFacPoaFred-CkUgsrUbZS-pa4130 assertion
has provenance: NP56002.RAajS0bzdetCUmmpBmvwFacPoaFred-CkUgsrUbZS-pa4130 provenance
has publication info: NP56002.RAajS0bzdetCUmmpBmvwFacPoaFred-CkUgsrUbZS-pa4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56002.RAajS0bzdetCUmmpBmvwFacPoaFred-CkUgsrUbZS-pa4130 assertion
type: Assertion
description: [This observation draws attention to the possible importance of IL-8 polymorphism as a genetic predisposing factor in the pathomechanism of H. pylori-induced duodenal ulcer disease, and to the relative protection from duodenal ulcer disease that is associated with the TT genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15627645
was generated by: ECO_0000203

NP56010.RAUkXcSqN9vsrFIiJKkPfifpHcmH-KbuEVQuxF2tgOoC0
has assertion: NP56010.RAUkXcSqN9vsrFIiJKkPfifpHcmH-KbuEVQuxF2tgOoC0130 assertion
has provenance: NP56010.RAUkXcSqN9vsrFIiJKkPfifpHcmH-KbuEVQuxF2tgOoC0130 provenance
has publication info: NP56010.RAUkXcSqN9vsrFIiJKkPfifpHcmH-KbuEVQuxF2tgOoC0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56010.RAUkXcSqN9vsrFIiJKkPfifpHcmH-KbuEVQuxF2tgOoC0130 assertion
type: Assertion
description: [The association between common SNPs in immunologic response-related genes and CRC is reported in the present study. Apart from shedding light on the mechanisms of malignancy initiation and progression, SNPs may improve appropriate screening for sub-populations at risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16937502
was generated by: ECO_0000203

NP56011.RAYeN9F2tREQQH5PmH73gKTLfl5bE 4zzN7tK tAz2k6c
has assertion: NP56011.RAYeN9F2tREQQH5PmH73gKTLfl5bE 4zzN7tK tAz2k6c130 assertion
has provenance: NP56011.RAYeN9F2tREQQH5PmH73gKTLfl5bE 4zzN7tK tAz2k6c130 provenance
has publication info: NP56011.RAYeN9F2tREQQH5PmH73gKTLfl5bE 4zzN7tK tAz2k6c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56011.RAYeN9F2tREQQH5PmH73gKTLfl5bE 4zzN7tK tAz2k6c130 assertion
type: Assertion
description: [Cyclin D1 and epidermal growth factor polymorphisms associated with survival in patients with advanced colorectal cancer treated with Cetuximab.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16788380
was generated by: ECO_0000203

NP56015.RAYMar-H1O1YGOHCciWMI4mO7Ucl H-3uPtYhBOChbH3A
has assertion: NP56015.RAYMar-H1O1YGOHCciWMI4mO7Ucl H-3uPtYhBOChbH3A130 assertion
has provenance: NP56015.RAYMar-H1O1YGOHCciWMI4mO7Ucl H-3uPtYhBOChbH3A130 provenance
has publication info: NP56015.RAYMar-H1O1YGOHCciWMI4mO7Ucl H-3uPtYhBOChbH3A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56015.RAYMar-H1O1YGOHCciWMI4mO7Ucl H-3uPtYhBOChbH3A130 assertion
type: Assertion
description: [The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20437058
was generated by: ECO_0000203

NP56016.RAQzJaxGwjPeSeq55QpkEaEPJEXuxz DRm6-daVwo85g
has assertion: NP56016.RAQzJaxGwjPeSeq55QpkEaEPJEXuxz DRm6-daVwo85g130 assertion
has provenance: NP56016.RAQzJaxGwjPeSeq55QpkEaEPJEXuxz DRm6-daVwo85g130 provenance
has publication info: NP56016.RAQzJaxGwjPeSeq55QpkEaEPJEXuxz DRm6-daVwo85g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56016.RAQzJaxGwjPeSeq55QpkEaEPJEXuxz DRm6-daVwo85g130 assertion
type: Assertion
description: [Association of respiratory syncytial virus bronchiolitis with the interleukin 8 gene region in UK families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11083887
was generated by: ECO_0000203

NP56018.RAZsOjIvtNOjf1QdFKT6gTMJynU3bQTlhd3NyBZ8fsSQw
has assertion: NP56018.RAZsOjIvtNOjf1QdFKT6gTMJynU3bQTlhd3NyBZ8fsSQw130 assertion
has provenance: NP56018.RAZsOjIvtNOjf1QdFKT6gTMJynU3bQTlhd3NyBZ8fsSQw130 provenance
has publication info: NP56018.RAZsOjIvtNOjf1QdFKT6gTMJynU3bQTlhd3NyBZ8fsSQw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56018.RAZsOjIvtNOjf1QdFKT6gTMJynU3bQTlhd3NyBZ8fsSQw130 assertion
type: Assertion
description: [The genetic association between CCR3 polymorphisms and the number of circulating eosinophils was revealed as a novel finding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17983872
was generated by: ECO_0000203

NP56025.RAZOZzPWDDonoAvVj7thVcLs7d13CI-mX W-9c8BxEPyc
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has provenance: NP56025.RAZOZzPWDDonoAvVj7thVcLs7d13CI-mX W-9c8BxEPyc130 provenance
has publication info: NP56025.RAZOZzPWDDonoAvVj7thVcLs7d13CI-mX W-9c8BxEPyc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56025.RAZOZzPWDDonoAvVj7thVcLs7d13CI-mX W-9c8BxEPyc130 assertion
type: Assertion
description: [We found that the rs2522411SNP and the haplotype T-A in the IL-5 gene and the serum IL-5 levels were strongly associated with the allergic type of AD, but not with the nonallergic type of AD. The association of the rs6771148SNP and the haplotype T-C-T in the IL5RA gene with the blood eosinophil counts and the serum ECP levels indicates that the IL5RA gene ha]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17620072
was generated by: ECO_0000203

NP56026.RAY7DO5Dh7t6EqOpNqPoskYmIqhQeaD76ppYpDWhJU1ZA
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has provenance: NP56026.RAY7DO5Dh7t6EqOpNqPoskYmIqhQeaD76ppYpDWhJU1ZA130 provenance
has publication info: NP56026.RAY7DO5Dh7t6EqOpNqPoskYmIqhQeaD76ppYpDWhJU1ZA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56026.RAY7DO5Dh7t6EqOpNqPoskYmIqhQeaD76ppYpDWhJU1ZA130 assertion
type: Assertion
description: [ The cytokine gene polymorphisms studied here do not appear to influence IBD susceptibility. There does, however, appear to be an influence on disease phenotype, particularly on CD site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15842590
was generated by: ECO_0000203

NP56027.RAftT5URnolffH vnGMHy7UpLbzLAbgo1KtMNTG4-UXco
has assertion: NP56027.RAftT5URnolffH vnGMHy7UpLbzLAbgo1KtMNTG4-UXco130 assertion
has provenance: NP56027.RAftT5URnolffH vnGMHy7UpLbzLAbgo1KtMNTG4-UXco130 provenance
has publication info: NP56027.RAftT5URnolffH vnGMHy7UpLbzLAbgo1KtMNTG4-UXco130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56027.RAftT5URnolffH vnGMHy7UpLbzLAbgo1KtMNTG4-UXco130 assertion
type: Assertion
description: [Genetic approaches to the investigation of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11981324
was generated by: ECO_0000203

NP56037.RAeN3BbEbDp7 peTIDRCAR6V91oTTgMRNvgUuh7MeC8qE
has assertion: NP56037.RAeN3BbEbDp7 peTIDRCAR6V91oTTgMRNvgUuh7MeC8qE130 assertion
has provenance: NP56037.RAeN3BbEbDp7 peTIDRCAR6V91oTTgMRNvgUuh7MeC8qE130 provenance
has publication info: NP56037.RAeN3BbEbDp7 peTIDRCAR6V91oTTgMRNvgUuh7MeC8qE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56037.RAeN3BbEbDp7 peTIDRCAR6V91oTTgMRNvgUuh7MeC8qE130 assertion
type: Assertion
description: [Molecular analysis of adrenergic receptor genes and interleukin-4/interleukin-4 receptor genes in patients with interstitial cystitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12442007
was generated by: ECO_0000203

NP56045.RAUksXADxnfrYuYAII9Od2b97m2YJBYsZXzg1U43tq5Jo
has assertion: NP56045.RAUksXADxnfrYuYAII9Od2b97m2YJBYsZXzg1U43tq5Jo130 assertion
has provenance: NP56045.RAUksXADxnfrYuYAII9Od2b97m2YJBYsZXzg1U43tq5Jo130 provenance
has publication info: NP56045.RAUksXADxnfrYuYAII9Od2b97m2YJBYsZXzg1U43tq5Jo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56045.RAUksXADxnfrYuYAII9Od2b97m2YJBYsZXzg1U43tq5Jo130 assertion
type: Assertion
description: [The mutant R576 allele of IL-4R may be one of the candidate genes for susceptibility to asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16613701
was generated by: ECO_0000203

NP56046.RAYKbcJtusx4SQbLRCE40c4jHkupAfce KpRNaZGGCeAY
has assertion: NP56046.RAYKbcJtusx4SQbLRCE40c4jHkupAfce KpRNaZGGCeAY130 assertion
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has publication info: NP56046.RAYKbcJtusx4SQbLRCE40c4jHkupAfce KpRNaZGGCeAY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56046.RAYKbcJtusx4SQbLRCE40c4jHkupAfce KpRNaZGGCeAY130 assertion
type: Assertion
description: [Polymorphisms in the interleukin-4 receptor alpha chain: association with traits of allergy and asthma in an admixed population in Hawaii.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14984008
was generated by: ECO_0000203

NP56053.RAaxRL 8wY89uZ0wt0jAyjocFfLc7BrCXMMQT0D22MIzQ
has assertion: NP56053.RAaxRL 8wY89uZ0wt0jAyjocFfLc7BrCXMMQT0D22MIzQ130 assertion
has provenance: NP56053.RAaxRL 8wY89uZ0wt0jAyjocFfLc7BrCXMMQT0D22MIzQ130 provenance
has publication info: NP56053.RAaxRL 8wY89uZ0wt0jAyjocFfLc7BrCXMMQT0D22MIzQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56053.RAaxRL 8wY89uZ0wt0jAyjocFfLc7BrCXMMQT0D22MIzQ130 assertion
type: Assertion
description: [Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10677312
was generated by: ECO_0000203

NP56055.RAZ9FWoFzbv8XdN4zkMxcbUbvZ6O9IPq6Pe2yZIhpu h8
has assertion: NP56055.RAZ9FWoFzbv8XdN4zkMxcbUbvZ6O9IPq6Pe2yZIhpu h8130 assertion
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type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56055.RAZ9FWoFzbv8XdN4zkMxcbUbvZ6O9IPq6Pe2yZIhpu h8130 assertion
type: Assertion
description: [Associations with IL6 -174 variants suggest that the C/C genotype has a protective effect (OR=0.13) while carriers of the G allele are more susceptible (OR=7.66) to EPF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15566952
was generated by: ECO_0000203

NP56063.RAZnDfhBdFHJFgAJj0wWgGuTYQmcB41MPtJ1xUdx9SN-Y
has assertion: NP56063.RAZnDfhBdFHJFgAJj0wWgGuTYQmcB41MPtJ1xUdx9SN-Y130 assertion
has provenance: NP56063.RAZnDfhBdFHJFgAJj0wWgGuTYQmcB41MPtJ1xUdx9SN-Y130 provenance
has publication info: NP56063.RAZnDfhBdFHJFgAJj0wWgGuTYQmcB41MPtJ1xUdx9SN-Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56063.RAZnDfhBdFHJFgAJj0wWgGuTYQmcB41MPtJ1xUdx9SN-Y130 assertion
type: Assertion
description: [RGMA and IL21R and their pathways are crucial in MS pathogenesis and warrant further studies as potential biomarkers and therapeutic targets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20072140
was generated by: ECO_0000203

NP56064.RAUAH5w1RlK yj2EdJ8tRyEjoibmlZiSDAZthec3NvnP0
has assertion: NP56064.RAUAH5w1RlK yj2EdJ8tRyEjoibmlZiSDAZthec3NvnP0130 assertion
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has publication info: NP56064.RAUAH5w1RlK yj2EdJ8tRyEjoibmlZiSDAZthec3NvnP0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56064.RAUAH5w1RlK yj2EdJ8tRyEjoibmlZiSDAZthec3NvnP0130 assertion
type: Assertion
description: [Analysis of multiple candidate genes in association with phenotypes of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20378664
was generated by: ECO_0000203

NP56072.RAXCiEvFoZetLjrp6YOmDTEsW3K0uPr5figi06IERWcPo
has assertion: NP56072.RAXCiEvFoZetLjrp6YOmDTEsW3K0uPr5figi06IERWcPo130 assertion
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has publication info: NP56072.RAXCiEvFoZetLjrp6YOmDTEsW3K0uPr5figi06IERWcPo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
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authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56072.RAXCiEvFoZetLjrp6YOmDTEsW3K0uPr5figi06IERWcPo130 assertion
type: Assertion
description: [The results indicate that these variants are not significant genetic determinants of IBD, and that the IL4R gene is unlikely to be IBD1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10663555
was generated by: ECO_0000203

NP56074.RAcXgDKL-gQHC851aj7KvvmWJ258vXdNQFfTsl4C22sNk
has assertion: NP56074.RAcXgDKL-gQHC851aj7KvvmWJ258vXdNQFfTsl4C22sNk130 assertion
has provenance: NP56074.RAcXgDKL-gQHC851aj7KvvmWJ258vXdNQFfTsl4C22sNk130 provenance
has publication info: NP56074.RAcXgDKL-gQHC851aj7KvvmWJ258vXdNQFfTsl4C22sNk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56074.RAcXgDKL-gQHC851aj7KvvmWJ258vXdNQFfTsl4C22sNk130 assertion
type: Assertion
description: [Alpha-1-antitrypsin (PI) and vitamin-D binding globulin (GC) phenotypes in rheumatoid arthritis: absence of an association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/2786461
was generated by: ECO_0000203

NP56079.RAb569cesM SHhDjhD7-103PuEoC0r9usdy CHREVyzu0
has assertion: NP56079.RAb569cesM SHhDjhD7-103PuEoC0r9usdy CHREVyzu0130 assertion
has provenance: NP56079.RAb569cesM SHhDjhD7-103PuEoC0r9usdy CHREVyzu0130 provenance
has publication info: NP56079.RAb569cesM SHhDjhD7-103PuEoC0r9usdy CHREVyzu0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
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authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56079.RAb569cesM SHhDjhD7-103PuEoC0r9usdy CHREVyzu0130 assertion
type: Assertion
description: [During analysis of role of allelic polymorphism of IL-4 genes in predisposition to hepatitis C development it is necessary to consider not only presence of allelic variants of promoter regions of the IL-4 genes, but also the polymorphism of genes coding molecules binding with this cytokine on target cells membranes and in its soluble form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17523428
was generated by: ECO_0000203

NP56080.RAYHrTl5hPH09jme4xpEttVvzIPpYvDFw9x3FInxa6Jp0
has assertion: NP56080.RAYHrTl5hPH09jme4xpEttVvzIPpYvDFw9x3FInxa6Jp0130 assertion
has provenance: NP56080.RAYHrTl5hPH09jme4xpEttVvzIPpYvDFw9x3FInxa6Jp0130 provenance
has publication info: NP56080.RAYHrTl5hPH09jme4xpEttVvzIPpYvDFw9x3FInxa6Jp0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56080.RAYHrTl5hPH09jme4xpEttVvzIPpYvDFw9x3FInxa6Jp0130 assertion
type: Assertion
description: [Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12082592
was generated by: ECO_0000203

NP56099.RAWZxIqTiK3yIgOf7XxKKUmmkU-o7IofmzcUJTooRrk80
has assertion: NP56099.RAWZxIqTiK3yIgOf7XxKKUmmkU-o7IofmzcUJTooRrk80130 assertion
has provenance: NP56099.RAWZxIqTiK3yIgOf7XxKKUmmkU-o7IofmzcUJTooRrk80130 provenance
has publication info: NP56099.RAWZxIqTiK3yIgOf7XxKKUmmkU-o7IofmzcUJTooRrk80130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56099.RAWZxIqTiK3yIgOf7XxKKUmmkU-o7IofmzcUJTooRrk80130 assertion
type: Assertion
description: [Impact of the IL-4 -590 C/T transition on the levels of Plasmodium falciparum specific IgE, IgG, IgG subclasses and total IgE in two sympatric ethnic groups living in Mali.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19409508
was generated by: ECO_0000203

NP56111.RAWV8w42aQafU1-H5MtB5STp44GS5-TEDAeP5SFEmKTec
has assertion: NP56111.RAWV8w42aQafU1-H5MtB5STp44GS5-TEDAeP5SFEmKTec130 assertion
has provenance: NP56111.RAWV8w42aQafU1-H5MtB5STp44GS5-TEDAeP5SFEmKTec130 provenance
has publication info: NP56111.RAWV8w42aQafU1-H5MtB5STp44GS5-TEDAeP5SFEmKTec130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56111.RAWV8w42aQafU1-H5MtB5STp44GS5-TEDAeP5SFEmKTec130 assertion
type: Assertion
description: [Polymorphism in the promoter of the IL-4 gene is associated with asthma and is a disease modifier in terms of the severity of AHR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17207024
was generated by: ECO_0000203

NP56116.RAQhAOh5elPgtU7hGe2YUqcN8SMdeWnBySYotrDL9QHo4
has assertion: NP56116.RAQhAOh5elPgtU7hGe2YUqcN8SMdeWnBySYotrDL9QHo4130 assertion
has provenance: NP56116.RAQhAOh5elPgtU7hGe2YUqcN8SMdeWnBySYotrDL9QHo4130 provenance
has publication info: NP56116.RAQhAOh5elPgtU7hGe2YUqcN8SMdeWnBySYotrDL9QHo4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56116.RAQhAOh5elPgtU7hGe2YUqcN8SMdeWnBySYotrDL9QHo4130 assertion
type: Assertion
description: [ Variants related to decreased anti-inflammatory cytokine production may lower risk of SGA. Furthermore, the same mechanism that protects against SGA might increase risk of spontaneous preterm birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15951665
was generated by: ECO_0000203

NP56119.RAfRJ9oFg0g5pdAWL2ayKyMXNya18OFUs4xdzuTiyw8-w
has assertion: NP56119.RAfRJ9oFg0g5pdAWL2ayKyMXNya18OFUs4xdzuTiyw8-w130 assertion
has provenance: NP56119.RAfRJ9oFg0g5pdAWL2ayKyMXNya18OFUs4xdzuTiyw8-w130 provenance
has publication info: NP56119.RAfRJ9oFg0g5pdAWL2ayKyMXNya18OFUs4xdzuTiyw8-w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56119.RAfRJ9oFg0g5pdAWL2ayKyMXNya18OFUs4xdzuTiyw8-w130 assertion
type: Assertion
description: [When UC patients were divided into ANCA positive and negative groups, it was found that there was significant difference in the gene frequencies of allele RP1, RP2 of IL-4 between two groups (63.7% vs 83.3%, 36.3% vs 16.7%, P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12133437
was generated by: ECO_0000203

NP56120.RAaSAQXWTuZjXwlNNF49d2unsKKb69UJqG4 7CyY0DyIY
has assertion: NP56120.RAaSAQXWTuZjXwlNNF49d2unsKKb69UJqG4 7CyY0DyIY130 assertion
has provenance: NP56120.RAaSAQXWTuZjXwlNNF49d2unsKKb69UJqG4 7CyY0DyIY130 provenance
has publication info: NP56120.RAaSAQXWTuZjXwlNNF49d2unsKKb69UJqG4 7CyY0DyIY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56120.RAaSAQXWTuZjXwlNNF49d2unsKKb69UJqG4 7CyY0DyIY130 assertion
type: Assertion
description: [ These data suggest that IL-4, IL-13 and IFN-gamma play an important roles in penicillins allergy. The IL-4RalphaQ576R polymorphism may involve in the development of penicillins allergy, and through modulating specific serum IgE levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15969687
was generated by: ECO_0000203

NP56122.RATIav0F3HH28QhlovlEdpcovaJbbP3CrvNc K3bKI4yQ
has assertion: NP56122.RATIav0F3HH28QhlovlEdpcovaJbbP3CrvNc K3bKI4yQ130 assertion
has provenance: NP56122.RATIav0F3HH28QhlovlEdpcovaJbbP3CrvNc K3bKI4yQ130 provenance
has publication info: NP56122.RATIav0F3HH28QhlovlEdpcovaJbbP3CrvNc K3bKI4yQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56122.RATIav0F3HH28QhlovlEdpcovaJbbP3CrvNc K3bKI4yQ130 assertion
type: Assertion
description: [ These findings not only suggested that variants in the IL4, IL13, and IL4RA genes play an important role in controlling specific IgE response but also strengthened our understanding of gene-gene and gene-environment interaction on the development of specific sensitization in this study population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15007352
was generated by: ECO_0000203

NP56126.RAevWoPxbjefiUqdXOdOlf9L52gTdpluqO5hjdCXABSeE
has assertion: NP56126.RAevWoPxbjefiUqdXOdOlf9L52gTdpluqO5hjdCXABSeE130 assertion
has provenance: NP56126.RAevWoPxbjefiUqdXOdOlf9L52gTdpluqO5hjdCXABSeE130 provenance
has publication info: NP56126.RAevWoPxbjefiUqdXOdOlf9L52gTdpluqO5hjdCXABSeE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56126.RAevWoPxbjefiUqdXOdOlf9L52gTdpluqO5hjdCXABSeE130 assertion
type: Assertion
description: [Genome-wide association scan yields new insights into the immunopathogenesis of psoriasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19262574
was generated by: ECO_0000203

NP56130.RAUidGSkYcBKsUygfOuDKMzVjMSuJYXTA41W e9Es7V98
has assertion: NP56130.RAUidGSkYcBKsUygfOuDKMzVjMSuJYXTA41W e9Es7V98130 assertion
has provenance: NP56130.RAUidGSkYcBKsUygfOuDKMzVjMSuJYXTA41W e9Es7V98130 provenance
has publication info: NP56130.RAUidGSkYcBKsUygfOuDKMzVjMSuJYXTA41W e9Es7V98130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56130.RAUidGSkYcBKsUygfOuDKMzVjMSuJYXTA41W e9Es7V98130 assertion
type: Assertion
description: [The association between GD and the following polymorphisms in anti-inflammatory cytokines was studied in 107 patients with GD and 140 healthy controls: IL-4 (-1098T/G, -590T/C, -33C/T), IL-10 (-1082A/G, -819C/T, -592C/A) and TGF-beta (+869T/C, +915G/C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19882211
was generated by: ECO_0000203

NP56140.RASyI3LSnT sAHq3t tad452amBtVNS6Kg nTNlvcr7p4
has assertion: NP56140.RASyI3LSnT sAHq3t tad452amBtVNS6Kg nTNlvcr7p4130 assertion
has provenance: NP56140.RASyI3LSnT sAHq3t tad452amBtVNS6Kg nTNlvcr7p4130 provenance
has publication info: NP56140.RASyI3LSnT sAHq3t tad452amBtVNS6Kg nTNlvcr7p4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56140.RASyI3LSnT sAHq3t tad452amBtVNS6Kg nTNlvcr7p4130 assertion
type: Assertion
description: [ The results suggest that IL-4 VNTR B1B1 genotype might be a predictor for the frequent relapse in childhood SSNS in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16053729
was generated by: ECO_0000203

NP56141.RAZ7Z4Rn4rzhATtP7zPz1gsdooI PeN-i3AFMAnpafE4
has assertion: NP56141.RAZ7Z4Rn4rzhATtP7zPz1gsdooI PeN-i3AFMAnpafE4130 assertion
has provenance: NP56141.RAZ7Z4Rn4rzhATtP7zPz1gsdooI PeN-i3AFMAnpafE4130 provenance
has publication info: NP56141.RAZ7Z4Rn4rzhATtP7zPz1gsdooI PeN-i3AFMAnpafE4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56141.RAZ7Z4Rn4rzhATtP7zPz1gsdooI PeN-i3AFMAnpafE4130 assertion
type: Assertion
description: [We could not confirm the previously reported association between carriage of I3(709)*allele-2 and older age of onset. However, we found a trend for association between the homozygous state for this allele and older age of onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12667657
was generated by: ECO_0000203

NP56142.RAaDC2CT2l4q0bXbYerhKNG1tJ1Ox zx3woP44oezUHy0
has assertion: NP56142.RAaDC2CT2l4q0bXbYerhKNG1tJ1Ox zx3woP44oezUHy0130 assertion
has provenance: NP56142.RAaDC2CT2l4q0bXbYerhKNG1tJ1Ox zx3woP44oezUHy0130 provenance
has publication info: NP56142.RAaDC2CT2l4q0bXbYerhKNG1tJ1Ox zx3woP44oezUHy0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56142.RAaDC2CT2l4q0bXbYerhKNG1tJ1Ox zx3woP44oezUHy0130 assertion
type: Assertion
description: [Since interleukin (IL)-4 gene polymorphisms have been associated with immune-mediated diseases, we have analysed the relationship between a variable number of tandem repeat polymorphism of the IL-4 gene and clinical and physiological features of 256 sporadic MS patients and 146 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9184650
was generated by: ECO_0000203

NP56148.RAZnQ12cDz8qYs7kRRHC5okdud8xYmA49Y4abjoQo7W8Y
has assertion: NP56148.RAZnQ12cDz8qYs7kRRHC5okdud8xYmA49Y4abjoQo7W8Y130 assertion
has provenance: NP56148.RAZnQ12cDz8qYs7kRRHC5okdud8xYmA49Y4abjoQo7W8Y130 provenance
has publication info: NP56148.RAZnQ12cDz8qYs7kRRHC5okdud8xYmA49Y4abjoQo7W8Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56148.RAZnQ12cDz8qYs7kRRHC5okdud8xYmA49Y4abjoQo7W8Y130 assertion
type: Assertion
description: [Association of interleukin-4 receptor and interleukin-4 promoter gene polymorphisms with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10366128
was generated by: ECO_0000203

NP56151.RAeOn8TrLejE95HHx2P9xGclDFIz 0N 3cIr1M zKScS0
has assertion: NP56151.RAeOn8TrLejE95HHx2P9xGclDFIz 0N 3cIr1M zKScS0130 assertion
has provenance: NP56151.RAeOn8TrLejE95HHx2P9xGclDFIz 0N 3cIr1M zKScS0130 provenance
has publication info: NP56151.RAeOn8TrLejE95HHx2P9xGclDFIz 0N 3cIr1M zKScS0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56151.RAeOn8TrLejE95HHx2P9xGclDFIz 0N 3cIr1M zKScS0130 assertion
type: Assertion
description: [Association with alleles resulting in high IL-4 transcription and enhanced signalling activity suggests that IL-4 may have a role in the pathogenesis of Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11294568
was generated by: ECO_0000203

NP56152.RAWRbGyVkrdsRb9u-KELQRMOoWGTaC0Sam3kvZZCOIes8
has assertion: NP56152.RAWRbGyVkrdsRb9u-KELQRMOoWGTaC0Sam3kvZZCOIes8130 assertion
has provenance: NP56152.RAWRbGyVkrdsRb9u-KELQRMOoWGTaC0Sam3kvZZCOIes8130 provenance
has publication info: NP56152.RAWRbGyVkrdsRb9u-KELQRMOoWGTaC0Sam3kvZZCOIes8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56152.RAWRbGyVkrdsRb9u-KELQRMOoWGTaC0Sam3kvZZCOIes8130 assertion
type: Assertion
description: [Thus, IL-13 -1055T may show resistance to severe malaria through the alteration of IL-13 production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14551608
was generated by: ECO_0000203

NP56164.RASzlO6XK8u48Q6TIzaL4NKe41ARKb5RXMv0PUAnIuB5s
has assertion: NP56164.RASzlO6XK8u48Q6TIzaL4NKe41ARKb5RXMv0PUAnIuB5s130 assertion
has provenance: NP56164.RASzlO6XK8u48Q6TIzaL4NKe41ARKb5RXMv0PUAnIuB5s130 provenance
has publication info: NP56164.RASzlO6XK8u48Q6TIzaL4NKe41ARKb5RXMv0PUAnIuB5s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56164.RASzlO6XK8u48Q6TIzaL4NKe41ARKb5RXMv0PUAnIuB5s130 assertion
type: Assertion
description: [ Our study showed association with JIA for the IL-4 -1098 T/G polymorphism. It also underlines the genetic contribution of IL-1 polymorphisms to the pathogenesis of JIA, as another polymorphism within the IL-1beta may influence the risk of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15170937
was generated by: ECO_0000203

NP56165.RAX33jmRCVGs4tIl-bz9iz Z8NKMG2nNAvOKrsHckGaT0
has assertion: NP56165.RAX33jmRCVGs4tIl-bz9iz Z8NKMG2nNAvOKrsHckGaT0130 assertion
has provenance: NP56165.RAX33jmRCVGs4tIl-bz9iz Z8NKMG2nNAvOKrsHckGaT0130 provenance
has publication info: NP56165.RAX33jmRCVGs4tIl-bz9iz Z8NKMG2nNAvOKrsHckGaT0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56165.RAX33jmRCVGs4tIl-bz9iz Z8NKMG2nNAvOKrsHckGaT0130 assertion
type: Assertion
description: [Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16389181
was generated by: ECO_0000203

NP56173.RAd24r1z0TaHuEzSjCEttU5mIR8pELcw7eZZDtBkQwg4E
has assertion: NP56173.RAd24r1z0TaHuEzSjCEttU5mIR8pELcw7eZZDtBkQwg4E130 assertion
has provenance: NP56173.RAd24r1z0TaHuEzSjCEttU5mIR8pELcw7eZZDtBkQwg4E130 provenance
has publication info: NP56173.RAd24r1z0TaHuEzSjCEttU5mIR8pELcw7eZZDtBkQwg4E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56173.RAd24r1z0TaHuEzSjCEttU5mIR8pELcw7eZZDtBkQwg4E130 assertion
type: Assertion
description: [Association study of interleukin 2 (IL2) and IL4 with schizophrenia in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18574615
was generated by: ECO_0000203

NP56203.RAWEbBhWJpnW-4Ky-E vwzIDnvWrT7Md7735mc 7CYfVI
has assertion: NP56203.RAWEbBhWJpnW-4Ky-E vwzIDnvWrT7Md7735mc 7CYfVI130 assertion
has provenance: NP56203.RAWEbBhWJpnW-4Ky-E vwzIDnvWrT7Md7735mc 7CYfVI130 provenance
has publication info: NP56203.RAWEbBhWJpnW-4Ky-E vwzIDnvWrT7Md7735mc 7CYfVI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56203.RAWEbBhWJpnW-4Ky-E vwzIDnvWrT7Md7735mc 7CYfVI130 assertion
type: Assertion
description: [We examined the association between malignant lymphoma risk and the polymorphisms of the IL-1 gene family IL-1B -31 C/T, IL-1A -889 C/T, and IL-1RN 86-bp variable number of terminal repeat (VNTR) and myeloperoxidase (MPO -463 G/A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11423389
was generated by: ECO_0000203

NP56211.RAbALwE1EiRq1kPtmBptM9XZGJ1mtjFMw uKoyqFggByo
has assertion: NP56211.RAbALwE1EiRq1kPtmBptM9XZGJ1mtjFMw uKoyqFggByo130 assertion
has provenance: NP56211.RAbALwE1EiRq1kPtmBptM9XZGJ1mtjFMw uKoyqFggByo130 provenance
has publication info: NP56211.RAbALwE1EiRq1kPtmBptM9XZGJ1mtjFMw uKoyqFggByo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56211.RAbALwE1EiRq1kPtmBptM9XZGJ1mtjFMw uKoyqFggByo130 assertion
type: Assertion
description: [In conclusion, no association of the IL1B C(minus sign?31)T with HT was found, whereas combined frequency of the minor alleles of the IL1RN polymorphism was increased in the HT cohort studied]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11840488
was generated by: ECO_0000203

NP56221.RASbDOc LkZ7ULqBkMmYjrs8gHFh5f0RuEyxdrQG m8xE
has assertion: NP56221.RASbDOc LkZ7ULqBkMmYjrs8gHFh5f0RuEyxdrQG m8xE130 assertion
has provenance: NP56221.RASbDOc LkZ7ULqBkMmYjrs8gHFh5f0RuEyxdrQG m8xE130 provenance
has publication info: NP56221.RASbDOc LkZ7ULqBkMmYjrs8gHFh5f0RuEyxdrQG m8xE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56221.RASbDOc LkZ7ULqBkMmYjrs8gHFh5f0RuEyxdrQG m8xE130 assertion
type: Assertion
description: [ The single nucleotide polymorphism of IL-1B-31C may contribute to the development of the gastric adenocarcinoma in the H. pylori-positive population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15266130
was generated by: ECO_0000203

NP56223.RAaaEga 3PihlUuGCccDArNC0FLusK6ENMUrDA3SVxVr8
has assertion: NP56223.RAaaEga 3PihlUuGCccDArNC0FLusK6ENMUrDA3SVxVr8130 assertion
has provenance: NP56223.RAaaEga 3PihlUuGCccDArNC0FLusK6ENMUrDA3SVxVr8130 provenance
has publication info: NP56223.RAaaEga 3PihlUuGCccDArNC0FLusK6ENMUrDA3SVxVr8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56223.RAaaEga 3PihlUuGCccDArNC0FLusK6ENMUrDA3SVxVr8130 assertion
type: Assertion
description: [Allele 2 of the interleukin-1 receptor antagonist gene is associated with early gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15570075
was generated by: ECO_0000203

NP56226.RAekNhe05D4ld3TlHJ7dLDjGQzXVUNEpmVFHMndeYrZQM
has assertion: NP56226.RAekNhe05D4ld3TlHJ7dLDjGQzXVUNEpmVFHMndeYrZQM130 assertion
has provenance: NP56226.RAekNhe05D4ld3TlHJ7dLDjGQzXVUNEpmVFHMndeYrZQM130 provenance
has publication info: NP56226.RAekNhe05D4ld3TlHJ7dLDjGQzXVUNEpmVFHMndeYrZQM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56226.RAekNhe05D4ld3TlHJ7dLDjGQzXVUNEpmVFHMndeYrZQM130 assertion
type: Assertion
description: [According to their random-Odds Ratios, individuals carrying one of the IL-1RN *2, IL-1beta -511T variant alleles or homozygotes for MTHFR 677T are significantly at higher risk of gastric cancer than those with the wild type homozygote genotypes, showing high PARs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19506726
was generated by: ECO_0000203

NP56227.RAdaqRZcAXYSEq8g4XaQAwuy ODRtg7kbFk3 RqLD76CI
has assertion: NP56227.RAdaqRZcAXYSEq8g4XaQAwuy ODRtg7kbFk3 RqLD76CI130 assertion
has provenance: NP56227.RAdaqRZcAXYSEq8g4XaQAwuy ODRtg7kbFk3 RqLD76CI130 provenance
has publication info: NP56227.RAdaqRZcAXYSEq8g4XaQAwuy ODRtg7kbFk3 RqLD76CI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56227.RAdaqRZcAXYSEq8g4XaQAwuy ODRtg7kbFk3 RqLD76CI130 assertion
type: Assertion
description: [ Genetic variations in cytokine and DNA repair genes contribute to susceptibility to HBV-related HCC. Smoking increased such genetic susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16172101
was generated by: ECO_0000203

NP56228.RAT5WStw-AoSdUGYZ7eU2bt4GI97YqE5U0XK6HsNOaM6E
has assertion: NP56228.RAT5WStw-AoSdUGYZ7eU2bt4GI97YqE5U0XK6HsNOaM6E130 assertion
has provenance: NP56228.RAT5WStw-AoSdUGYZ7eU2bt4GI97YqE5U0XK6HsNOaM6E130 provenance
has publication info: NP56228.RAT5WStw-AoSdUGYZ7eU2bt4GI97YqE5U0XK6HsNOaM6E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56228.RAT5WStw-AoSdUGYZ7eU2bt4GI97YqE5U0XK6HsNOaM6E130 assertion
type: Assertion
description: [The genotype I/II for IL1-Ra and the frequency of allele II for IL1-Ra are associated with a higher susceptibility to KD, and thus may be useful markers for predicting the development of KD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15900570
was generated by: ECO_0000203

NP56237.RAQH4zzwJjaZVPs238fea4tNhnTt9nbiJkrUhpDIDk09w
has assertion: NP56237.RAQH4zzwJjaZVPs238fea4tNhnTt9nbiJkrUhpDIDk09w130 assertion
has provenance: NP56237.RAQH4zzwJjaZVPs238fea4tNhnTt9nbiJkrUhpDIDk09w130 provenance
has publication info: NP56237.RAQH4zzwJjaZVPs238fea4tNhnTt9nbiJkrUhpDIDk09w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56237.RAQH4zzwJjaZVPs238fea4tNhnTt9nbiJkrUhpDIDk09w130 assertion
type: Assertion
description: [A potential pharmacogenomic strategy for anticoagulant treatment in non-ST elevation acute coronary syndromes: the role of interleukin-1 receptor antagonist genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15670034
was generated by: ECO_0000203

NP56238.RAc1dFJcRZMdAwmHz-8hhG0NlFJhjDgb3-uHKsMPErYkc
has assertion: NP56238.RAc1dFJcRZMdAwmHz-8hhG0NlFJhjDgb3-uHKsMPErYkc130 assertion
has provenance: NP56238.RAc1dFJcRZMdAwmHz-8hhG0NlFJhjDgb3-uHKsMPErYkc130 provenance
has publication info: NP56238.RAc1dFJcRZMdAwmHz-8hhG0NlFJhjDgb3-uHKsMPErYkc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56238.RAc1dFJcRZMdAwmHz-8hhG0NlFJhjDgb3-uHKsMPErYkc130 assertion
type: Assertion
description: [The purpose of this study was to determine the relationship between IL-1 gene family polymorphisms (IL-1RN, IL-1B in positions -511 and +3953) and ACS in the Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18299273
was generated by: ECO_0000203

NP56241.RAeVyjNCd7sH5PH94dKdr3BA505DPoy9a4elRX9Vdb20M
has assertion: NP56241.RAeVyjNCd7sH5PH94dKdr3BA505DPoy9a4elRX9Vdb20M130 assertion
has provenance: NP56241.RAeVyjNCd7sH5PH94dKdr3BA505DPoy9a4elRX9Vdb20M130 provenance
has publication info: NP56241.RAeVyjNCd7sH5PH94dKdr3BA505DPoy9a4elRX9Vdb20M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56241.RAeVyjNCd7sH5PH94dKdr3BA505DPoy9a4elRX9Vdb20M130 assertion
type: Assertion
description: [Association of interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in Turkish children with atopic asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18926055
was generated by: ECO_0000203

NP56249.RAU Dd2lukIw-G6YCRRtf2VwrYJQmIJCNDInfFftso VQ
has assertion: NP56249.RAU Dd2lukIw-G6YCRRtf2VwrYJQmIJCNDInfFftso VQ130 assertion
has provenance: NP56249.RAU Dd2lukIw-G6YCRRtf2VwrYJQmIJCNDInfFftso VQ130 provenance
has publication info: NP56249.RAU Dd2lukIw-G6YCRRtf2VwrYJQmIJCNDInfFftso VQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56249.RAU Dd2lukIw-G6YCRRtf2VwrYJQmIJCNDInfFftso VQ130 assertion
type: Assertion
description: [Interleukin-1 receptor antagonist gene polymorphism in Japanese patients with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9041953
was generated by: ECO_0000203

NP56259.RAXA2UNlB3wFgNhHJPuqZOZZrPv1BaPUTO1TE AsGkIqQ
has assertion: NP56259.RAXA2UNlB3wFgNhHJPuqZOZZrPv1BaPUTO1TE AsGkIqQ130 assertion
has provenance: NP56259.RAXA2UNlB3wFgNhHJPuqZOZZrPv1BaPUTO1TE AsGkIqQ130 provenance
has publication info: NP56259.RAXA2UNlB3wFgNhHJPuqZOZZrPv1BaPUTO1TE AsGkIqQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56259.RAXA2UNlB3wFgNhHJPuqZOZZrPv1BaPUTO1TE AsGkIqQ130 assertion
type: Assertion
description: [Association between interleukin-1 receptor antagonist (IL-1ra) gene polymorphism and early and late-onset psoriasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9039327
was generated by: ECO_0000203

NP56261.RAbXT0LZS7OPLLy2filOQHCXGgaH5qstD RqLRxc09vVk
has assertion: NP56261.RAbXT0LZS7OPLLy2filOQHCXGgaH5qstD RqLRxc09vVk130 assertion
has provenance: NP56261.RAbXT0LZS7OPLLy2filOQHCXGgaH5qstD RqLRxc09vVk130 provenance
has publication info: NP56261.RAbXT0LZS7OPLLy2filOQHCXGgaH5qstD RqLRxc09vVk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56261.RAbXT0LZS7OPLLy2filOQHCXGgaH5qstD RqLRxc09vVk130 assertion
type: Assertion
description: [Our results suggest that IL-1ra polymorphisms are not associated with the development of IgAN in Japanese patients but the presence of IL1RN*2 may be associated with increased disease activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12138282
was generated by: ECO_0000203

NP56262.RAZFwepBHpFkXX4DTyuJIuddWH6MF9bhMFF1Ksw6oBliA
has assertion: NP56262.RAZFwepBHpFkXX4DTyuJIuddWH6MF9bhMFF1Ksw6oBliA130 assertion
has provenance: NP56262.RAZFwepBHpFkXX4DTyuJIuddWH6MF9bhMFF1Ksw6oBliA130 provenance
has publication info: NP56262.RAZFwepBHpFkXX4DTyuJIuddWH6MF9bhMFF1Ksw6oBliA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56262.RAZFwepBHpFkXX4DTyuJIuddWH6MF9bhMFF1Ksw6oBliA130 assertion
type: Assertion
description: [Interleukin-1 cluster gene polymorphisms in childhood IgA nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19280228
was generated by: ECO_0000203

NP56269.RAdl AOwWs2CUoze6F8hTIt9rjUMUVURr8CAbNE89aeJI
has assertion: NP56269.RAdl AOwWs2CUoze6F8hTIt9rjUMUVURr8CAbNE89aeJI130 assertion
has provenance: NP56269.RAdl AOwWs2CUoze6F8hTIt9rjUMUVURr8CAbNE89aeJI130 provenance
has publication info: NP56269.RAdl AOwWs2CUoze6F8hTIt9rjUMUVURr8CAbNE89aeJI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56269.RAdl AOwWs2CUoze6F8hTIt9rjUMUVURr8CAbNE89aeJI130 assertion
type: Assertion
description: [Our results suggest that these polymorphisms within IL1RN and IL1L1 themselves or a gene in linkage disequilibrium with IL1RN and IL1L1 predispose to the more severe forms of alopecia areata.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11841485
was generated by: ECO_0000203

NP56280.RAWAfcB-K3EVjy3RcoDWSbrxxQQ36v-BQV1A02VWgJpCw
has assertion: NP56280.RAWAfcB-K3EVjy3RcoDWSbrxxQQ36v-BQV1A02VWgJpCw130 assertion
has provenance: NP56280.RAWAfcB-K3EVjy3RcoDWSbrxxQQ36v-BQV1A02VWgJpCw130 provenance
has publication info: NP56280.RAWAfcB-K3EVjy3RcoDWSbrxxQQ36v-BQV1A02VWgJpCw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56280.RAWAfcB-K3EVjy3RcoDWSbrxxQQ36v-BQV1A02VWgJpCw130 assertion
type: Assertion
description: [Association of polymorphisms in CTLA-4, IL-1ra and IL-1beta genes with multiple sclerosis in Serbian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16769128
was generated by: ECO_0000203

NP56289.RAbubzXrbXyNLLN8gTqGI-FWNH7yyqtx8abGrleBL5Iag
has assertion: NP56289.RAbubzXrbXyNLLN8gTqGI-FWNH7yyqtx8abGrleBL5Iag130 assertion
has provenance: NP56289.RAbubzXrbXyNLLN8gTqGI-FWNH7yyqtx8abGrleBL5Iag130 provenance
has publication info: NP56289.RAbubzXrbXyNLLN8gTqGI-FWNH7yyqtx8abGrleBL5Iag130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56289.RAbubzXrbXyNLLN8gTqGI-FWNH7yyqtx8abGrleBL5Iag130 assertion
type: Assertion
description: [Interleukin-1 receptor antagonist gene polymorphism as a disease severity factor in systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/7945503
was generated by: ECO_0000203

NP56291.RAQU8aPOmMi2MxGumANgdsQyaz8xztDsBPwi01tnhDyDo
has assertion: NP56291.RAQU8aPOmMi2MxGumANgdsQyaz8xztDsBPwi01tnhDyDo130 assertion
has provenance: NP56291.RAQU8aPOmMi2MxGumANgdsQyaz8xztDsBPwi01tnhDyDo130 provenance
has publication info: NP56291.RAQU8aPOmMi2MxGumANgdsQyaz8xztDsBPwi01tnhDyDo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56291.RAQU8aPOmMi2MxGumANgdsQyaz8xztDsBPwi01tnhDyDo130 assertion
type: Assertion
description: [Although ours and other published data on different samples of Caucasian and non-Caucasian AD show a great heterogeneity in the frequencies of the IL-1alpha(-889), the IL-1beta(-511) and the IL-1Ra VNTR gene polymorphisms, we confirm the role of the IL-1alpha(-889) T/T genotype as a risk factor for sporadic AD, and show the presence of an allelic association between IL-1beta C and IL-1Ra 1 alleles in both the Italian and the USA groups, confirmed by the presence of significant levels of linkage disequilibrium between these two loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15653174
was generated by: ECO_0000203

NP56293.RAZqoJwVGSolxco52w9RqEnsMRKTXZcrHsENkUNawwmzg
has assertion: NP56293.RAZqoJwVGSolxco52w9RqEnsMRKTXZcrHsENkUNawwmzg130 assertion
has provenance: NP56293.RAZqoJwVGSolxco52w9RqEnsMRKTXZcrHsENkUNawwmzg130 provenance
has publication info: NP56293.RAZqoJwVGSolxco52w9RqEnsMRKTXZcrHsENkUNawwmzg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56293.RAZqoJwVGSolxco52w9RqEnsMRKTXZcrHsENkUNawwmzg130 assertion
type: Assertion
description: [Genetic approaches to the investigation of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11981324
was generated by: ECO_0000203

NP56313.RASRkclUVfyQRh 3skB3wkTl1cGCH6MDs lsUS4 E1q1I
has assertion: NP56313.RASRkclUVfyQRh 3skB3wkTl1cGCH6MDs lsUS4 E1q1I130 assertion
has provenance: NP56313.RASRkclUVfyQRh 3skB3wkTl1cGCH6MDs lsUS4 E1q1I130 provenance
has publication info: NP56313.RASRkclUVfyQRh 3skB3wkTl1cGCH6MDs lsUS4 E1q1I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56313.RASRkclUVfyQRh 3skB3wkTl1cGCH6MDs lsUS4 E1q1I130 assertion
type: Assertion
description: [Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19141999
was generated by: ECO_0000203

NP56318.RAWqYNRWUuE5pyAfgxtZBBDq7NUc-RjJVKi626xrLYCTE
has assertion: NP56318.RAWqYNRWUuE5pyAfgxtZBBDq7NUc-RjJVKi626xrLYCTE130 assertion
has provenance: NP56318.RAWqYNRWUuE5pyAfgxtZBBDq7NUc-RjJVKi626xrLYCTE130 provenance
has publication info: NP56318.RAWqYNRWUuE5pyAfgxtZBBDq7NUc-RjJVKi626xrLYCTE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56318.RAWqYNRWUuE5pyAfgxtZBBDq7NUc-RjJVKi626xrLYCTE130 assertion
type: Assertion
description: [The sorted genes allow us to draw novel hypotheses for future studies of HCV infection to ultimately identify bona fide genes and their variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15063762
was generated by: ECO_0000203

NP56325.RAXQfZiIs728lt5kBiHdE9cZKJHr roVdEbjP0urM3ZBY
has assertion: NP56325.RAXQfZiIs728lt5kBiHdE9cZKJHr roVdEbjP0urM3ZBY130 assertion
has provenance: NP56325.RAXQfZiIs728lt5kBiHdE9cZKJHr roVdEbjP0urM3ZBY130 provenance
has publication info: NP56325.RAXQfZiIs728lt5kBiHdE9cZKJHr roVdEbjP0urM3ZBY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56325.RAXQfZiIs728lt5kBiHdE9cZKJHr roVdEbjP0urM3ZBY130 assertion
type: Assertion
description: [Polymorphisms in immunoregulatory genes: towards individualized immunosuppressive therapy?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12083951
was generated by: ECO_0000203

NP56328.RAXPgacyfXOa1O26IUJ4fbo1ItDVmgTm625HDYG223o7A
has assertion: NP56328.RAXPgacyfXOa1O26IUJ4fbo1ItDVmgTm625HDYG223o7A130 assertion
has provenance: NP56328.RAXPgacyfXOa1O26IUJ4fbo1ItDVmgTm625HDYG223o7A130 provenance
has publication info: NP56328.RAXPgacyfXOa1O26IUJ4fbo1ItDVmgTm625HDYG223o7A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56328.RAXPgacyfXOa1O26IUJ4fbo1ItDVmgTm625HDYG223o7A130 assertion
type: Assertion
description: [Association of an interleukin 1B gene polymorphism (-511) with Parkinson's disease in Finnish patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12070246
was generated by: ECO_0000203

NP56334.RAWAnPWOKbUfJTWc8EUCDv0 WBDfydS-0HVWXe4n-SMKM
has assertion: NP56334.RAWAnPWOKbUfJTWc8EUCDv0 WBDfydS-0HVWXe4n-SMKM130 assertion
has provenance: NP56334.RAWAnPWOKbUfJTWc8EUCDv0 WBDfydS-0HVWXe4n-SMKM130 provenance
has publication info: NP56334.RAWAnPWOKbUfJTWc8EUCDv0 WBDfydS-0HVWXe4n-SMKM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56334.RAWAnPWOKbUfJTWc8EUCDv0 WBDfydS-0HVWXe4n-SMKM130 assertion
type: Assertion
description: [Interleukin-1 alpha polymorphism has influence on late-onset sporadic Parkinson's disease in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17458495
was generated by: ECO_0000203

NP56337.RAbZVneWu4Cpg8UBrg xgi64dmujSbA1xrr5Qw6PK4-TI
has assertion: NP56337.RAbZVneWu4Cpg8UBrg xgi64dmujSbA1xrr5Qw6PK4-TI130 assertion
has provenance: NP56337.RAbZVneWu4Cpg8UBrg xgi64dmujSbA1xrr5Qw6PK4-TI130 provenance
has publication info: NP56337.RAbZVneWu4Cpg8UBrg xgi64dmujSbA1xrr5Qw6PK4-TI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56337.RAbZVneWu4Cpg8UBrg xgi64dmujSbA1xrr5Qw6PK4-TI130 assertion
type: Assertion
description: [ Our study showed association with JIA for the IL-4 -1098 T/G polymorphism. It also underlines the genetic contribution of IL-1 polymorphisms to the pathogenesis of JIA, as another polymorphism within the IL-1beta may influence the risk of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15170937
was generated by: ECO_0000203

NP56348.RAUKO88qR50YZAMFmN74fZMVIvENeZlLM gJb2lZB9pAw
has assertion: NP56348.RAUKO88qR50YZAMFmN74fZMVIvENeZlLM gJb2lZB9pAw130 assertion
has provenance: NP56348.RAUKO88qR50YZAMFmN74fZMVIvENeZlLM gJb2lZB9pAw130 provenance
has publication info: NP56348.RAUKO88qR50YZAMFmN74fZMVIvENeZlLM gJb2lZB9pAw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56348.RAUKO88qR50YZAMFmN74fZMVIvENeZlLM gJb2lZB9pAw130 assertion
type: Assertion
description: [Basal cell carcinoma and variants in genes coding for immune response, DNA repair, folate and iron metabolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15914210
was generated by: ECO_0000203

NP56351.RAZCa9p1N7hUhXiXyN228QSTnkFxigEHZxpyspAK0-tLM
has assertion: NP56351.RAZCa9p1N7hUhXiXyN228QSTnkFxigEHZxpyspAK0-tLM130 assertion
has provenance: NP56351.RAZCa9p1N7hUhXiXyN228QSTnkFxigEHZxpyspAK0-tLM130 provenance
has publication info: NP56351.RAZCa9p1N7hUhXiXyN228QSTnkFxigEHZxpyspAK0-tLM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56351.RAZCa9p1N7hUhXiXyN228QSTnkFxigEHZxpyspAK0-tLM130 assertion
type: Assertion
description: [Cerebral ischaemia is a potent stimulus for expression of genes that may influence recovery.We investigated whether functional polymorphisms in the apolipoprotein E (APOE), insulin-like growth factor-1 (IGF-1), tumor necrosis factor-A (TNF-A), interleukin-1A (IL-1A), interleukin-1B (IL-1B), and interleukin-6 (IL-6) genes are related with outcome after aneurysmal SAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15726267
was generated by: ECO_0000203

NP56352.RAZXj1gIQLRPgG goyW7bSWgpk42LW9GWR6Q9ji3BPBwQ
has assertion: NP56352.RAZXj1gIQLRPgG goyW7bSWgpk42LW9GWR6Q9ji3BPBwQ130 assertion
has provenance: NP56352.RAZXj1gIQLRPgG goyW7bSWgpk42LW9GWR6Q9ji3BPBwQ130 provenance
has publication info: NP56352.RAZXj1gIQLRPgG goyW7bSWgpk42LW9GWR6Q9ji3BPBwQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56352.RAZXj1gIQLRPgG goyW7bSWgpk42LW9GWR6Q9ji3BPBwQ130 assertion
type: Assertion
description: [Our results do not support the hypothesis that genetic variation in select polymorphisms of the IL-1 cluster genes is associated with aneurysmal subarachnoid cerebral hemorrhage. However, the IL-1beta gene may modify disease severity and may be regarded as disease severity gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20495422
was generated by: ECO_0000203

NP56357.RATJxi 2flSQWEOxHar3HljHsd3JTq8A8j0vgNv2UHKC4
has assertion: NP56357.RATJxi 2flSQWEOxHar3HljHsd3JTq8A8j0vgNv2UHKC4130 assertion
has provenance: NP56357.RATJxi 2flSQWEOxHar3HljHsd3JTq8A8j0vgNv2UHKC4130 provenance
has publication info: NP56357.RATJxi 2flSQWEOxHar3HljHsd3JTq8A8j0vgNv2UHKC4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56357.RATJxi 2flSQWEOxHar3HljHsd3JTq8A8j0vgNv2UHKC4130 assertion
type: Assertion
description: [However, there are controversial findings from other studies which revealed no significant associations between these polymorphisms and AD; thus further evaluation of the association of IL-1 gene polymorphisms with AD and their role in pathogenesis is needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12525884
was generated by: ECO_0000203

NP56365.RAUzpUHNojPVkA0XMU612LbkwZQDGcC2YrlxG1SiklgB0
has assertion: NP56365.RAUzpUHNojPVkA0XMU612LbkwZQDGcC2YrlxG1SiklgB0130 assertion
has provenance: NP56365.RAUzpUHNojPVkA0XMU612LbkwZQDGcC2YrlxG1SiklgB0130 provenance
has publication info: NP56365.RAUzpUHNojPVkA0XMU612LbkwZQDGcC2YrlxG1SiklgB0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56365.RAUzpUHNojPVkA0XMU612LbkwZQDGcC2YrlxG1SiklgB0130 assertion
type: Assertion
description: [These findings suggest that - with the possible exception of IL-1beta- genetic variation associated with differential expression of the selected pro- and anti-inflammatory cytokines is unlikely to play a major role in susceptibility to and prognosis in CMM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14675394
was generated by: ECO_0000203

NP56367.RAWMyYVoQCM2POUU-ED kDdMfb-hkz-sMtiDN5RGuwqAY
has assertion: NP56367.RAWMyYVoQCM2POUU-ED kDdMfb-hkz-sMtiDN5RGuwqAY130 assertion
has provenance: NP56367.RAWMyYVoQCM2POUU-ED kDdMfb-hkz-sMtiDN5RGuwqAY130 provenance
has publication info: NP56367.RAWMyYVoQCM2POUU-ED kDdMfb-hkz-sMtiDN5RGuwqAY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56367.RAWMyYVoQCM2POUU-ED kDdMfb-hkz-sMtiDN5RGuwqAY130 assertion
type: Assertion
description: [These data suggest that inflammation or an active immune response may induce an increased amount of HTLV-I-infected T cells, leading to a high provirus load.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12651071
was generated by: ECO_0000203

NP56371.RAc9TgH0Opg8Gy-QJ3r39B70ICuQHrpd9D1EDWHzK H-w
has assertion: NP56371.RAc9TgH0Opg8Gy-QJ3r39B70ICuQHrpd9D1EDWHzK H-w130 assertion
has provenance: NP56371.RAc9TgH0Opg8Gy-QJ3r39B70ICuQHrpd9D1EDWHzK H-w130 provenance
has publication info: NP56371.RAc9TgH0Opg8Gy-QJ3r39B70ICuQHrpd9D1EDWHzK H-w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56371.RAc9TgH0Opg8Gy-QJ3r39B70ICuQHrpd9D1EDWHzK H-w130 assertion
type: Assertion
description: [Interleukin-1 (IL-1) and tumor necrosis factor-alpha (TNF-alpha) are potent immunomodulators and proinflammatory cytokines that have been implicated in the pathogenesis of autoimmune and infectious diseases and proposed to be risk factors for LAgP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18587204
was generated by: ECO_0000203

NP56379.RAbH2CzTxub HHg9yYCYEp2T5gY5oRBKlmBCKAcWkM kE
has assertion: NP56379.RAbH2CzTxub HHg9yYCYEp2T5gY5oRBKlmBCKAcWkM kE130 assertion
has provenance: NP56379.RAbH2CzTxub HHg9yYCYEp2T5gY5oRBKlmBCKAcWkM kE130 provenance
has publication info: NP56379.RAbH2CzTxub HHg9yYCYEp2T5gY5oRBKlmBCKAcWkM kE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56379.RAbH2CzTxub HHg9yYCYEp2T5gY5oRBKlmBCKAcWkM kE130 assertion
type: Assertion
description: [To make investigations on the polymorphism of interleukin-1 (IL-1)gene in Chinese Han population, on its association with essential hypertension, and on the relationship between the genotype of IL-1 and susceptibility to essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15476179
was generated by: ECO_0000203

NP56381.RAfxwIAqQ3pdELKE2HBYoktaPjeplhWXbKixjdn7I2GHE
has assertion: NP56381.RAfxwIAqQ3pdELKE2HBYoktaPjeplhWXbKixjdn7I2GHE130 assertion
has provenance: NP56381.RAfxwIAqQ3pdELKE2HBYoktaPjeplhWXbKixjdn7I2GHE130 provenance
has publication info: NP56381.RAfxwIAqQ3pdELKE2HBYoktaPjeplhWXbKixjdn7I2GHE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56381.RAfxwIAqQ3pdELKE2HBYoktaPjeplhWXbKixjdn7I2GHE130 assertion
type: Assertion
description: [The IL-6 G-174C polymorphism may be associated with ischaemic stroke in patients without a history of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16323614
was generated by: ECO_0000203

NP56384.RAXco9C-y2evOn4YiCfVSxvKIp p-EcaKpiWCvSH0gTCs
has assertion: NP56384.RAXco9C-y2evOn4YiCfVSxvKIp p-EcaKpiWCvSH0gTCs130 assertion
has provenance: NP56384.RAXco9C-y2evOn4YiCfVSxvKIp p-EcaKpiWCvSH0gTCs130 provenance
has publication info: NP56384.RAXco9C-y2evOn4YiCfVSxvKIp p-EcaKpiWCvSH0gTCs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56384.RAXco9C-y2evOn4YiCfVSxvKIp p-EcaKpiWCvSH0gTCs130 assertion
type: Assertion
description: [We examined the association between malignant lymphoma risk and the polymorphisms of the IL-1 gene family IL-1B -31 C/T, IL-1A -889 C/T, and IL-1RN 86-bp variable number of terminal repeat (VNTR) and myeloperoxidase (MPO -463 G/A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11423389
was generated by: ECO_0000203

NP56390.RAVKUGlrCl801d0DyRWWkR4VC1yWP3wwcSXn Ub7R CGY
has assertion: NP56390.RAVKUGlrCl801d0DyRWWkR4VC1yWP3wwcSXn Ub7R CGY130 assertion
has provenance: NP56390.RAVKUGlrCl801d0DyRWWkR4VC1yWP3wwcSXn Ub7R CGY130 provenance
has publication info: NP56390.RAVKUGlrCl801d0DyRWWkR4VC1yWP3wwcSXn Ub7R CGY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56390.RAVKUGlrCl801d0DyRWWkR4VC1yWP3wwcSXn Ub7R CGY130 assertion
type: Assertion
description: [The present study suggests that genetic factors are associated with susceptibility to develop symptomatic dental abscesses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17511783
was generated by: ECO_0000203

NP56398.RAaNfSOAx-3mPF6iYNFnV0NV 90oTzgtVlUS9g6eOmW6Y
has assertion: NP56398.RAaNfSOAx-3mPF6iYNFnV0NV 90oTzgtVlUS9g6eOmW6Y130 assertion
has provenance: NP56398.RAaNfSOAx-3mPF6iYNFnV0NV 90oTzgtVlUS9g6eOmW6Y130 provenance
has publication info: NP56398.RAaNfSOAx-3mPF6iYNFnV0NV 90oTzgtVlUS9g6eOmW6Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56398.RAaNfSOAx-3mPF6iYNFnV0NV 90oTzgtVlUS9g6eOmW6Y130 assertion
type: Assertion
description: [Association analysis of IL1A and IL1B variants in alopecia areata.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11703512
was generated by: ECO_0000203

NP56412.RAYhfJ2QXaRqAHRI1DD7apCIzRujCXS5ZyB7BLmgPdtfE
has assertion: NP56412.RAYhfJ2QXaRqAHRI1DD7apCIzRujCXS5ZyB7BLmgPdtfE130 assertion
has provenance: NP56412.RAYhfJ2QXaRqAHRI1DD7apCIzRujCXS5ZyB7BLmgPdtfE130 provenance
has publication info: NP56412.RAYhfJ2QXaRqAHRI1DD7apCIzRujCXS5ZyB7BLmgPdtfE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56412.RAYhfJ2QXaRqAHRI1DD7apCIzRujCXS5ZyB7BLmgPdtfE130 assertion
type: Assertion
description: [A comprehensive analysis of 207 SNP of 11 cytokine genes revealed that variations in IL-4 and IL-1RN genes are negatively associated with the risk of developing gastric cancer following H. pylori infection. Distinct host cytokine responses in the gastric mucosa might have a role in H. pylori-induced carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17444864
was generated by: ECO_0000203

NP56414.RATeu1 bbKLFNtO3BoUoDEpRdwwdV0e3Cbsv24choW25U
has assertion: NP56414.RATeu1 bbKLFNtO3BoUoDEpRdwwdV0e3Cbsv24choW25U130 assertion
has provenance: NP56414.RATeu1 bbKLFNtO3BoUoDEpRdwwdV0e3Cbsv24choW25U130 provenance
has publication info: NP56414.RATeu1 bbKLFNtO3BoUoDEpRdwwdV0e3Cbsv24choW25U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56414.RATeu1 bbKLFNtO3BoUoDEpRdwwdV0e3Cbsv24choW25U130 assertion
type: Assertion
description: [Our data do not provide evidence for an association between the polymorphic variants of the IL-1B and COMT genes and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17385677
was generated by: ECO_0000203

NP56415.RARLn8UCvTJbIcZo2TcBuWdWKuMGNl-yhW7j-ET aClHo
has assertion: NP56415.RARLn8UCvTJbIcZo2TcBuWdWKuMGNl-yhW7j-ET aClHo130 assertion
has provenance: NP56415.RARLn8UCvTJbIcZo2TcBuWdWKuMGNl-yhW7j-ET aClHo130 provenance
has publication info: NP56415.RARLn8UCvTJbIcZo2TcBuWdWKuMGNl-yhW7j-ET aClHo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56415.RARLn8UCvTJbIcZo2TcBuWdWKuMGNl-yhW7j-ET aClHo130 assertion
type: Assertion
description: [In the present case-control study, we ascertained three polymorphisms of the IL1 gene cluster -889 C/T polymorphism of the IL1alpha gene (IL1A), -511 C/T polymorphism of the IL1beta promoter (IL1B promoter), a polymorphism of IL1beta exon 5 (IL1B exon 5), an 86-bp repeat in intron 2 of the IL1 receptor antagonist gene (IL1RN), and the -174 G/C polymorphism of the IL6 gene (IL6) in 269 patients with breast cancer and 227 healthy controls using PCR and pyrosequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16115908
was generated by: ECO_0000203

NP56418.RAX4roAvYpYd6XDGKnkCynTVaJ1DtTvmVDdqVlDWuFTjc
has assertion: NP56418.RAX4roAvYpYd6XDGKnkCynTVaJ1DtTvmVDdqVlDWuFTjc130 assertion
has provenance: NP56418.RAX4roAvYpYd6XDGKnkCynTVaJ1DtTvmVDdqVlDWuFTjc130 provenance
has publication info: NP56418.RAX4roAvYpYd6XDGKnkCynTVaJ1DtTvmVDdqVlDWuFTjc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56418.RAX4roAvYpYd6XDGKnkCynTVaJ1DtTvmVDdqVlDWuFTjc130 assertion
type: Assertion
description: [Polymorphisms in cytokine genes and serum cytokine levels among New Mexican women with and without breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20418110
was generated by: ECO_0000203

NP56420.RAVQXNz26VAzKZtb-DSooY96WMx6tCtbhhPKb3GxilbQ0
has assertion: NP56420.RAVQXNz26VAzKZtb-DSooY96WMx6tCtbhhPKb3GxilbQ0130 assertion
has provenance: NP56420.RAVQXNz26VAzKZtb-DSooY96WMx6tCtbhhPKb3GxilbQ0130 provenance
has publication info: NP56420.RAVQXNz26VAzKZtb-DSooY96WMx6tCtbhhPKb3GxilbQ0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56420.RAVQXNz26VAzKZtb-DSooY96WMx6tCtbhhPKb3GxilbQ0130 assertion
type: Assertion
description: [TNF2 plays an important role in the susceptibility of cachexia in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18953879
was generated by: ECO_0000203

NP56429.RAU72fzz-7LWzofhfm6F9sF579zudE 49I-6svDfBUBVs
has assertion: NP56429.RAU72fzz-7LWzofhfm6F9sF579zudE 49I-6svDfBUBVs130 assertion
has provenance: NP56429.RAU72fzz-7LWzofhfm6F9sF579zudE 49I-6svDfBUBVs130 provenance
has publication info: NP56429.RAU72fzz-7LWzofhfm6F9sF579zudE 49I-6svDfBUBVs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56429.RAU72fzz-7LWzofhfm6F9sF579zudE 49I-6svDfBUBVs130 assertion
type: Assertion
description: [ Genetic variations in cytokine and DNA repair genes contribute to susceptibility to HBV-related HCC. Smoking increased such genetic susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16172101
was generated by: ECO_0000203

NP56437.RAa4iLD6Ubt9xJJASjt3WWpXtHtZW8S6fpqfreubjhcoY
has assertion: NP56437.RAa4iLD6Ubt9xJJASjt3WWpXtHtZW8S6fpqfreubjhcoY130 assertion
has provenance: NP56437.RAa4iLD6Ubt9xJJASjt3WWpXtHtZW8S6fpqfreubjhcoY130 provenance
has publication info: NP56437.RAa4iLD6Ubt9xJJASjt3WWpXtHtZW8S6fpqfreubjhcoY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56437.RAa4iLD6Ubt9xJJASjt3WWpXtHtZW8S6fpqfreubjhcoY130 assertion
type: Assertion
description: [ None of the markers tested were shown to be associated with increased or decreased risk of RA. The rarer alleles of IL-4 VNTR and IL-1B (-511) appear to be associated with a less severe course in RA of long duration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12115161
was generated by: ECO_0000203

NP56439.RAS-s-LduRLdR5OAZJ0lPrHVgs95EiVuyARuAJrIFXC-s
has assertion: NP56439.RAS-s-LduRLdR5OAZJ0lPrHVgs95EiVuyARuAJrIFXC-s130 assertion
has provenance: NP56439.RAS-s-LduRLdR5OAZJ0lPrHVgs95EiVuyARuAJrIFXC-s130 provenance
has publication info: NP56439.RAS-s-LduRLdR5OAZJ0lPrHVgs95EiVuyARuAJrIFXC-s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56439.RAS-s-LduRLdR5OAZJ0lPrHVgs95EiVuyARuAJrIFXC-s130 assertion
type: Assertion
description: [The purpose of this study was to evaluate whether IL-1 beta (IL-1beta promoter and IL-1beta exon 5), IL-1 receptor antagonist (IL-1 Ra), and IL-4 (IL-4 promoter and IL-4 intron 3) gene polymorphisms act as markers of susceptibility to Kawasaki disease (KD), or of the severity of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15900570
was generated by: ECO_0000203

NP56442.RAUV01QEjV-bI2CHZiK4WgUZ7wY8DsESFz92zTzb3mWe8
has assertion: NP56442.RAUV01QEjV-bI2CHZiK4WgUZ7wY8DsESFz92zTzb3mWe8130 assertion
has provenance: NP56442.RAUV01QEjV-bI2CHZiK4WgUZ7wY8DsESFz92zTzb3mWe8130 provenance
has publication info: NP56442.RAUV01QEjV-bI2CHZiK4WgUZ7wY8DsESFz92zTzb3mWe8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56442.RAUV01QEjV-bI2CHZiK4WgUZ7wY8DsESFz92zTzb3mWe8130 assertion
type: Assertion
description: [ Our results suggest that the -511 CC genotype of the IL1B gene could be related to resistance to bisphosphonates in patients with PDB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16257277
was generated by: ECO_0000203

NP56447.RAeWQTBbQUva86-RbSgwbp2F3BPx-9H64mokJLp1rbRHA
has assertion: NP56447.RAeWQTBbQUva86-RbSgwbp2F3BPx-9H64mokJLp1rbRHA130 assertion
has provenance: NP56447.RAeWQTBbQUva86-RbSgwbp2F3BPx-9H64mokJLp1rbRHA130 provenance
has publication info: NP56447.RAeWQTBbQUva86-RbSgwbp2F3BPx-9H64mokJLp1rbRHA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56447.RAeWQTBbQUva86-RbSgwbp2F3BPx-9H64mokJLp1rbRHA130 assertion
type: Assertion
description: [No association was found in either allele frequency or genotype distribution of IL1RN and IL1B polymorphisms between CAD and the control groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19142372
was generated by: ECO_0000203

NP56459.RAaCBVCAzajYpzir1mYNAIH91eA7UVR4F9XPGw8LcxC9k
has assertion: NP56459.RAaCBVCAzajYpzir1mYNAIH91eA7UVR4F9XPGw8LcxC9k130 assertion
has provenance: NP56459.RAaCBVCAzajYpzir1mYNAIH91eA7UVR4F9XPGw8LcxC9k130 provenance
has publication info: NP56459.RAaCBVCAzajYpzir1mYNAIH91eA7UVR4F9XPGw8LcxC9k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56459.RAaCBVCAzajYpzir1mYNAIH91eA7UVR4F9XPGw8LcxC9k130 assertion
type: Assertion
description: [T helper 1-type immunity to trophoblast antigens in women with a history of recurrent pregnancy loss is associated with polymorphism of the IL1B promoter region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11857060
was generated by: ECO_0000203

NP56465.RAReaPTLQSl64sM0Nh vuYQKg7g-63wQX3yXehR0wGb k
has assertion: NP56465.RAReaPTLQSl64sM0Nh vuYQKg7g-63wQX3yXehR0wGb k130 assertion
has provenance: NP56465.RAReaPTLQSl64sM0Nh vuYQKg7g-63wQX3yXehR0wGb k130 provenance
has publication info: NP56465.RAReaPTLQSl64sM0Nh vuYQKg7g-63wQX3yXehR0wGb k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56465.RAReaPTLQSl64sM0Nh vuYQKg7g-63wQX3yXehR0wGb k130 assertion
type: Assertion
description: [Analysis of multiple candidate genes in association with phenotypes of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20378664
was generated by: ECO_0000203

NP56468.RAS6abPB4Z0hdk-Gz5JCBzW9XUnOiO1oGPcBKc ikHbTw
has assertion: NP56468.RAS6abPB4Z0hdk-Gz5JCBzW9XUnOiO1oGPcBKc ikHbTw130 assertion
has provenance: NP56468.RAS6abPB4Z0hdk-Gz5JCBzW9XUnOiO1oGPcBKc ikHbTw130 provenance
has publication info: NP56468.RAS6abPB4Z0hdk-Gz5JCBzW9XUnOiO1oGPcBKc ikHbTw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56468.RAS6abPB4Z0hdk-Gz5JCBzW9XUnOiO1oGPcBKc ikHbTw130 assertion
type: Assertion
description: [The interleukin-1 gene family in multiple sclerosis susceptibility and disease course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14664464
was generated by: ECO_0000203

NP56473.RAYx94ER168lCHKetgWgyGNuOliExLVcftKkv1wky2VAU
has assertion: NP56473.RAYx94ER168lCHKetgWgyGNuOliExLVcftKkv1wky2VAU130 assertion
has provenance: NP56473.RAYx94ER168lCHKetgWgyGNuOliExLVcftKkv1wky2VAU130 provenance
has publication info: NP56473.RAYx94ER168lCHKetgWgyGNuOliExLVcftKkv1wky2VAU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56473.RAYx94ER168lCHKetgWgyGNuOliExLVcftKkv1wky2VAU130 assertion
type: Assertion
description: [Association studies of 33 single nucleotide polymorphisms (SNPs) in 29 candidate genes for bronchial asthma: positive association a T924C polymorphism in the thromboxane A2 receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10830912
was generated by: ECO_0000203

NP56476.RAaxw8LGSnDS4m wQE4eCxtulpo6gS9HAhgVO-lnsRF-g
has assertion: NP56476.RAaxw8LGSnDS4m wQE4eCxtulpo6gS9HAhgVO-lnsRF-g130 assertion
has provenance: NP56476.RAaxw8LGSnDS4m wQE4eCxtulpo6gS9HAhgVO-lnsRF-g130 provenance
has publication info: NP56476.RAaxw8LGSnDS4m wQE4eCxtulpo6gS9HAhgVO-lnsRF-g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56476.RAaxw8LGSnDS4m wQE4eCxtulpo6gS9HAhgVO-lnsRF-g130 assertion
type: Assertion
description: [ None of the markers tested were shown to be associated with increased or decreased risk of RA. The rarer alleles of IL-4 VNTR and IL-1B (-511) appear to be associated with a less severe course in RA of long duration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12115161
was generated by: ECO_0000203

NP56482.RAcy6TRhUGY79F84rRZyHJ2j0uZekuOfaxHtSxsgA7z2Y
has assertion: NP56482.RAcy6TRhUGY79F84rRZyHJ2j0uZekuOfaxHtSxsgA7z2Y130 assertion
has provenance: NP56482.RAcy6TRhUGY79F84rRZyHJ2j0uZekuOfaxHtSxsgA7z2Y130 provenance
has publication info: NP56482.RAcy6TRhUGY79F84rRZyHJ2j0uZekuOfaxHtSxsgA7z2Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56482.RAcy6TRhUGY79F84rRZyHJ2j0uZekuOfaxHtSxsgA7z2Y130 assertion
type: Assertion
description: [Overexpression of the pluripotent cytokine interleukin-1 (IL-1) by microglial cells correlates with formation of neuritic beta-amyloid plaques in Alzheimer's disease (AD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10716256
was generated by: ECO_0000203

NP56483.RAaKnjTXUHemVceSh6EIDZT lu0lzbtz5S3exozw 7Lkc
has assertion: NP56483.RAaKnjTXUHemVceSh6EIDZT lu0lzbtz5S3exozw 7Lkc130 assertion
has provenance: NP56483.RAaKnjTXUHemVceSh6EIDZT lu0lzbtz5S3exozw 7Lkc130 provenance
has publication info: NP56483.RAaKnjTXUHemVceSh6EIDZT lu0lzbtz5S3exozw 7Lkc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56483.RAaKnjTXUHemVceSh6EIDZT lu0lzbtz5S3exozw 7Lkc130 assertion
type: Assertion
description: [Extensive, previous evidence (reviewed here) indicates an important role for noradrenaline in the control of inflammation in the brain. Thus, the -1021T allele with presumed low activity may be associated with misregulation of inflammation, which could contribute to the onset of AD. We suggest that such misregulation is the predominant mechanism of the association we report here.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21070631
was generated by: ECO_0000203

NP56484.RAU7-h8zv62xCrvz4-BsunT-5nspb94RkgDakkhPJJpMs
has assertion: NP56484.RAU7-h8zv62xCrvz4-BsunT-5nspb94RkgDakkhPJJpMs130 assertion
has provenance: NP56484.RAU7-h8zv62xCrvz4-BsunT-5nspb94RkgDakkhPJJpMs130 provenance
has publication info: NP56484.RAU7-h8zv62xCrvz4-BsunT-5nspb94RkgDakkhPJJpMs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56484.RAU7-h8zv62xCrvz4-BsunT-5nspb94RkgDakkhPJJpMs130 assertion
type: Assertion
description: [The findings support the association of several loci with AD, and suggest how intermediate phenotypes can enhance analysis of susceptibility loci in this complex genetic disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20574532
was generated by: ECO_0000203

NP56486.RATule18wdXmt1 seMxcCZw4mfMsBAuXyHfGIDMkxvF2s
has assertion: NP56486.RATule18wdXmt1 seMxcCZw4mfMsBAuXyHfGIDMkxvF2s130 assertion
has provenance: NP56486.RATule18wdXmt1 seMxcCZw4mfMsBAuXyHfGIDMkxvF2s130 provenance
has publication info: NP56486.RATule18wdXmt1 seMxcCZw4mfMsBAuXyHfGIDMkxvF2s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56486.RATule18wdXmt1 seMxcCZw4mfMsBAuXyHfGIDMkxvF2s130 assertion
type: Assertion
description: [Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20413850
was generated by: ECO_0000203

NP56491.RAREIUxlx5KjmnUE6FwuRkKjt088aqd3cyGgNJmmzXGTM
has assertion: NP56491.RAREIUxlx5KjmnUE6FwuRkKjt088aqd3cyGgNJmmzXGTM130 assertion
has provenance: NP56491.RAREIUxlx5KjmnUE6FwuRkKjt088aqd3cyGgNJmmzXGTM130 provenance
has publication info: NP56491.RAREIUxlx5KjmnUE6FwuRkKjt088aqd3cyGgNJmmzXGTM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56491.RAREIUxlx5KjmnUE6FwuRkKjt088aqd3cyGgNJmmzXGTM130 assertion
type: Assertion
description: [ Our study showed association with JIA for the IL-4 -1098 T/G polymorphism. It also underlines the genetic contribution of IL-1 polymorphisms to the pathogenesis of JIA, as another polymorphism within the IL-1beta may influence the risk of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15170937
was generated by: ECO_0000203

NP56498.RAcdihNgF-QXivIUNj1nHsDNblAFaO6VgzgiVIeF5WMpY
has assertion: NP56498.RAcdihNgF-QXivIUNj1nHsDNblAFaO6VgzgiVIeF5WMpY130 assertion
has provenance: NP56498.RAcdihNgF-QXivIUNj1nHsDNblAFaO6VgzgiVIeF5WMpY130 provenance
has publication info: NP56498.RAcdihNgF-QXivIUNj1nHsDNblAFaO6VgzgiVIeF5WMpY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56498.RAcdihNgF-QXivIUNj1nHsDNblAFaO6VgzgiVIeF5WMpY130 assertion
type: Assertion
description: [Genetic polymorphisms of IL-1A, IL-1B, IL-1RN, NFKB1, FAS, and FASL, and risk of silicosis in a Chinese occupational population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18666137
was generated by: ECO_0000203

NP56499.RAXox110fjMiyCzQA3o6OIu55OxCgws1b5ZESQ7VqDGac
has assertion: NP56499.RAXox110fjMiyCzQA3o6OIu55OxCgws1b5ZESQ7VqDGac130 assertion
has provenance: NP56499.RAXox110fjMiyCzQA3o6OIu55OxCgws1b5ZESQ7VqDGac130 provenance
has publication info: NP56499.RAXox110fjMiyCzQA3o6OIu55OxCgws1b5ZESQ7VqDGac130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56499.RAXox110fjMiyCzQA3o6OIu55OxCgws1b5ZESQ7VqDGac130 assertion
type: Assertion
description: [Cerebral ischaemia is a potent stimulus for expression of genes that may influence recovery.We investigated whether functional polymorphisms in the apolipoprotein E (APOE), insulin-like growth factor-1 (IGF-1), tumor necrosis factor-A (TNF-A), interleukin-1A (IL-1A), interleukin-1B (IL-1B), and interleukin-6 (IL-6) genes are related with outcome after aneurysmal SAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15726267
was generated by: ECO_0000203

NP56501.RASa4WPYG62CLJoa9mupxiXPZQVRY69s5obupa0skT5XE
has assertion: NP56501.RASa4WPYG62CLJoa9mupxiXPZQVRY69s5obupa0skT5XE130 assertion
has provenance: NP56501.RASa4WPYG62CLJoa9mupxiXPZQVRY69s5obupa0skT5XE130 provenance
has publication info: NP56501.RASa4WPYG62CLJoa9mupxiXPZQVRY69s5obupa0skT5XE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56501.RASa4WPYG62CLJoa9mupxiXPZQVRY69s5obupa0skT5XE130 assertion
type: Assertion
description: [Associations with IL6 -174 variants suggest that the C/C genotype has a protective effect (OR=0.13) while carriers of the G allele are more susceptible (OR=7.66) to EPF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15566952
was generated by: ECO_0000203

NP56510.RAdZ7fMU4e8B67IVybRx2QXIPzAsDaPN9AXQ2TI6gW2fc
has assertion: NP56510.RAdZ7fMU4e8B67IVybRx2QXIPzAsDaPN9AXQ2TI6gW2fc130 assertion
has provenance: NP56510.RAdZ7fMU4e8B67IVybRx2QXIPzAsDaPN9AXQ2TI6gW2fc130 provenance
has publication info: NP56510.RAdZ7fMU4e8B67IVybRx2QXIPzAsDaPN9AXQ2TI6gW2fc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56510.RAdZ7fMU4e8B67IVybRx2QXIPzAsDaPN9AXQ2TI6gW2fc130 assertion
type: Assertion
description: [The results show statistically significant (p <or= 0.05) differences between genotype frequencies in aggressive and controls (IL-1B +3954 & IL-6 -174); chronic and controls (IL-6 -174 & VDR -1056); chronic and aggressive periodontitis (IL-1A -889); and periodontitis as a whole and controls (VDR -1056, TLR-4 399 & IL-6 -174).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16304445
was generated by: ECO_0000203

NP56511.RAUKoOiKhOY fn4IFx0nU0KDG-p9u7sw2KpONy79PHXpM
has assertion: NP56511.RAUKoOiKhOY fn4IFx0nU0KDG-p9u7sw2KpONy79PHXpM130 assertion
has provenance: NP56511.RAUKoOiKhOY fn4IFx0nU0KDG-p9u7sw2KpONy79PHXpM130 provenance
has publication info: NP56511.RAUKoOiKhOY fn4IFx0nU0KDG-p9u7sw2KpONy79PHXpM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56511.RAUKoOiKhOY fn4IFx0nU0KDG-p9u7sw2KpONy79PHXpM130 assertion
type: Assertion
description: [To study whether interleukin-1 (IL-1) genotypes and/or alleles were associated with aggressive periodontitis (AgP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16155691
was generated by: ECO_0000203

NP56512.RAUrEGTtcR9tBtR7DqbLjbb8xIZf6K8LZbyV3d-gq9Axk
has assertion: NP56512.RAUrEGTtcR9tBtR7DqbLjbb8xIZf6K8LZbyV3d-gq9Axk130 assertion
has provenance: NP56512.RAUrEGTtcR9tBtR7DqbLjbb8xIZf6K8LZbyV3d-gq9Axk130 provenance
has publication info: NP56512.RAUrEGTtcR9tBtR7DqbLjbb8xIZf6K8LZbyV3d-gq9Axk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56512.RAUrEGTtcR9tBtR7DqbLjbb8xIZf6K8LZbyV3d-gq9Axk130 assertion
type: Assertion
description: [A group of 20 subjects aged more than 35 with clinical and radiographic signs of severe periodontitis (cases) underwent the salivary genetic test to single out the alleles of the genes IL-1A and IL-1B, by the PCR technique.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12874528
was generated by: ECO_0000203

NP56513.RAV7qLji3MmD97fvtSJBOVOnLWXiSS7SaLhzfSKohVzvs
has assertion: NP56513.RAV7qLji3MmD97fvtSJBOVOnLWXiSS7SaLhzfSKohVzvs130 assertion
has provenance: NP56513.RAV7qLji3MmD97fvtSJBOVOnLWXiSS7SaLhzfSKohVzvs130 provenance
has publication info: NP56513.RAV7qLji3MmD97fvtSJBOVOnLWXiSS7SaLhzfSKohVzvs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56513.RAV7qLji3MmD97fvtSJBOVOnLWXiSS7SaLhzfSKohVzvs130 assertion
type: Assertion
description: [(1) There were no significant differences in the distribution of IL-1A-889 among severe CP patients, moderate CP patients, mild CP patients and healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12362317
was generated by: ECO_0000203

NP56516.RAU8vaJtUBCcbDsS5uwU0dvqyPdb-TN2NkfVpo9NCJPDo
has assertion: NP56516.RAU8vaJtUBCcbDsS5uwU0dvqyPdb-TN2NkfVpo9NCJPDo130 assertion
has provenance: NP56516.RAU8vaJtUBCcbDsS5uwU0dvqyPdb-TN2NkfVpo9NCJPDo130 provenance
has publication info: NP56516.RAU8vaJtUBCcbDsS5uwU0dvqyPdb-TN2NkfVpo9NCJPDo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56516.RAU8vaJtUBCcbDsS5uwU0dvqyPdb-TN2NkfVpo9NCJPDo130 assertion
type: Assertion
description: [ Our results suggest that common genetic variants in proinflammatory cytokine genes could influence the risk for spontaneous preterm birth. Selected TNF/LTA haplotypes were associated with spontaneous preterm birth in both African-American and white subjects. Our data do not support an inflammatory etiology for SGA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15951664
was generated by: ECO_0000203

NP56518.RAVwTAPMlTvNPytmfGdIStwtXqE87DPGDfAD8D KzRhrA
has assertion: NP56518.RAVwTAPMlTvNPytmfGdIStwtXqE87DPGDfAD8D KzRhrA130 assertion
has provenance: NP56518.RAVwTAPMlTvNPytmfGdIStwtXqE87DPGDfAD8D KzRhrA130 provenance
has publication info: NP56518.RAVwTAPMlTvNPytmfGdIStwtXqE87DPGDfAD8D KzRhrA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56518.RAVwTAPMlTvNPytmfGdIStwtXqE87DPGDfAD8D KzRhrA130 assertion
type: Assertion
description: [These studies identify single locus associations with preterm birth for both maternal and fetal genotypes in two populations of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20140262
was generated by: ECO_0000203

NP56527.RAWwbWNP-pD2R RpcAFzGRDS0FQCd93DaDw3-BgTfduSE
has assertion: NP56527.RAWwbWNP-pD2R RpcAFzGRDS0FQCd93DaDw3-BgTfduSE130 assertion
has provenance: NP56527.RAWwbWNP-pD2R RpcAFzGRDS0FQCd93DaDw3-BgTfduSE130 provenance
has publication info: NP56527.RAWwbWNP-pD2R RpcAFzGRDS0FQCd93DaDw3-BgTfduSE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56527.RAWwbWNP-pD2R RpcAFzGRDS0FQCd93DaDw3-BgTfduSE130 assertion
type: Assertion
description: [ Allele IL-1RN2 polymorphism, but not IL-1A or IL-1B gene polymorphism, is associated with susceptibility to sepsis. Alleles A2, B2 and RN2 might be important high-risk genetic markers for sepsis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12425801
was generated by: ECO_0000203

NP56528.RAYnQPq0EiSsyTip55QCR16CQ0dcN 5YRXAvvTrVYj-ik
has assertion: NP56528.RAYnQPq0EiSsyTip55QCR16CQ0dcN 5YRXAvvTrVYj-ik130 assertion
has provenance: NP56528.RAYnQPq0EiSsyTip55QCR16CQ0dcN 5YRXAvvTrVYj-ik130 provenance
has publication info: NP56528.RAYnQPq0EiSsyTip55QCR16CQ0dcN 5YRXAvvTrVYj-ik130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56528.RAYnQPq0EiSsyTip55QCR16CQ0dcN 5YRXAvvTrVYj-ik130 assertion
type: Assertion
description: [Our analysis of these SNP in the IL-1 complex and NF-kappaB genes does not support a major role for either in AS susceptibility in the Seoul and Toronto populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16206345
was generated by: ECO_0000203

NP56532.RAfDUV2OXkFzL9mLT7T2rtlplCccPoV83JoO5wapami88
has assertion: NP56532.RAfDUV2OXkFzL9mLT7T2rtlplCccPoV83JoO5wapami88130 assertion
has provenance: NP56532.RAfDUV2OXkFzL9mLT7T2rtlplCccPoV83JoO5wapami88130 provenance
has publication info: NP56532.RAfDUV2OXkFzL9mLT7T2rtlplCccPoV83JoO5wapami88130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56532.RAfDUV2OXkFzL9mLT7T2rtlplCccPoV83JoO5wapami88130 assertion
type: Assertion
description: [In conclusion, no association of the IL1B C(minus sign?31)T with HT was found, whereas combined frequency of the minor alleles of the IL1RN polymorphism was increased in the HT cohort studied]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11840488
was generated by: ECO_0000203

NP56534.RAUWFPn bZRNlEv HkstFjW7kGolR 4ABgtG3BXPVGJAQ
has assertion: NP56534.RAUWFPn bZRNlEv HkstFjW7kGolR 4ABgtG3BXPVGJAQ130 assertion
has provenance: NP56534.RAUWFPn bZRNlEv HkstFjW7kGolR 4ABgtG3BXPVGJAQ130 provenance
has publication info: NP56534.RAUWFPn bZRNlEv HkstFjW7kGolR 4ABgtG3BXPVGJAQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56534.RAUWFPn bZRNlEv HkstFjW7kGolR 4ABgtG3BXPVGJAQ130 assertion
type: Assertion
description: [These results suggest that these polymorphisms might confer a greater susceptibility to develop dysthymia in Brazilian patients. However, to validate these data it will be of great interest to repeat this study in larger samples and other ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14997019
was generated by: ECO_0000203

NP56537.RATBHMLhvnL0fdIpm65XOTKS5CwmWEnZDcpaUiHLnayIM
has assertion: NP56537.RATBHMLhvnL0fdIpm65XOTKS5CwmWEnZDcpaUiHLnayIM130 assertion
has provenance: NP56537.RATBHMLhvnL0fdIpm65XOTKS5CwmWEnZDcpaUiHLnayIM130 provenance
has publication info: NP56537.RATBHMLhvnL0fdIpm65XOTKS5CwmWEnZDcpaUiHLnayIM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56537.RATBHMLhvnL0fdIpm65XOTKS5CwmWEnZDcpaUiHLnayIM130 assertion
type: Assertion
description: [ The IL-1alpha-889 polymorphism, previously shown to predispose to increased IL-1 protein expression, may be involved in susceptibility to SSc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14705223
was generated by: ECO_0000203

NP56538.RAVclFJyvno-w3gWASSmpFIyDeR9p7S2iumdssSHdB298
has assertion: NP56538.RAVclFJyvno-w3gWASSmpFIyDeR9p7S2iumdssSHdB298130 assertion
has provenance: NP56538.RAVclFJyvno-w3gWASSmpFIyDeR9p7S2iumdssSHdB298130 provenance
has publication info: NP56538.RAVclFJyvno-w3gWASSmpFIyDeR9p7S2iumdssSHdB298130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56538.RAVclFJyvno-w3gWASSmpFIyDeR9p7S2iumdssSHdB298130 assertion
type: Assertion
description: [To analyze the frequencies of haplotypes of single-nucleotide polymorphisms (SNPs) of the IL1A gene (at -889, +4729, and +4845) in patients with systemic sclerosis (SSc) and in healthy control subjects, and to determine whether the IL1A gene haplotype is associated with SSc susceptibility or disease severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12528118
was generated by: ECO_0000203

NP56539.RAQuT3w-HmEikntzM -fJNwYr3ozKm96zsFEfS3Hifybs
has assertion: NP56539.RAQuT3w-HmEikntzM -fJNwYr3ozKm96zsFEfS3Hifybs130 assertion
has provenance: NP56539.RAQuT3w-HmEikntzM -fJNwYr3ozKm96zsFEfS3Hifybs130 provenance
has publication info: NP56539.RAQuT3w-HmEikntzM -fJNwYr3ozKm96zsFEfS3Hifybs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56539.RAQuT3w-HmEikntzM -fJNwYr3ozKm96zsFEfS3Hifybs130 assertion
type: Assertion
description: [Interleukin (IL)1alpha and IL1beta, and their endogenous receptor antagonist (IL1Ra), have been related to the pathology of systemic lupus erythematosus (SLE), but the role of IL1 polymorphisms in the aetiology of SLE is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14672899
was generated by: ECO_0000203

NP56540.RAfBEQUHPSPL-lWSJ36dr8PDm7THr3WEpBnFR3U-L2t A
has assertion: NP56540.RAfBEQUHPSPL-lWSJ36dr8PDm7THr3WEpBnFR3U-L2t A130 assertion
has provenance: NP56540.RAfBEQUHPSPL-lWSJ36dr8PDm7THr3WEpBnFR3U-L2t A130 provenance
has publication info: NP56540.RAfBEQUHPSPL-lWSJ36dr8PDm7THr3WEpBnFR3U-L2t A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56540.RAfBEQUHPSPL-lWSJ36dr8PDm7THr3WEpBnFR3U-L2t A130 assertion
type: Assertion
description: [ Our findings suggest that the IL-1 gene cluster polymorphisms may play a significant role in the pathogenesis of OA of the hip.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15077300
was generated by: ECO_0000203

NP56542.RATu5RDBRh9hVtjMlKcWmf5LNWqVxmuwYhbh8 AxoSK3I
has assertion: NP56542.RATu5RDBRh9hVtjMlKcWmf5LNWqVxmuwYhbh8 AxoSK3I130 assertion
has provenance: NP56542.RATu5RDBRh9hVtjMlKcWmf5LNWqVxmuwYhbh8 AxoSK3I130 provenance
has publication info: NP56542.RATu5RDBRh9hVtjMlKcWmf5LNWqVxmuwYhbh8 AxoSK3I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56542.RATu5RDBRh9hVtjMlKcWmf5LNWqVxmuwYhbh8 AxoSK3I130 assertion
type: Assertion
description: [Interleukin-1 region meta-analysis with osteoarthritis phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19733643
was generated by: ECO_0000203

NP56543.RAXdOh9PUBRbr3 xzKd-oZLRh aB DA3 V01krFG7HIE
has assertion: NP56543.RAXdOh9PUBRbr3 xzKd-oZLRh aB DA3 V01krFG7HIE130 assertion
has provenance: NP56543.RAXdOh9PUBRbr3 xzKd-oZLRh aB DA3 V01krFG7HIE130 provenance
has publication info: NP56543.RAXdOh9PUBRbr3 xzKd-oZLRh aB DA3 V01krFG7HIE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56543.RAXdOh9PUBRbr3 xzKd-oZLRh aB DA3 V01krFG7HIE130 assertion
type: Assertion
description: [Association of interleukin-1 alpha gene polymorphism with cerebral infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12824054
was generated by: ECO_0000203

NP56546.RAU8Mtma5zHlfbQwwlGdotHN6QBDuc8W5Ilh8o-mNPgOY
has assertion: NP56546.RAU8Mtma5zHlfbQwwlGdotHN6QBDuc8W5Ilh8o-mNPgOY130 assertion
has provenance: NP56546.RAU8Mtma5zHlfbQwwlGdotHN6QBDuc8W5Ilh8o-mNPgOY130 provenance
has publication info: NP56546.RAU8Mtma5zHlfbQwwlGdotHN6QBDuc8W5Ilh8o-mNPgOY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56546.RAU8Mtma5zHlfbQwwlGdotHN6QBDuc8W5Ilh8o-mNPgOY130 assertion
type: Assertion
description: [Specific interleukin-1 gene polymorphisms in Turkish patients with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15679582
was generated by: ECO_0000203

NP56558.RAbpxHmsk4ZaZhSmpxb2vBdquUsjZEgfV9xs74Ko0kNJY
has assertion: NP56558.RAbpxHmsk4ZaZhSmpxb2vBdquUsjZEgfV9xs74Ko0kNJY130 assertion
has provenance: NP56558.RAbpxHmsk4ZaZhSmpxb2vBdquUsjZEgfV9xs74Ko0kNJY130 provenance
has publication info: NP56558.RAbpxHmsk4ZaZhSmpxb2vBdquUsjZEgfV9xs74Ko0kNJY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56558.RAbpxHmsk4ZaZhSmpxb2vBdquUsjZEgfV9xs74Ko0kNJY130 assertion
type: Assertion
description: [ Diminished cell-mediated immune response, which is controlled genetically, appeared to be an important risk determinant of HBV-related hepatocellular carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15643599
was generated by: ECO_0000203

NP56561.RAa0Hk175FFxDG1XI16MvNuUAVdHatjat5 AH3AG8--Uc
has assertion: NP56561.RAa0Hk175FFxDG1XI16MvNuUAVdHatjat5 AH3AG8--Uc130 assertion
has provenance: NP56561.RAa0Hk175FFxDG1XI16MvNuUAVdHatjat5 AH3AG8--Uc130 provenance
has publication info: NP56561.RAa0Hk175FFxDG1XI16MvNuUAVdHatjat5 AH3AG8--Uc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56561.RAa0Hk175FFxDG1XI16MvNuUAVdHatjat5 AH3AG8--Uc130 assertion
type: Assertion
description: [ Our data suggest an association of genetic variants in IL-6 and IL-2 with hayfever, confirm a role of polymorphisms in IL-4R, IL-13, and IL-18 for the elevated IgE phenotype, and add IL-6 to the list of candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15005726
was generated by: ECO_0000203

NP56564.RAfsW4TQCWMlUp2pv-lV8qLl7MpZbPuLUE 5ErKVGJ6iw
has assertion: NP56564.RAfsW4TQCWMlUp2pv-lV8qLl7MpZbPuLUE 5ErKVGJ6iw130 assertion
has provenance: NP56564.RAfsW4TQCWMlUp2pv-lV8qLl7MpZbPuLUE 5ErKVGJ6iw130 provenance
has publication info: NP56564.RAfsW4TQCWMlUp2pv-lV8qLl7MpZbPuLUE 5ErKVGJ6iw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56564.RAfsW4TQCWMlUp2pv-lV8qLl7MpZbPuLUE 5ErKVGJ6iw130 assertion
type: Assertion
description: [Haplotypes of the IL18 promotor region may contribute to CD risk, consistent with this cytokines role in maintaining inflammation in active CD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20478055
was generated by: ECO_0000203

NP56566.RAcnVkzzhtJc8cQ0Om6doaog50pQjyYS7ER276TPbDOYQ
has assertion: NP56566.RAcnVkzzhtJc8cQ0Om6doaog50pQjyYS7ER276TPbDOYQ130 assertion
has provenance: NP56566.RAcnVkzzhtJc8cQ0Om6doaog50pQjyYS7ER276TPbDOYQ130 provenance
has publication info: NP56566.RAcnVkzzhtJc8cQ0Om6doaog50pQjyYS7ER276TPbDOYQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56566.RAcnVkzzhtJc8cQ0Om6doaog50pQjyYS7ER276TPbDOYQ130 assertion
type: Assertion
description: [Analysis of the data within ethnic subgroups revealed a significant positive association of the heterozygous IL-18 GC genotype with ovarian cancer risk among Native Hawaiian women (OR: 9.96; 95% CI: 1.88-52.90).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15581980
was generated by: ECO_0000203

NP56571.RAY90bQVgf1egmUNs1aiC4cgnMRLxNjfv-flNwFDM4s2M
has assertion: NP56571.RAY90bQVgf1egmUNs1aiC4cgnMRLxNjfv-flNwFDM4s2M130 assertion
has provenance: NP56571.RAY90bQVgf1egmUNs1aiC4cgnMRLxNjfv-flNwFDM4s2M130 provenance
has publication info: NP56571.RAY90bQVgf1egmUNs1aiC4cgnMRLxNjfv-flNwFDM4s2M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56571.RAY90bQVgf1egmUNs1aiC4cgnMRLxNjfv-flNwFDM4s2M130 assertion
type: Assertion
description: [We examined two single nucleotide polymorphisms of the IL-18 gene in 119 patients with sarcoidosis and 130 healthy control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12366781
was generated by: ECO_0000203

NP56576.RAaXiOV4LEQn2-77sRqoy ANU8pOlu5ADxHhN2d9eJW3Q
has assertion: NP56576.RAaXiOV4LEQn2-77sRqoy ANU8pOlu5ADxHhN2d9eJW3Q130 assertion
has provenance: NP56576.RAaXiOV4LEQn2-77sRqoy ANU8pOlu5ADxHhN2d9eJW3Q130 provenance
has publication info: NP56576.RAaXiOV4LEQn2-77sRqoy ANU8pOlu5ADxHhN2d9eJW3Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56576.RAaXiOV4LEQn2-77sRqoy ANU8pOlu5ADxHhN2d9eJW3Q130 assertion
type: Assertion
description: [Association of single nucleotide polymorphism of interleukin-18 with atopic dermatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19453784
was generated by: ECO_0000203

NP56577.RAez6zG8ci0he9sAZLCdG955gTuJNZskGVIgsdw0sDWOM
has assertion: NP56577.RAez6zG8ci0he9sAZLCdG955gTuJNZskGVIgsdw0sDWOM130 assertion
has provenance: NP56577.RAez6zG8ci0he9sAZLCdG955gTuJNZskGVIgsdw0sDWOM130 provenance
has publication info: NP56577.RAez6zG8ci0he9sAZLCdG955gTuJNZskGVIgsdw0sDWOM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56577.RAez6zG8ci0he9sAZLCdG955gTuJNZskGVIgsdw0sDWOM130 assertion
type: Assertion
description: [We showed that the rs438421 polymorphism in the IL-12RB1 (TT) gene and the rs2066446 polymorphism in the IL-12RB2 (AA) gene had a significant interaction to develop the ADe phenotype (allergic type of AD), and those individuals with the risk alleles, TT/AA/CC (IL-12RB1/IL-12RB2/IL-18), have more than a 10-fold increased risk to develop ADe.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20060272
was generated by: ECO_0000203

NP56582.RAZfjn03khT8XHHzKv2hheCzVXHBem0SWRbSpaldzBbRQ
has assertion: NP56582.RAZfjn03khT8XHHzKv2hheCzVXHBem0SWRbSpaldzBbRQ130 assertion
has provenance: NP56582.RAZfjn03khT8XHHzKv2hheCzVXHBem0SWRbSpaldzBbRQ130 provenance
has publication info: NP56582.RAZfjn03khT8XHHzKv2hheCzVXHBem0SWRbSpaldzBbRQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56582.RAZfjn03khT8XHHzKv2hheCzVXHBem0SWRbSpaldzBbRQ130 assertion
type: Assertion
description: [Here, we investigated whether interleukin (IL)-18 single nucleotide polymorphisms (SNPs) are involved in Chinese asthma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18200581
was generated by: ECO_0000203

NP56584.RAa9PGk8Dnyc10U FMHJIGtmwe8yIJCzVBYHaBiWrvj6M
has assertion: NP56584.RAa9PGk8Dnyc10U FMHJIGtmwe8yIJCzVBYHaBiWrvj6M130 assertion
has provenance: NP56584.RAa9PGk8Dnyc10U FMHJIGtmwe8yIJCzVBYHaBiWrvj6M130 provenance
has publication info: NP56584.RAa9PGk8Dnyc10U FMHJIGtmwe8yIJCzVBYHaBiWrvj6M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56584.RAa9PGk8Dnyc10U FMHJIGtmwe8yIJCzVBYHaBiWrvj6M130 assertion
type: Assertion
description: [Interleukin-18 promoter polymorphisms and the disease progression of Hepatitis B virus-related liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19138654
was generated by: ECO_0000203

NP56585.RAQTldHRicNqLfcu329NveiIKgjtUrThfa3ZQAbVNqRp8
has assertion: NP56585.RAQTldHRicNqLfcu329NveiIKgjtUrThfa3ZQAbVNqRp8130 assertion
has provenance: NP56585.RAQTldHRicNqLfcu329NveiIKgjtUrThfa3ZQAbVNqRp8130 provenance
has publication info: NP56585.RAQTldHRicNqLfcu329NveiIKgjtUrThfa3ZQAbVNqRp8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56585.RAQTldHRicNqLfcu329NveiIKgjtUrThfa3ZQAbVNqRp8130 assertion
type: Assertion
description: [Disease association of two distinct interleukin-18 promoter polymorphisms in Caucasian rheumatoid arthritis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15789055
was generated by: ECO_0000203

NP56591.RAefIUHOaoQCZykLTsQoE35i9dWEHT1O-3wY3hNydF1EY
has assertion: NP56591.RAefIUHOaoQCZykLTsQoE35i9dWEHT1O-3wY3hNydF1EY130 assertion
has provenance: NP56591.RAefIUHOaoQCZykLTsQoE35i9dWEHT1O-3wY3hNydF1EY130 provenance
has publication info: NP56591.RAefIUHOaoQCZykLTsQoE35i9dWEHT1O-3wY3hNydF1EY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56591.RAefIUHOaoQCZykLTsQoE35i9dWEHT1O-3wY3hNydF1EY130 assertion
type: Assertion
description: [Prevalence of the -295 T-to-C promoter polymorphism of the interleukin (IL)-16 gene in periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16178875
was generated by: ECO_0000203

NP56594.RAbXidPctCGnkXoUv7Jkctv4gjSxMqi1xEjW6SfIfdHnA
has assertion: NP56594.RAbXidPctCGnkXoUv7Jkctv4gjSxMqi1xEjW6SfIfdHnA130 assertion
has provenance: NP56594.RAbXidPctCGnkXoUv7Jkctv4gjSxMqi1xEjW6SfIfdHnA130 provenance
has publication info: NP56594.RAbXidPctCGnkXoUv7Jkctv4gjSxMqi1xEjW6SfIfdHnA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56594.RAbXidPctCGnkXoUv7Jkctv4gjSxMqi1xEjW6SfIfdHnA130 assertion
type: Assertion
description: [Genetic approaches to the investigation of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11981324
was generated by: ECO_0000203

NP56601.RAUOtwqPht0g JT9 RZYGUiPn4rYxBNQ3g-aEu3KLlzyk
has assertion: NP56601.RAUOtwqPht0g JT9 RZYGUiPn4rYxBNQ3g-aEu3KLlzyk130 assertion
has provenance: NP56601.RAUOtwqPht0g JT9 RZYGUiPn4rYxBNQ3g-aEu3KLlzyk130 provenance
has publication info: NP56601.RAUOtwqPht0g JT9 RZYGUiPn4rYxBNQ3g-aEu3KLlzyk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56601.RAUOtwqPht0g JT9 RZYGUiPn4rYxBNQ3g-aEu3KLlzyk130 assertion
type: Assertion
description: [ These findings suggest that variants C-1055T and Arg130Gln of the IL13 gene might play an important role on total serum IgE production in this study population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12897746
was generated by: ECO_0000203

NP56606.RAYy3zxpK0EjqVwRWFwOhChW3RKY-Ogz6ZwEpqiMOsE3s
has assertion: NP56606.RAYy3zxpK0EjqVwRWFwOhChW3RKY-Ogz6ZwEpqiMOsE3s130 assertion
has provenance: NP56606.RAYy3zxpK0EjqVwRWFwOhChW3RKY-Ogz6ZwEpqiMOsE3s130 provenance
has publication info: NP56606.RAYy3zxpK0EjqVwRWFwOhChW3RKY-Ogz6ZwEpqiMOsE3s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56606.RAYy3zxpK0EjqVwRWFwOhChW3RKY-Ogz6ZwEpqiMOsE3s130 assertion
type: Assertion
description: [Several interleukin-4 and interleukin-13 gene single nucleotide polymorphisms among Chinese asthmatic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19772762
was generated by: ECO_0000203

NP56614.RAXTr HUTmJLRFx1q4-H9R mkds6ISlQsJaZTWWZwDEpY
has assertion: NP56614.RAXTr HUTmJLRFx1q4-H9R mkds6ISlQsJaZTWWZwDEpY130 assertion
has provenance: NP56614.RAXTr HUTmJLRFx1q4-H9R mkds6ISlQsJaZTWWZwDEpY130 provenance
has publication info: NP56614.RAXTr HUTmJLRFx1q4-H9R mkds6ISlQsJaZTWWZwDEpY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56614.RAXTr HUTmJLRFx1q4-H9R mkds6ISlQsJaZTWWZwDEpY130 assertion
type: Assertion
description: [We further identified that asthmatic patients homozygous for the Gln110 variant have higher serum levels of IL-13 than those without the variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12063528
was generated by: ECO_0000203

NP56622.RAVbmOxC uAtisNHsPZ8Y7gSUIi1G5nQp1-PXh011gv8Q
has assertion: NP56622.RAVbmOxC uAtisNHsPZ8Y7gSUIi1G5nQp1-PXh011gv8Q130 assertion
has provenance: NP56622.RAVbmOxC uAtisNHsPZ8Y7gSUIi1G5nQp1-PXh011gv8Q130 provenance
has publication info: NP56622.RAVbmOxC uAtisNHsPZ8Y7gSUIi1G5nQp1-PXh011gv8Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56622.RAVbmOxC uAtisNHsPZ8Y7gSUIi1G5nQp1-PXh011gv8Q130 assertion
type: Assertion
description: [The odds ratios (ORs) for the association between IL-2 polymorphism OR = 2.78, 95% CI (confidence interval) = 1.26-6.17 (T/T to G/G) or IL-4 polymorphism OR = 2.22, 95% CI = 1.01-4.89 (T/C to C/C) were increased significantly with gastric atrophy, whereas the corresponding OR of IL-13 polymorphism was decreased with gastric atrophy OR = 0.61, 95% CI = 0.39-0.96 (C/T and T/T to C/C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15904474
was generated by: ECO_0000203

NP56623.RAQm0nP2Rmk XwnB b-Z5 CsvR2UM7rIl66XTV2Rb FsU
has assertion: NP56623.RAQm0nP2Rmk XwnB b-Z5 CsvR2UM7rIl66XTV2Rb FsU130 assertion
has provenance: NP56623.RAQm0nP2Rmk XwnB b-Z5 CsvR2UM7rIl66XTV2Rb FsU130 provenance
has publication info: NP56623.RAQm0nP2Rmk XwnB b-Z5 CsvR2UM7rIl66XTV2Rb FsU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56623.RAQm0nP2Rmk XwnB b-Z5 CsvR2UM7rIl66XTV2Rb FsU130 assertion
type: Assertion
description: [These results suggest that genetic polymorphisms in the 3'UTR of the IL-13 gene correlate with long-term outcome of MCNS, rather than disease susceptibility, in Singapore Chinese children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15728267
was generated by: ECO_0000203

NP56627.RAUu1oTIBDVmvT9vhQMyMS6 y-AKZb1TB7GgtdkODuBoY
has assertion: NP56627.RAUu1oTIBDVmvT9vhQMyMS6 y-AKZb1TB7GgtdkODuBoY130 assertion
has provenance: NP56627.RAUu1oTIBDVmvT9vhQMyMS6 y-AKZb1TB7GgtdkODuBoY130 provenance
has publication info: NP56627.RAUu1oTIBDVmvT9vhQMyMS6 y-AKZb1TB7GgtdkODuBoY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56627.RAUu1oTIBDVmvT9vhQMyMS6 y-AKZb1TB7GgtdkODuBoY130 assertion
type: Assertion
description: [Thus, our results suggest a possible involvement of IL-13 SNPs in the regulation of IgE production in response to allergens in this Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12928861
was generated by: ECO_0000203

NP56628.RATkQAE2DjbAZZU32H5QbJZsPZ9RVST2OLbkCPY72OwvE
has assertion: NP56628.RATkQAE2DjbAZZU32H5QbJZsPZ9RVST2OLbkCPY72OwvE130 assertion
has provenance: NP56628.RATkQAE2DjbAZZU32H5QbJZsPZ9RVST2OLbkCPY72OwvE130 provenance
has publication info: NP56628.RATkQAE2DjbAZZU32H5QbJZsPZ9RVST2OLbkCPY72OwvE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56628.RATkQAE2DjbAZZU32H5QbJZsPZ9RVST2OLbkCPY72OwvE130 assertion
type: Assertion
description: [Polymorphisms in the IL-13 and IL-4 receptor alpha genes and allergic rhinitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17091279
was generated by: ECO_0000203

NP56632.RAfcJ-HO4Qx3ej3KipZy8otm-ye6VfM7GBL58E90ruC 0
has assertion: NP56632.RAfcJ-HO4Qx3ej3KipZy8otm-ye6VfM7GBL58E90ruC 0130 assertion
has provenance: NP56632.RAfcJ-HO4Qx3ej3KipZy8otm-ye6VfM7GBL58E90ruC 0130 provenance
has publication info: NP56632.RAfcJ-HO4Qx3ej3KipZy8otm-ye6VfM7GBL58E90ruC 0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56632.RAfcJ-HO4Qx3ej3KipZy8otm-ye6VfM7GBL58E90ruC 0130 assertion
type: Assertion
description: [An IL-13 promoter polymorphism associated with increased risk of allergic asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11197307
was generated by: ECO_0000203

NP56641.RAV8yQ5HrJ9s0sYiqunLgvi5EpvhYEUXjhBbfD34sVtdQ
has assertion: NP56641.RAV8yQ5HrJ9s0sYiqunLgvi5EpvhYEUXjhBbfD34sVtdQ130 assertion
has provenance: NP56641.RAV8yQ5HrJ9s0sYiqunLgvi5EpvhYEUXjhBbfD34sVtdQ130 provenance
has publication info: NP56641.RAV8yQ5HrJ9s0sYiqunLgvi5EpvhYEUXjhBbfD34sVtdQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56641.RAV8yQ5HrJ9s0sYiqunLgvi5EpvhYEUXjhBbfD34sVtdQ130 assertion
type: Assertion
description: [Our aim was to assess relation between an IL12B promoter polymorphism and asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12241719
was generated by: ECO_0000203

NP56642.RAcSb4H5Ch3PmtowULh4F WNHf6qbS8NLzosDPwCXCl8k
has assertion: NP56642.RAcSb4H5Ch3PmtowULh4F WNHf6qbS8NLzosDPwCXCl8k130 assertion
has provenance: NP56642.RAcSb4H5Ch3PmtowULh4F WNHf6qbS8NLzosDPwCXCl8k130 provenance
has publication info: NP56642.RAcSb4H5Ch3PmtowULh4F WNHf6qbS8NLzosDPwCXCl8k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56642.RAcSb4H5Ch3PmtowULh4F WNHf6qbS8NLzosDPwCXCl8k130 assertion
type: Assertion
description: [ In this long-term study of asthmatic subjects with comprehensive data on asthma severity, we found no evidence to support the presence of a heterozygote effect of the IL12B promoter polymorphism on the level of asthma in early childhood or adulthood. The polymorphism was also not associated with asthma susceptibility, but the CTCTAA allele may have been associated with elevated serum IgE levels in male subjects and reduced pulmonary function in female subjects in early childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15007350
was generated by: ECO_0000203

NP56645.RAQUgW1A1Fc0CNi5OZCrbwxdYvLNYYpuhgnxFh57ESsq8
has assertion: NP56645.RAQUgW1A1Fc0CNi5OZCrbwxdYvLNYYpuhgnxFh57ESsq8130 assertion
has provenance: NP56645.RAQUgW1A1Fc0CNi5OZCrbwxdYvLNYYpuhgnxFh57ESsq8130 provenance
has publication info: NP56645.RAQUgW1A1Fc0CNi5OZCrbwxdYvLNYYpuhgnxFh57ESsq8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56645.RAQUgW1A1Fc0CNi5OZCrbwxdYvLNYYpuhgnxFh57ESsq8130 assertion
type: Assertion
description: [Replication of genetic association studies in asthma and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20395963
was generated by: ECO_0000203

NP56648.RAXaBeEtACvHTCmIxNtUFB3q23-7rHbpCaK-3YnrdpMPQ
has assertion: NP56648.RAXaBeEtACvHTCmIxNtUFB3q23-7rHbpCaK-3YnrdpMPQ130 assertion
has provenance: NP56648.RAXaBeEtACvHTCmIxNtUFB3q23-7rHbpCaK-3YnrdpMPQ130 provenance
has publication info: NP56648.RAXaBeEtACvHTCmIxNtUFB3q23-7rHbpCaK-3YnrdpMPQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56648.RAXaBeEtACvHTCmIxNtUFB3q23-7rHbpCaK-3YnrdpMPQ130 assertion
type: Assertion
description: [Our findings support the concept that an individual's genetically determined ability to produce IL-12 is another factor that can influence the outcome of HCV infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15871664
was generated by: ECO_0000203

NP56649.RAQny5YQJWjiXd8msc4pJgSVTa2yujx7dKVq4e00o2eDU
has assertion: NP56649.RAQny5YQJWjiXd8msc4pJgSVTa2yujx7dKVq4e00o2eDU130 assertion
has provenance: NP56649.RAQny5YQJWjiXd8msc4pJgSVTa2yujx7dKVq4e00o2eDU130 provenance
has publication info: NP56649.RAQny5YQJWjiXd8msc4pJgSVTa2yujx7dKVq4e00o2eDU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56649.RAQny5YQJWjiXd8msc4pJgSVTa2yujx7dKVq4e00o2eDU130 assertion
type: Assertion
description: [Associations between IL12B polymorphisms and tuberculosis in the Hong Kong Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15295696
was generated by: ECO_0000203

NP56652.RAYi42nkIoA42jXHD-BYQonXptAo4jkV2pA3ZYybnejx0
has assertion: NP56652.RAYi42nkIoA42jXHD-BYQonXptAo4jkV2pA3ZYybnejx0130 assertion
has provenance: NP56652.RAYi42nkIoA42jXHD-BYQonXptAo4jkV2pA3ZYybnejx0130 provenance
has publication info: NP56652.RAYi42nkIoA42jXHD-BYQonXptAo4jkV2pA3ZYybnejx0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56652.RAYi42nkIoA42jXHD-BYQonXptAo4jkV2pA3ZYybnejx0130 assertion
type: Assertion
description: [Interestingly, IL12B promoter heterozygosity was associated with protection from tuberculosis in BCG-vaccinated individuals (p=0.03; OR=0.6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17392024
was generated by: ECO_0000203

NP56659.RAbcM-UR1I-NvrxbYXz1RrmnzdcnSwSdtqehQ5hSYzC o
has assertion: NP56659.RAbcM-UR1I-NvrxbYXz1RrmnzdcnSwSdtqehQ5hSYzC o130 assertion
has provenance: NP56659.RAbcM-UR1I-NvrxbYXz1RrmnzdcnSwSdtqehQ5hSYzC o130 provenance
has publication info: NP56659.RAbcM-UR1I-NvrxbYXz1RrmnzdcnSwSdtqehQ5hSYzC o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56659.RAbcM-UR1I-NvrxbYXz1RrmnzdcnSwSdtqehQ5hSYzC o130 assertion
type: Assertion
description: [Interleukin-12 p40 gene (IL12B) 3'-untranslated region polymorphism is associated with susceptibility to atopic dermatitis and psoriasis vulgaris.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12413772
was generated by: ECO_0000203

NP56660.RAVDed5QnwmB8j7x84Jt3rYGaOZOa DNv-I X78FdYhDU
has assertion: NP56660.RAVDed5QnwmB8j7x84Jt3rYGaOZOa DNv-I X78FdYhDU130 assertion
has provenance: NP56660.RAVDed5QnwmB8j7x84Jt3rYGaOZOa DNv-I X78FdYhDU130 provenance
has publication info: NP56660.RAVDed5QnwmB8j7x84Jt3rYGaOZOa DNv-I X78FdYhDU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56660.RAVDed5QnwmB8j7x84Jt3rYGaOZOa DNv-I X78FdYhDU130 assertion
type: Assertion
description: [A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17236132
was generated by: ECO_0000203

NP56664.RAZ5h2B3wfJewLRJZPgsI P3BKqO8EJOIXNGm1v9TXkFg
has assertion: NP56664.RAZ5h2B3wfJewLRJZPgsI P3BKqO8EJOIXNGm1v9TXkFg130 assertion
has provenance: NP56664.RAZ5h2B3wfJewLRJZPgsI P3BKqO8EJOIXNGm1v9TXkFg130 provenance
has publication info: NP56664.RAZ5h2B3wfJewLRJZPgsI P3BKqO8EJOIXNGm1v9TXkFg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56664.RAZ5h2B3wfJewLRJZPgsI P3BKqO8EJOIXNGm1v9TXkFg130 assertion
type: Assertion
description: [Polymorphisms of the IL12B and IL23R genes are associated with psoriasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18219280
was generated by: ECO_0000203

NP56665.RASAUmDqVbqnDNzAKZtTHC0cSNMPB4ZWaPgJ35fW3pj5c
has assertion: NP56665.RASAUmDqVbqnDNzAKZtTHC0cSNMPB4ZWaPgJ35fW3pj5c130 assertion
has provenance: NP56665.RASAUmDqVbqnDNzAKZtTHC0cSNMPB4ZWaPgJ35fW3pj5c130 provenance
has publication info: NP56665.RASAUmDqVbqnDNzAKZtTHC0cSNMPB4ZWaPgJ35fW3pj5c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56665.RASAUmDqVbqnDNzAKZtTHC0cSNMPB4ZWaPgJ35fW3pj5c130 assertion
type: Assertion
description: [Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20953188
was generated by: ECO_0000203

NP56671.RARbUzBk6lNi4 oLC8kzPDsHxEN3m6MvVa8PfdOt0Qyn4
has assertion: NP56671.RARbUzBk6lNi4 oLC8kzPDsHxEN3m6MvVa8PfdOt0Qyn4130 assertion
has provenance: NP56671.RARbUzBk6lNi4 oLC8kzPDsHxEN3m6MvVa8PfdOt0Qyn4130 provenance
has publication info: NP56671.RARbUzBk6lNi4 oLC8kzPDsHxEN3m6MvVa8PfdOt0Qyn4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56671.RARbUzBk6lNi4 oLC8kzPDsHxEN3m6MvVa8PfdOt0Qyn4130 assertion
type: Assertion
description: [These findings suggest that - with the possible exception of IL-1beta- genetic variation associated with differential expression of the selected pro- and anti-inflammatory cytokines is unlikely to play a major role in susceptibility to and prognosis in CMM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14675394
was generated by: ECO_0000203

NP56675.RAd71n1DdYsRSvNch9sFaq 1oX9VkHTtbyTGj7Mwos-n8
has assertion: NP56675.RAd71n1DdYsRSvNch9sFaq 1oX9VkHTtbyTGj7Mwos-n8130 assertion
has provenance: NP56675.RAd71n1DdYsRSvNch9sFaq 1oX9VkHTtbyTGj7Mwos-n8130 provenance
has publication info: NP56675.RAd71n1DdYsRSvNch9sFaq 1oX9VkHTtbyTGj7Mwos-n8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56675.RAd71n1DdYsRSvNch9sFaq 1oX9VkHTtbyTGj7Mwos-n8130 assertion
type: Assertion
description: [IL-10, TGF-beta, IL-2, IL-12, and IFN-gamma cytokine gene polymorphisms in asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18972297
was generated by: ECO_0000203

NP56683.RAfqOKpuhfCD6LX5k5wP82sCmMWqkEyKrvpswgGpgsvGk
has assertion: NP56683.RAfqOKpuhfCD6LX5k5wP82sCmMWqkEyKrvpswgGpgsvGk130 assertion
has provenance: NP56683.RAfqOKpuhfCD6LX5k5wP82sCmMWqkEyKrvpswgGpgsvGk130 provenance
has publication info: NP56683.RAfqOKpuhfCD6LX5k5wP82sCmMWqkEyKrvpswgGpgsvGk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56683.RAfqOKpuhfCD6LX5k5wP82sCmMWqkEyKrvpswgGpgsvGk130 assertion
type: Assertion
description: [The chromosome 21q22.11 cytokine receptor cluster contains four genes that encode subunits of the receptors for the cytokines interleukin-10 and interferon-alpha, -beta and -gamma that may have a role in malaria pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12761564
was generated by: ECO_0000203

NP56687.RAb-vOiutTQ1fGZBVgN7Xa--C4AvMwUldFc77k1J2h-BQ
has assertion: NP56687.RAb-vOiutTQ1fGZBVgN7Xa--C4AvMwUldFc77k1J2h-BQ130 assertion
has provenance: NP56687.RAb-vOiutTQ1fGZBVgN7Xa--C4AvMwUldFc77k1J2h-BQ130 provenance
has publication info: NP56687.RAb-vOiutTQ1fGZBVgN7Xa--C4AvMwUldFc77k1J2h-BQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56687.RAb-vOiutTQ1fGZBVgN7Xa--C4AvMwUldFc77k1J2h-BQ130 assertion
type: Assertion
description: [Microsatellites (MS) at positions -4000 and -1200 (IL10R and IL10G, respectively) and single nucleotide polymorphisms (SNPs) (MS) at positions -1082G/A, -819C/T and -592C/A of the IL-10 promoter were analysed in patients with SLE and healthy controls from Canary Islands (Spain).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18397303
was generated by: ECO_0000203

NP56688.RAf2yF-2KKz6FOCKVSxrmPwB w2jq5nOBPW3MQHf3-yuc
has assertion: NP56688.RAf2yF-2KKz6FOCKVSxrmPwB w2jq5nOBPW3MQHf3-yuc130 assertion
has provenance: NP56688.RAf2yF-2KKz6FOCKVSxrmPwB w2jq5nOBPW3MQHf3-yuc130 provenance
has publication info: NP56688.RAf2yF-2KKz6FOCKVSxrmPwB w2jq5nOBPW3MQHf3-yuc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56688.RAf2yF-2KKz6FOCKVSxrmPwB w2jq5nOBPW3MQHf3-yuc130 assertion
type: Assertion
description: [The analysis of combined genotypes of the studied genes suggests a synergic action of genes Fc gamma RIIIA and IL-10 on the risk to develop SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12847896
was generated by: ECO_0000203

NP56689.RATt8 c0yxu0zgJJEUmBC3pk7JQcHYKcXD0zIj5h7aKFo
has assertion: NP56689.RATt8 c0yxu0zgJJEUmBC3pk7JQcHYKcXD0zIj5h7aKFo130 assertion
has provenance: NP56689.RATt8 c0yxu0zgJJEUmBC3pk7JQcHYKcXD0zIj5h7aKFo130 provenance
has publication info: NP56689.RATt8 c0yxu0zgJJEUmBC3pk7JQcHYKcXD0zIj5h7aKFo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56689.RATt8 c0yxu0zgJJEUmBC3pk7JQcHYKcXD0zIj5h7aKFo130 assertion
type: Assertion
description: [Novel single nucleotide polymorphisms in the distal IL-10 promoter affect IL-10 production and enhance the risk of systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11238636
was generated by: ECO_0000203

NP56690.RAXJZ9vUMT4k6O0Zg4k0AyQQCbFzyYD3sCQkV7tQDAvoQ
has assertion: NP56690.RAXJZ9vUMT4k6O0Zg4k0AyQQCbFzyYD3sCQkV7tQDAvoQ130 assertion
has provenance: NP56690.RAXJZ9vUMT4k6O0Zg4k0AyQQCbFzyYD3sCQkV7tQDAvoQ130 provenance
has publication info: NP56690.RAXJZ9vUMT4k6O0Zg4k0AyQQCbFzyYD3sCQkV7tQDAvoQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56690.RAXJZ9vUMT4k6O0Zg4k0AyQQCbFzyYD3sCQkV7tQDAvoQ130 assertion
type: Assertion
description: [A significant increase was found in SLE patients (0.170 versus 0.095; chi2y = 4.11, P = 0.0425) in the frequency of the 140-basepair allele of the IL10.G microsatellite located in the promoter region of the IL-10 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10643707
was generated by: ECO_0000203

NP56692.RAecOXNJGKBGgLMMDcBcyN4BP5GHmgoHLRbrJVlNVruvQ
has assertion: NP56692.RAecOXNJGKBGgLMMDcBcyN4BP5GHmgoHLRbrJVlNVruvQ130 assertion
has provenance: NP56692.RAecOXNJGKBGgLMMDcBcyN4BP5GHmgoHLRbrJVlNVruvQ130 provenance
has publication info: NP56692.RAecOXNJGKBGgLMMDcBcyN4BP5GHmgoHLRbrJVlNVruvQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56692.RAecOXNJGKBGgLMMDcBcyN4BP5GHmgoHLRbrJVlNVruvQ130 assertion
type: Assertion
description: [DNA from 76 Caucasian patients with SLE and 119 controls as genotyped for 3 defined dimorphic polymorphisms (G or A at position -1082, C or T at position -819, C or A at position -592) in the promoter region of the IL-10 gene, using the polymerase chain reaction to amplify the IL-10 gene promoter and oligonucleotide probes specific for each allelic sequence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9415634
was generated by: ECO_0000203

NP56693.RAUeq7l8h2lxmIDAWM6rSm6r5GRo7llsCH0QgIgRhXHjw
has assertion: NP56693.RAUeq7l8h2lxmIDAWM6rSm6r5GRo7llsCH0QgIgRhXHjw130 assertion
has provenance: NP56693.RAUeq7l8h2lxmIDAWM6rSm6r5GRo7llsCH0QgIgRhXHjw130 provenance
has publication info: NP56693.RAUeq7l8h2lxmIDAWM6rSm6r5GRo7llsCH0QgIgRhXHjw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56693.RAUeq7l8h2lxmIDAWM6rSm6r5GRo7llsCH0QgIgRhXHjw130 assertion
type: Assertion
description: [Recent studies have shown elevated IL-10 levels in several rheumatic autoimmune diseases, and particularly in systemic lupus erythematosus (SLE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9234486
was generated by: ECO_0000203

NP56695.RASf9UCzAtFYIqvR7asy7EyEFQfUQ6el9ylINvynuiBSY
has assertion: NP56695.RASf9UCzAtFYIqvR7asy7EyEFQfUQ6el9ylINvynuiBSY130 assertion
has provenance: NP56695.RASf9UCzAtFYIqvR7asy7EyEFQfUQ6el9ylINvynuiBSY130 provenance
has publication info: NP56695.RASf9UCzAtFYIqvR7asy7EyEFQfUQ6el9ylINvynuiBSY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56695.RASf9UCzAtFYIqvR7asy7EyEFQfUQ6el9ylINvynuiBSY130 assertion
type: Assertion
description: [ These findings suggest an association between the genetic ability to produce low levels of IFN-gamma and the susceptibility to develop chronic HBV infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12526950
was generated by: ECO_0000203

NP56696.RAZGodq2Gc6NKx3-SxcMNaK4iTEQRgFKTKh8Qy4F5PtgA
has assertion: NP56696.RAZGodq2Gc6NKx3-SxcMNaK4iTEQRgFKTKh8Qy4F5PtgA130 assertion
has provenance: NP56696.RAZGodq2Gc6NKx3-SxcMNaK4iTEQRgFKTKh8Qy4F5PtgA130 provenance
has publication info: NP56696.RAZGodq2Gc6NKx3-SxcMNaK4iTEQRgFKTKh8Qy4F5PtgA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56696.RAZGodq2Gc6NKx3-SxcMNaK4iTEQRgFKTKh8Qy4F5PtgA130 assertion
type: Assertion
description: [There was no evident relationship between IL-4-590 C/T allele SNP and susceptibility to HBV intrauterine infection, but the IL-10-1082 G allele seemed to be associated with preventive efficacy to HBV intrauterine infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15941525
was generated by: ECO_0000203

NP56698.RAUugN4Rkrfx4x2KQCb mlxa4SmqUZmoPydStLZ9UzAlI
has assertion: NP56698.RAUugN4Rkrfx4x2KQCb mlxa4SmqUZmoPydStLZ9UzAlI130 assertion
has provenance: NP56698.RAUugN4Rkrfx4x2KQCb mlxa4SmqUZmoPydStLZ9UzAlI130 provenance
has publication info: NP56698.RAUugN4Rkrfx4x2KQCb mlxa4SmqUZmoPydStLZ9UzAlI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56698.RAUugN4Rkrfx4x2KQCb mlxa4SmqUZmoPydStLZ9UzAlI130 assertion
type: Assertion
description: [Association of cytokine genetic polymorphism with hepatitis B infection evolution in adult patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17612762
was generated by: ECO_0000203

NP56704.RAQ2JrxohIshpyb247U4ZuLoUZ5I4umaCZ1C6bXpE8T9k
has assertion: NP56704.RAQ2JrxohIshpyb247U4ZuLoUZ5I4umaCZ1C6bXpE8T9k130 assertion
has provenance: NP56704.RAQ2JrxohIshpyb247U4ZuLoUZ5I4umaCZ1C6bXpE8T9k130 provenance
has publication info: NP56704.RAQ2JrxohIshpyb247U4ZuLoUZ5I4umaCZ1C6bXpE8T9k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56704.RAQ2JrxohIshpyb247U4ZuLoUZ5I4umaCZ1C6bXpE8T9k130 assertion
type: Assertion
description: [Chagas' disease susceptibility/resistance: linkage disequilibrium analysis suggests epistasis between major histocompatibility complex and interleukin-10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15191519
was generated by: ECO_0000203

NP56705.RAeLWl-dJc aQ55mMKJB61pPxcZ1m6TAa53tzTNMAMMtE
has assertion: NP56705.RAeLWl-dJc aQ55mMKJB61pPxcZ1m6TAa53tzTNMAMMtE130 assertion
has provenance: NP56705.RAeLWl-dJc aQ55mMKJB61pPxcZ1m6TAa53tzTNMAMMtE130 provenance
has publication info: NP56705.RAeLWl-dJc aQ55mMKJB61pPxcZ1m6TAa53tzTNMAMMtE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56705.RAeLWl-dJc aQ55mMKJB61pPxcZ1m6TAa53tzTNMAMMtE130 assertion
type: Assertion
description: [Single nucleotide polymorphisms and intragenic microsatellite markers within 8 candidate cytokine genes (interleukin-1alpha IL-1alpha, IL-2, IL-4, IL-6, IL-10, interferon-alpha1 IFNA1, interferon-gamma IFNG, and interferon regulatory factor 1 IRF-1) were investigated in 417 Caucasian patients with clinically characterized JIA and a panel of 276 unrelated, healthy Caucasian controls, all from the United Kingdom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11315919
was generated by: ECO_0000203

NP56713.RARoPiRiYy2HKrBGhch0k1sBjSOUUv59vQ8GLeCJ6EtOs
has assertion: NP56713.RARoPiRiYy2HKrBGhch0k1sBjSOUUv59vQ8GLeCJ6EtOs130 assertion
has provenance: NP56713.RARoPiRiYy2HKrBGhch0k1sBjSOUUv59vQ8GLeCJ6EtOs130 provenance
has publication info: NP56713.RARoPiRiYy2HKrBGhch0k1sBjSOUUv59vQ8GLeCJ6EtOs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56713.RARoPiRiYy2HKrBGhch0k1sBjSOUUv59vQ8GLeCJ6EtOs130 assertion
type: Assertion
description: [Role of non-HLA genetic polymorphisms in graft-versus-host disease after haematopoietic stem cell transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16984283
was generated by: ECO_0000203

NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR 67jvT-p3d3sU54
has assertion: NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR 67jvT-p3d3sU54130 assertion
has provenance: NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR 67jvT-p3d3sU54130 provenance
has publication info: NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR 67jvT-p3d3sU54130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR 67jvT-p3d3sU54130 assertion
type: Assertion
description: [ Allele A of the Hsp70-2 gene may be associated with a less severe form of CD, suggesting the clinical value of the genotype assessment. The genetic determination of the defense mechanisms in CD appears to be associated with the polymorphism of the Hsp70-2 gene rather than that of the CD14 or IL-10 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16165702
was generated by: ECO_0000203

NP56724.RATCLS3j7GOHkFJMKu-jMSSKSjsH6Dwk68nGEAurdAU-0
has assertion: NP56724.RATCLS3j7GOHkFJMKu-jMSSKSjsH6Dwk68nGEAurdAU-0130 assertion
has provenance: NP56724.RATCLS3j7GOHkFJMKu-jMSSKSjsH6Dwk68nGEAurdAU-0130 provenance
has publication info: NP56724.RATCLS3j7GOHkFJMKu-jMSSKSjsH6Dwk68nGEAurdAU-0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56724.RATCLS3j7GOHkFJMKu-jMSSKSjsH6Dwk68nGEAurdAU-0130 assertion
type: Assertion
description: [ Our study showed association with JIA for the IL-4 -1098 T/G polymorphism. It also underlines the genetic contribution of IL-1 polymorphisms to the pathogenesis of JIA, as another polymorphism within the IL-1beta may influence the risk of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15170937
was generated by: ECO_0000203

NP56725.RAfvEWDwFjWfvAFpqhAN6JM cfe0d-91NyRGLff9yYNks
has assertion: NP56725.RAfvEWDwFjWfvAFpqhAN6JM cfe0d-91NyRGLff9yYNks130 assertion
has provenance: NP56725.RAfvEWDwFjWfvAFpqhAN6JM cfe0d-91NyRGLff9yYNks130 provenance
has publication info: NP56725.RAfvEWDwFjWfvAFpqhAN6JM cfe0d-91NyRGLff9yYNks130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56725.RAfvEWDwFjWfvAFpqhAN6JM cfe0d-91NyRGLff9yYNks130 assertion
type: Assertion
description: [Juvenile idiopathic arthritis genetics - what's new? What's next?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12223104
was generated by: ECO_0000203

NP56733.RAfo MmJlut4DpcazCc3qWeIAUAyfbtNFa5nhI4jn7Fhg
has assertion: NP56733.RAfo MmJlut4DpcazCc3qWeIAUAyfbtNFa5nhI4jn7Fhg130 assertion
has provenance: NP56733.RAfo MmJlut4DpcazCc3qWeIAUAyfbtNFa5nhI4jn7Fhg130 provenance
has publication info: NP56733.RAfo MmJlut4DpcazCc3qWeIAUAyfbtNFa5nhI4jn7Fhg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56733.RAfo MmJlut4DpcazCc3qWeIAUAyfbtNFa5nhI4jn7Fhg130 assertion
type: Assertion
description: [The ATA (a non-GCC) haplotype, which is associated with low IL-10 expression, has been shown to improve interferon (IFN) treatment response in hepatitis C. We analysed the distribution of IL-10 promoter haplotype combinations to determine whether they could influence initial IFN treatment response in 63 patients with relapsing-remitting multiple sclerosis (MS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15693804
was generated by: ECO_0000203

NP56737.RAX Cu1lUHWGPZ 2B28DuurIRVa4AUE837lFEe0dePPfU
has assertion: NP56737.RAX Cu1lUHWGPZ 2B28DuurIRVa4AUE837lFEe0dePPfU130 assertion
has provenance: NP56737.RAX Cu1lUHWGPZ 2B28DuurIRVa4AUE837lFEe0dePPfU130 provenance
has publication info: NP56737.RAX Cu1lUHWGPZ 2B28DuurIRVa4AUE837lFEe0dePPfU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56737.RAX Cu1lUHWGPZ 2B28DuurIRVa4AUE837lFEe0dePPfU130 assertion
type: Assertion
description: [As a non-European patient population, according to our results, IL10 polymorphism is not associated with MS and its subtypes nor influences the disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20714960
was generated by: ECO_0000203

NP56739.RAUp s9yxZgu kjkheaQFCw LEq5rcMf0AgOyEBTbc2gU
has assertion: NP56739.RAUp s9yxZgu kjkheaQFCw LEq5rcMf0AgOyEBTbc2gU130 assertion
has provenance: NP56739.RAUp s9yxZgu kjkheaQFCw LEq5rcMf0AgOyEBTbc2gU130 provenance
has publication info: NP56739.RAUp s9yxZgu kjkheaQFCw LEq5rcMf0AgOyEBTbc2gU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56739.RAUp s9yxZgu kjkheaQFCw LEq5rcMf0AgOyEBTbc2gU130 assertion
type: Assertion
description: [Genetic polymorphisms, their allele combinations and IFN-beta treatment response in Irish multiple sclerosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19604093
was generated by: ECO_0000203

NP56746.RAeAxa3cbCCNlzDM4LQtUxDl5sBL mjS7FpfkvXVWZ1ws
has assertion: NP56746.RAeAxa3cbCCNlzDM4LQtUxDl5sBL mjS7FpfkvXVWZ1ws130 assertion
has provenance: NP56746.RAeAxa3cbCCNlzDM4LQtUxDl5sBL mjS7FpfkvXVWZ1ws130 provenance
has publication info: NP56746.RAeAxa3cbCCNlzDM4LQtUxDl5sBL mjS7FpfkvXVWZ1ws130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56746.RAeAxa3cbCCNlzDM4LQtUxDl5sBL mjS7FpfkvXVWZ1ws130 assertion
type: Assertion
description: [Our results indicate that variants of the immunomodulatory IL10 and IL19/IL20 genes may be involved in natural clearance of HCV in the African-American population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15815689
was generated by: ECO_0000203

NP56756.RAYqa5EUY5QdQkKdNm8SDQQijFq7lT583zwgeZImg7tT8
has assertion: NP56756.RAYqa5EUY5QdQkKdNm8SDQQijFq7lT583zwgeZImg7tT8130 assertion
has provenance: NP56756.RAYqa5EUY5QdQkKdNm8SDQQijFq7lT583zwgeZImg7tT8130 provenance
has publication info: NP56756.RAYqa5EUY5QdQkKdNm8SDQQijFq7lT583zwgeZImg7tT8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56756.RAYqa5EUY5QdQkKdNm8SDQQijFq7lT583zwgeZImg7tT8130 assertion
type: Assertion
description: [In contrast, the different rates of interleukin-10 production associated with the interleukin-10 polymorphism did not affect susceptibility to tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12531774
was generated by: ECO_0000203

NP56765.RAf2IA1EHDleE3GL7-KFDBT2JiubZjl-jT362BTx8i9Mc
has assertion: NP56765.RAf2IA1EHDleE3GL7-KFDBT2JiubZjl-jT362BTx8i9Mc130 assertion
has provenance: NP56765.RAf2IA1EHDleE3GL7-KFDBT2JiubZjl-jT362BTx8i9Mc130 provenance
has publication info: NP56765.RAf2IA1EHDleE3GL7-KFDBT2JiubZjl-jT362BTx8i9Mc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56765.RAf2IA1EHDleE3GL7-KFDBT2JiubZjl-jT362BTx8i9Mc130 assertion
type: Assertion
description: [Nevertheless, these findings suggest that the TNF-alpha -308 G/G and TGF-beta codon 10-25 T/T-G/C genotypes may be potential risk factors for RCC, whereas TNF-alpha -308 G/A, IL-6 C/C and TGF-beta1 codon 10-25 C/C-G/G genotypes may be possible protective factors. The number of the cases has to be increased to investigate the independency of these polymorphisms involved in the oncogenesis of RCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15784411
was generated by: ECO_0000203

NP56771.RAStghvIE6jhKtw8v7PPIrbru1pBfrLrJPKhXZMFeoTg0
has assertion: NP56771.RAStghvIE6jhKtw8v7PPIrbru1pBfrLrJPKhXZMFeoTg0130 assertion
has provenance: NP56771.RAStghvIE6jhKtw8v7PPIrbru1pBfrLrJPKhXZMFeoTg0130 provenance
has publication info: NP56771.RAStghvIE6jhKtw8v7PPIrbru1pBfrLrJPKhXZMFeoTg0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56771.RAStghvIE6jhKtw8v7PPIrbru1pBfrLrJPKhXZMFeoTg0130 assertion
type: Assertion
description: [Interleukin 10 polymorphisms as predictors of sustained response in antiviral therapy for chronic hepatitis C infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11230752
was generated by: ECO_0000203

NP56772.RAUaEr15WPlf4Nfwr Pd8cHZ WlRferWebWKYY19ZhTLE
has assertion: NP56772.RAUaEr15WPlf4Nfwr Pd8cHZ WlRferWebWKYY19ZhTLE130 assertion
has provenance: NP56772.RAUaEr15WPlf4Nfwr Pd8cHZ WlRferWebWKYY19ZhTLE130 provenance
has publication info: NP56772.RAUaEr15WPlf4Nfwr Pd8cHZ WlRferWebWKYY19ZhTLE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56772.RAUaEr15WPlf4Nfwr Pd8cHZ WlRferWebWKYY19ZhTLE130 assertion
type: Assertion
description: [Interleukin (IL) 1beta and IL-10 gene polymorphism in chronic hepatitis C patients with normal or elevated alanine aminotransferase levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12705485
was generated by: ECO_0000203

NP56779.RAZa-kqEoBAbXcrrH0VfU0QENXj7lQ3iBQe5VGRyA7SAI
has assertion: NP56779.RAZa-kqEoBAbXcrrH0VfU0QENXj7lQ3iBQe5VGRyA7SAI130 assertion
has provenance: NP56779.RAZa-kqEoBAbXcrrH0VfU0QENXj7lQ3iBQe5VGRyA7SAI130 provenance
has publication info: NP56779.RAZa-kqEoBAbXcrrH0VfU0QENXj7lQ3iBQe5VGRyA7SAI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56779.RAZa-kqEoBAbXcrrH0VfU0QENXj7lQ3iBQe5VGRyA7SAI130 assertion
type: Assertion
description: [To analyse the role of polymorphisms of the interleukin-10 promoter region in the epidemiologic, clinical and immunologic characteristics of patients with primary Sjgren's syndrome (SS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12209037
was generated by: ECO_0000203

NP56780.RARIxb-KREDYWxLjDnU1YAlvHiKhgKnnF1jlH0a2xiCko
has assertion: NP56780.RARIxb-KREDYWxLjDnU1YAlvHiKhgKnnF1jlH0a2xiCko130 assertion
has provenance: NP56780.RARIxb-KREDYWxLjDnU1YAlvHiKhgKnnF1jlH0a2xiCko130 provenance
has publication info: NP56780.RARIxb-KREDYWxLjDnU1YAlvHiKhgKnnF1jlH0a2xiCko130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56780.RARIxb-KREDYWxLjDnU1YAlvHiKhgKnnF1jlH0a2xiCko130 assertion
type: Assertion
description: [Autoimmune response in pSS patients as well as salivary gland disease activity and cutaneous involvement appears to be mediated by IL-10 levels; in turn, there is a linkage with IL-10 gene polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12233881
was generated by: ECO_0000203

NP56782.RATkmJ96 WEQBbO1jetrMT8RU FIMv-ncuesFfkVTQTQU
has assertion: NP56782.RATkmJ96 WEQBbO1jetrMT8RU FIMv-ncuesFfkVTQTQU130 assertion
has provenance: NP56782.RATkmJ96 WEQBbO1jetrMT8RU FIMv-ncuesFfkVTQTQU130 provenance
has publication info: NP56782.RATkmJ96 WEQBbO1jetrMT8RU FIMv-ncuesFfkVTQTQU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56782.RATkmJ96 WEQBbO1jetrMT8RU FIMv-ncuesFfkVTQTQU130 assertion
type: Assertion
description: [The aim of this study was to assess the relationship between polymorphisms involving five cytokine genes (TNF-alpha, TGF-beta, IL-10, IL-6, and IFN-gamma), and IBD susceptibility and disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15842590
was generated by: ECO_0000203

NP56783.RAW8vFEpeVpc0WuzWIXbVQIRv-lJUJkXsEI19p-jup3nk
has assertion: NP56783.RAW8vFEpeVpc0WuzWIXbVQIRv-lJUJkXsEI19p-jup3nk130 assertion
has provenance: NP56783.RAW8vFEpeVpc0WuzWIXbVQIRv-lJUJkXsEI19p-jup3nk130 provenance
has publication info: NP56783.RAW8vFEpeVpc0WuzWIXbVQIRv-lJUJkXsEI19p-jup3nk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56783.RAW8vFEpeVpc0WuzWIXbVQIRv-lJUJkXsEI19p-jup3nk130 assertion
type: Assertion
description: [Interleukin 10 promoter region polymorphisms in inflammatory bowel disease in Tunisian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19184348
was generated by: ECO_0000203

NP56784.RAXRN8KY954obBi2ecogVmSwzasRWibYJ8hdo1yF2CAig
has assertion: NP56784.RAXRN8KY954obBi2ecogVmSwzasRWibYJ8hdo1yF2CAig130 assertion
has provenance: NP56784.RAXRN8KY954obBi2ecogVmSwzasRWibYJ8hdo1yF2CAig130 provenance
has publication info: NP56784.RAXRN8KY954obBi2ecogVmSwzasRWibYJ8hdo1yF2CAig130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56784.RAXRN8KY954obBi2ecogVmSwzasRWibYJ8hdo1yF2CAig130 assertion
type: Assertion
description: [ Psoriasis is not determined by a genotype consistent with high production of Th1 cytokines or low production of Th2 cytokines. Thus, the Th1 cytokine profile found in psoriatic plaques is most likely a consequence of local factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11298547
was generated by: ECO_0000203

NP56785.RAfiuVmyFRDGy5EpmTwAhfeeA7R2RECZELtN4H56tPl-c
has assertion: NP56785.RAfiuVmyFRDGy5EpmTwAhfeeA7R2RECZELtN4H56tPl-c130 assertion
has provenance: NP56785.RAfiuVmyFRDGy5EpmTwAhfeeA7R2RECZELtN4H56tPl-c130 provenance
has publication info: NP56785.RAfiuVmyFRDGy5EpmTwAhfeeA7R2RECZELtN4H56tPl-c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56785.RAfiuVmyFRDGy5EpmTwAhfeeA7R2RECZELtN4H56tPl-c130 assertion
type: Assertion
description: [Polymorphisms of N-acetyltransferase 2, glutathione S-transferases T1 and M1, and promoter polymorphisms of the genes encoding for tumor necrosis factor-alpha and interleukin-10 were investigated in 151 Caucasian patients with psoriasis (100 with type I and 51 with type II psoriasis) and in 123 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10469306
was generated by: ECO_0000203

NP56791.RAWOl7gHZfwjaHBbtQpAis18YpuBYEvC5viutH2K4dy4Y
has assertion: NP56791.RAWOl7gHZfwjaHBbtQpAis18YpuBYEvC5viutH2K4dy4Y130 assertion
has provenance: NP56791.RAWOl7gHZfwjaHBbtQpAis18YpuBYEvC5viutH2K4dy4Y130 provenance
has publication info: NP56791.RAWOl7gHZfwjaHBbtQpAis18YpuBYEvC5viutH2K4dy4Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56791.RAWOl7gHZfwjaHBbtQpAis18YpuBYEvC5viutH2K4dy4Y130 assertion
type: Assertion
description: [ These data suggest that variations in genes involved in immune regulation are associated with biologic and clinical phenotypes in the first year of life that might increase the risk for the subsequent development of childhood asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15007355
was generated by: ECO_0000203

NP56792.RAWh8VQclHEMAobPeAqXZ4EYUqL0gRk95Cb0RhXvZGMas
has assertion: NP56792.RAWh8VQclHEMAobPeAqXZ4EYUqL0gRk95Cb0RhXvZGMas130 assertion
has provenance: NP56792.RAWh8VQclHEMAobPeAqXZ4EYUqL0gRk95Cb0RhXvZGMas130 provenance
has publication info: NP56792.RAWh8VQclHEMAobPeAqXZ4EYUqL0gRk95Cb0RhXvZGMas130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56792.RAWh8VQclHEMAobPeAqXZ4EYUqL0gRk95Cb0RhXvZGMas130 assertion
type: Assertion
description: [Comprehensive characterization of genetic variation in extended cytokine candidate gene regions is now needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16759385
was generated by: ECO_0000203

NP56803.RAfde4ZbOhjWFW4pjPwhXmPetWl9uq3L6cLuhVZ7anDBU
has assertion: NP56803.RAfde4ZbOhjWFW4pjPwhXmPetWl9uq3L6cLuhVZ7anDBU130 assertion
has provenance: NP56803.RAfde4ZbOhjWFW4pjPwhXmPetWl9uq3L6cLuhVZ7anDBU130 provenance
has publication info: NP56803.RAfde4ZbOhjWFW4pjPwhXmPetWl9uq3L6cLuhVZ7anDBU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56803.RAfde4ZbOhjWFW4pjPwhXmPetWl9uq3L6cLuhVZ7anDBU130 assertion
type: Assertion
description: [Our data suggest that the FAS 1377G>A and IL10 592C>A polymorphisms could modify disease-free and overall survival in women with lymph node-positive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20204402
was generated by: ECO_0000203

NP56804.RAVpw68 6h2u6vX-AAuqeByKRt8FKo2g4lxms2w6L-lEI
has assertion: NP56804.RAVpw68 6h2u6vX-AAuqeByKRt8FKo2g4lxms2w6L-lEI130 assertion
has provenance: NP56804.RAVpw68 6h2u6vX-AAuqeByKRt8FKo2g4lxms2w6L-lEI130 provenance
has publication info: NP56804.RAVpw68 6h2u6vX-AAuqeByKRt8FKo2g4lxms2w6L-lEI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56804.RAVpw68 6h2u6vX-AAuqeByKRt8FKo2g4lxms2w6L-lEI130 assertion
type: Assertion
description: [PTGS2 and ERCC5 were associated with stomach cancer risk in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19661089
was generated by: ECO_0000203

NP56805.RAZzZQXq6jsYHW0w7l9I52di45Xa2CNl2z8nfynDmqRik
has assertion: NP56805.RAZzZQXq6jsYHW0w7l9I52di45Xa2CNl2z8nfynDmqRik130 assertion
has provenance: NP56805.RAZzZQXq6jsYHW0w7l9I52di45Xa2CNl2z8nfynDmqRik130 provenance
has publication info: NP56805.RAZzZQXq6jsYHW0w7l9I52di45Xa2CNl2z8nfynDmqRik130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56805.RAZzZQXq6jsYHW0w7l9I52di45Xa2CNl2z8nfynDmqRik130 assertion
type: Assertion
description: [The analysis of combined genotypes of the studied genes suggests a synergic action of genes Fc gamma RIIIA and IL-10 on the risk to develop SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12847896
was generated by: ECO_0000203

NP56808.RAWWn5hoiH17I5bL KfjtNKTK2fEDrWd ls51cWNamEnk
has assertion: NP56808.RAWWn5hoiH17I5bL KfjtNKTK2fEDrWd ls51cWNamEnk130 assertion
has provenance: NP56808.RAWWn5hoiH17I5bL KfjtNKTK2fEDrWd ls51cWNamEnk130 provenance
has publication info: NP56808.RAWWn5hoiH17I5bL KfjtNKTK2fEDrWd ls51cWNamEnk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56808.RAWWn5hoiH17I5bL KfjtNKTK2fEDrWd ls51cWNamEnk130 assertion
type: Assertion
description: [A significant increase was found in SLE patients (0.170 versus 0.095; chi2y = 4.11, P = 0.0425) in the frequency of the 140-basepair allele of the IL10.G microsatellite located in the promoter region of the IL-10 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10643707
was generated by: ECO_0000203

NP56811.RAdAlu6DGjLx17m SMY9yzT13ZgDNlRfPepX3o0rISdbE
has assertion: NP56811.RAdAlu6DGjLx17m SMY9yzT13ZgDNlRfPepX3o0rISdbE130 assertion
has provenance: NP56811.RAdAlu6DGjLx17m SMY9yzT13ZgDNlRfPepX3o0rISdbE130 provenance
has publication info: NP56811.RAdAlu6DGjLx17m SMY9yzT13ZgDNlRfPepX3o0rISdbE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56811.RAdAlu6DGjLx17m SMY9yzT13ZgDNlRfPepX3o0rISdbE130 assertion
type: Assertion
description: [Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16380445
was generated by: ECO_0000203

NP56814.RAQwuq6xVZblnY5MydWXrXr 3qt0mtyUHQKq3bgiQgJKc
has assertion: NP56814.RAQwuq6xVZblnY5MydWXrXr 3qt0mtyUHQKq3bgiQgJKc130 assertion
has provenance: NP56814.RAQwuq6xVZblnY5MydWXrXr 3qt0mtyUHQKq3bgiQgJKc130 provenance
has publication info: NP56814.RAQwuq6xVZblnY5MydWXrXr 3qt0mtyUHQKq3bgiQgJKc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56814.RAQwuq6xVZblnY5MydWXrXr 3qt0mtyUHQKq3bgiQgJKc130 assertion
type: Assertion
description: [In conclusion, antigenic stimulation by HER-modified CYP2E1 combined with an impaired control of T-cell proliferation by CTLA-4 mutation promotes the development of anti-CYP2E1 autoantibodies that might contribute to alcohol-induced liver injury.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12540792
was generated by: ECO_0000203

NP56815.RAQqk-DmDW5px6f m5 koiwCPRsQ1YIMwh6u54zFmr0To
has assertion: NP56815.RAQqk-DmDW5px6f m5 koiwCPRsQ1YIMwh6u54zFmr0To130 assertion
has provenance: NP56815.RAQqk-DmDW5px6f m5 koiwCPRsQ1YIMwh6u54zFmr0To130 provenance
has publication info: NP56815.RAQqk-DmDW5px6f m5 koiwCPRsQ1YIMwh6u54zFmr0To130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56815.RAQqk-DmDW5px6f m5 koiwCPRsQ1YIMwh6u54zFmr0To130 assertion
type: Assertion
description: [No association was found between the previously implicated polymorphisms of TNF-alpha, IL-10, CD14 and MnSOD, either individually or simultaneously, and the presence of established ALD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16148556
was generated by: ECO_0000203

NP56819.RAQYCmrlNXoOZ9y0L09nG4H-uMRB7WsGDfjtsva3FIU5U
has assertion: NP56819.RAQYCmrlNXoOZ9y0L09nG4H-uMRB7WsGDfjtsva3FIU5U130 assertion
has provenance: NP56819.RAQYCmrlNXoOZ9y0L09nG4H-uMRB7WsGDfjtsva3FIU5U130 provenance
has publication info: NP56819.RAQYCmrlNXoOZ9y0L09nG4H-uMRB7WsGDfjtsva3FIU5U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56819.RAQYCmrlNXoOZ9y0L09nG4H-uMRB7WsGDfjtsva3FIU5U130 assertion
type: Assertion
description: [Cytokine polymorphisms in the Th1/Th2 pathway and susceptibility to non-Hodgkin lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16449530
was generated by: ECO_0000203

NP56831.RAX-7U8SzOXEmikygjbjedC7gLPjowqrvySdS5Dnx5vbM
has assertion: NP56831.RAX-7U8SzOXEmikygjbjedC7gLPjowqrvySdS5Dnx5vbM130 assertion
has provenance: NP56831.RAX-7U8SzOXEmikygjbjedC7gLPjowqrvySdS5Dnx5vbM130 provenance
has publication info: NP56831.RAX-7U8SzOXEmikygjbjedC7gLPjowqrvySdS5Dnx5vbM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56831.RAX-7U8SzOXEmikygjbjedC7gLPjowqrvySdS5Dnx5vbM130 assertion
type: Assertion
description: [Toll-like receptor signaling pathway variants and prostate cancer mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19505919
was generated by: ECO_0000203

NP56835.RASLQ8XNki8JSwC063H864XtCngbMW-z1L2Yr3q6bqW38
has assertion: NP56835.RASLQ8XNki8JSwC063H864XtCngbMW-z1L2Yr3q6bqW38130 assertion
has provenance: NP56835.RASLQ8XNki8JSwC063H864XtCngbMW-z1L2Yr3q6bqW38130 provenance
has publication info: NP56835.RASLQ8XNki8JSwC063H864XtCngbMW-z1L2Yr3q6bqW38130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56835.RASLQ8XNki8JSwC063H864XtCngbMW-z1L2Yr3q6bqW38130 assertion
type: Assertion
description: [Interleukin 10.G microsatellite in the promoter region of the interleukin-10 gene in severe sepsis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16537004
was generated by: ECO_0000203

NP56842.RAeOA6WKFUMh6-OaD0aSytxT6nEpnx92W SyQDX84m82E
has assertion: NP56842.RAeOA6WKFUMh6-OaD0aSytxT6nEpnx92W SyQDX84m82E130 assertion
has provenance: NP56842.RAeOA6WKFUMh6-OaD0aSytxT6nEpnx92W SyQDX84m82E130 provenance
has publication info: NP56842.RAeOA6WKFUMh6-OaD0aSytxT6nEpnx92W SyQDX84m82E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56842.RAeOA6WKFUMh6-OaD0aSytxT6nEpnx92W SyQDX84m82E130 assertion
type: Assertion
description: [Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18583979
was generated by: ECO_0000203

NP56843.RARrvKWvQDuVSuZ9f0lD-Y3OHMsyhwpe7jWgWZDQaQ5vM
has assertion: NP56843.RARrvKWvQDuVSuZ9f0lD-Y3OHMsyhwpe7jWgWZDQaQ5vM130 assertion
has provenance: NP56843.RARrvKWvQDuVSuZ9f0lD-Y3OHMsyhwpe7jWgWZDQaQ5vM130 provenance
has publication info: NP56843.RARrvKWvQDuVSuZ9f0lD-Y3OHMsyhwpe7jWgWZDQaQ5vM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56843.RARrvKWvQDuVSuZ9f0lD-Y3OHMsyhwpe7jWgWZDQaQ5vM130 assertion
type: Assertion
description: [In the present study it was aimed to examine the IL-10 gene promoter region's polymorphic variants in patients with schizophrenia in a population of the Elazig Region of East Anatolia, Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19153889
was generated by: ECO_0000203

NP56847.RARqTiOjWi8lMzjYTGGrFD9w9URRmw1Z q1jTP3DxaKHE
has assertion: NP56847.RARqTiOjWi8lMzjYTGGrFD9w9URRmw1Z q1jTP3DxaKHE130 assertion
has provenance: NP56847.RARqTiOjWi8lMzjYTGGrFD9w9URRmw1Z q1jTP3DxaKHE130 provenance
has publication info: NP56847.RARqTiOjWi8lMzjYTGGrFD9w9URRmw1Z q1jTP3DxaKHE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56847.RARqTiOjWi8lMzjYTGGrFD9w9URRmw1Z q1jTP3DxaKHE130 assertion
type: Assertion
description: [ The results of this preliminary study confirm that the pro-inflammatory IL-1B genotypes, as well as male gender, are risk factors for development of gastric cancer in Mexican population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15127646
was generated by: ECO_0000203

NP56851.RAQ2Ug2H-OvHcRDjZz6o11Q4Gud OjvBJ9PvSB6FLx2QY
has assertion: NP56851.RAQ2Ug2H-OvHcRDjZz6o11Q4Gud OjvBJ9PvSB6FLx2QY130 assertion
has provenance: NP56851.RAQ2Ug2H-OvHcRDjZz6o11Q4Gud OjvBJ9PvSB6FLx2QY130 provenance
has publication info: NP56851.RAQ2Ug2H-OvHcRDjZz6o11Q4Gud OjvBJ9PvSB6FLx2QY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56851.RAQ2Ug2H-OvHcRDjZz6o11Q4Gud OjvBJ9PvSB6FLx2QY130 assertion
type: Assertion
description: [A comprehensive analysis of 207 SNP of 11 cytokine genes revealed that variations in IL-4 and IL-1RN genes are negatively associated with the risk of developing gastric cancer following H. pylori infection. Distinct host cytokine responses in the gastric mucosa might have a role in H. pylori-induced carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17444864
was generated by: ECO_0000203

NP56859.RAUn7t1LVvguYTZjK0JAEkmTFRUhq8m3kWIYgWjQ0W4jY
has assertion: NP56859.RAUn7t1LVvguYTZjK0JAEkmTFRUhq8m3kWIYgWjQ0W4jY130 assertion
has provenance: NP56859.RAUn7t1LVvguYTZjK0JAEkmTFRUhq8m3kWIYgWjQ0W4jY130 provenance
has publication info: NP56859.RAUn7t1LVvguYTZjK0JAEkmTFRUhq8m3kWIYgWjQ0W4jY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56859.RAUn7t1LVvguYTZjK0JAEkmTFRUhq8m3kWIYgWjQ0W4jY130 assertion
type: Assertion
description: [Our results suggest a contribution of the anti-inflammatory cytokines gene polymorphisms in sar- coidosis mainly in what susceptibility and clinical course is concerned. Key-wordgene polymorphisms, anti-inflammatory cytoki- nes, sarcoidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17206322
was generated by: ECO_0000203

NP56860.RAffQdPef 7vC-JbpjsYxuJvLDPIaT3ndg8IxKZH66DjQ
has assertion: NP56860.RAffQdPef 7vC-JbpjsYxuJvLDPIaT3ndg8IxKZH66DjQ130 assertion
has provenance: NP56860.RAffQdPef 7vC-JbpjsYxuJvLDPIaT3ndg8IxKZH66DjQ130 provenance
has publication info: NP56860.RAffQdPef 7vC-JbpjsYxuJvLDPIaT3ndg8IxKZH66DjQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56860.RAffQdPef 7vC-JbpjsYxuJvLDPIaT3ndg8IxKZH66DjQ130 assertion
type: Assertion
description: [The results of our study support the hypothesis of a genetically encoded immune regulation imbalance in sarcoidosis. The high-producer IL-10 (-819) and (-592) CC genotypes and intermediate- producer IL-10 (-1082) (-819) (-592) ACC haplotype 2 present in the majority of our sarcoidosis patients could support the role of genetically encoded disregulation of cell- mediated immune response to an unknown antigen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21086908
was generated by: ECO_0000203

NP56861.RAURwXjrbCGDMTVpaEaNwXp-0jbjNExjA557gj tQs6p8
has assertion: NP56861.RAURwXjrbCGDMTVpaEaNwXp-0jbjNExjA557gj tQs6p8130 assertion
has provenance: NP56861.RAURwXjrbCGDMTVpaEaNwXp-0jbjNExjA557gj tQs6p8130 provenance
has publication info: NP56861.RAURwXjrbCGDMTVpaEaNwXp-0jbjNExjA557gj tQs6p8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56861.RAURwXjrbCGDMTVpaEaNwXp-0jbjNExjA557gj tQs6p8130 assertion
type: Assertion
description: [We suggest that dysregulation of both IL-6 and IL-10 in some elderly people, due in part to genetic variations in the two genes, contributes to the development of AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19698145
was generated by: ECO_0000203

NP56863.RAVmvRQtUDks1D224vEw8LXjnzOeMqkZfP5uk6RcEnHB8
has assertion: NP56863.RAVmvRQtUDks1D224vEw8LXjnzOeMqkZfP5uk6RcEnHB8130 assertion
has provenance: NP56863.RAVmvRQtUDks1D224vEw8LXjnzOeMqkZfP5uk6RcEnHB8130 provenance
has publication info: NP56863.RAVmvRQtUDks1D224vEw8LXjnzOeMqkZfP5uk6RcEnHB8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56863.RAVmvRQtUDks1D224vEw8LXjnzOeMqkZfP5uk6RcEnHB8130 assertion
type: Assertion
description: [We have used immunohistochemistry, Western blotting, real time-PCR (RT-PCR) on frontal (BA 6/24) and temporal (BA 20-22) neocortex and hippocampus from AD and control brains as well as genetic association analysis to address the possible involvement of IL-10 in AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16973274
was generated by: ECO_0000203

NP56875.RAW0OYwQ0v6Y86skECLgdYB1SZy5RFqg0LlQRtPLVVgbQ
has assertion: NP56875.RAW0OYwQ0v6Y86skECLgdYB1SZy5RFqg0LlQRtPLVVgbQ130 assertion
has provenance: NP56875.RAW0OYwQ0v6Y86skECLgdYB1SZy5RFqg0LlQRtPLVVgbQ130 provenance
has publication info: NP56875.RAW0OYwQ0v6Y86skECLgdYB1SZy5RFqg0LlQRtPLVVgbQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56875.RAW0OYwQ0v6Y86skECLgdYB1SZy5RFqg0LlQRtPLVVgbQ130 assertion
type: Assertion
description: [Progression of periodontal disease and interleukin-10 gene polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18447856
was generated by: ECO_0000203

NP56877.RAZkkGSQ2Jrdm-kkYfrvElq UpapZtIQQCgDfhCmNYkHM
has assertion: NP56877.RAZkkGSQ2Jrdm-kkYfrvElq UpapZtIQQCgDfhCmNYkHM130 assertion
has provenance: NP56877.RAZkkGSQ2Jrdm-kkYfrvElq UpapZtIQQCgDfhCmNYkHM130 provenance
has publication info: NP56877.RAZkkGSQ2Jrdm-kkYfrvElq UpapZtIQQCgDfhCmNYkHM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56877.RAZkkGSQ2Jrdm-kkYfrvElq UpapZtIQQCgDfhCmNYkHM130 assertion
type: Assertion
description: [Interleukin-10 gene promoter polymorphism in Japanese patients with adult and early-onset periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11493351
was generated by: ECO_0000203

NP56884.RAVgFpMnowmw7R5nZEBrOrkYzpcP7JFbLyx9a76sPGmaY
has assertion: NP56884.RAVgFpMnowmw7R5nZEBrOrkYzpcP7JFbLyx9a76sPGmaY130 assertion
has provenance: NP56884.RAVgFpMnowmw7R5nZEBrOrkYzpcP7JFbLyx9a76sPGmaY130 provenance
has publication info: NP56884.RAVgFpMnowmw7R5nZEBrOrkYzpcP7JFbLyx9a76sPGmaY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56884.RAVgFpMnowmw7R5nZEBrOrkYzpcP7JFbLyx9a76sPGmaY130 assertion
type: Assertion
description: [Susceptibility to primary Epstein-Barr virus infection is associated with interleukin-10 gene promoter polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11517440
was generated by: ECO_0000203

NP56885.RAfRGeIq0p3Rf4fwkoS9NSh39CuLcTdXnnqif6d78ZhbI
has assertion: NP56885.RAfRGeIq0p3Rf4fwkoS9NSh39CuLcTdXnnqif6d78ZhbI130 assertion
has provenance: NP56885.RAfRGeIq0p3Rf4fwkoS9NSh39CuLcTdXnnqif6d78ZhbI130 provenance
has publication info: NP56885.RAfRGeIq0p3Rf4fwkoS9NSh39CuLcTdXnnqif6d78ZhbI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56885.RAfRGeIq0p3Rf4fwkoS9NSh39CuLcTdXnnqif6d78ZhbI130 assertion
type: Assertion
description: [Novel genetic association of Wegener's granulomatosis with the interleukin 10 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11838849
was generated by: ECO_0000203

NP56886.RAaXwtTWtZ581ftH2C5kUm42TVwgab88eI22I6dGy1LcQ
has assertion: NP56886.RAaXwtTWtZ581ftH2C5kUm42TVwgab88eI22I6dGy1LcQ130 assertion
has provenance: NP56886.RAaXwtTWtZ581ftH2C5kUm42TVwgab88eI22I6dGy1LcQ130 provenance
has publication info: NP56886.RAaXwtTWtZ581ftH2C5kUm42TVwgab88eI22I6dGy1LcQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56886.RAaXwtTWtZ581ftH2C5kUm42TVwgab88eI22I6dGy1LcQ130 assertion
type: Assertion
description: [The most interesting result was the observed, significant shift to genotype AA of the IL-10 polymorphism in Wegener's granulomatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11715070
was generated by: ECO_0000203

NP56887.RAeRd8-KXpz268JNyA3zL3fcQ I2AZNTA67TcIqJalmcc
has assertion: NP56887.RAeRd8-KXpz268JNyA3zL3fcQ I2AZNTA67TcIqJalmcc130 assertion
has provenance: NP56887.RAeRd8-KXpz268JNyA3zL3fcQ I2AZNTA67TcIqJalmcc130 provenance
has publication info: NP56887.RAeRd8-KXpz268JNyA3zL3fcQ I2AZNTA67TcIqJalmcc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56887.RAeRd8-KXpz268JNyA3zL3fcQ I2AZNTA67TcIqJalmcc130 assertion
type: Assertion
description: [Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5' regulatory region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12486603
was generated by: ECO_0000203

NP56894.RAc-IRthHGI UQQmyhHADYftmLHD42RiMa8moxWT70EOA
has assertion: NP56894.RAc-IRthHGI UQQmyhHADYftmLHD42RiMa8moxWT70EOA130 assertion
has provenance: NP56894.RAc-IRthHGI UQQmyhHADYftmLHD42RiMa8moxWT70EOA130 provenance
has publication info: NP56894.RAc-IRthHGI UQQmyhHADYftmLHD42RiMa8moxWT70EOA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56894.RAc-IRthHGI UQQmyhHADYftmLHD42RiMa8moxWT70EOA130 assertion
type: Assertion
description: [We analyzed 11 functional polymorphisms in tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-1, IL-4 and IL-10 genes in 220 Taiwanese Chinese with GC and in 230 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12594817
was generated by: ECO_0000203

NP56895.RAYqCr5hg5RaSEtdhbw142Z5jSv8RKggo8x8YSfWcQ7t8
has assertion: NP56895.RAYqCr5hg5RaSEtdhbw142Z5jSv8RKggo8x8YSfWcQ7t8130 assertion
has provenance: NP56895.RAYqCr5hg5RaSEtdhbw142Z5jSv8RKggo8x8YSfWcQ7t8130 provenance
has publication info: NP56895.RAYqCr5hg5RaSEtdhbw142Z5jSv8RKggo8x8YSfWcQ7t8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56895.RAYqCr5hg5RaSEtdhbw142Z5jSv8RKggo8x8YSfWcQ7t8130 assertion
type: Assertion
description: [We believe that the associations of these genotypes with RPL are interesting not only as risk factors but also because they represent another piece of evidence that these cytokines might be important in the pathogenesis of RPL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12609526
was generated by: ECO_0000203

NP56903.RAcnTi0ToVkHmDCFIyHzro7U184SVzmIAWm-hOeQOw PQ
has assertion: NP56903.RAcnTi0ToVkHmDCFIyHzro7U184SVzmIAWm-hOeQOw PQ130 assertion
has provenance: NP56903.RAcnTi0ToVkHmDCFIyHzro7U184SVzmIAWm-hOeQOw PQ130 provenance
has publication info: NP56903.RAcnTi0ToVkHmDCFIyHzro7U184SVzmIAWm-hOeQOw PQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56903.RAcnTi0ToVkHmDCFIyHzro7U184SVzmIAWm-hOeQOw PQ130 assertion
type: Assertion
description: [Further studies of variation in the IL10 gene may help elucidate the mechanism of asthma development in children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14748015
was generated by: ECO_0000203

NP56904.RAQrHPJZlDConZCkPO-wleNSDhfST1Cf-X8RT3sfHYA88
has assertion: NP56904.RAQrHPJZlDConZCkPO-wleNSDhfST1Cf-X8RT3sfHYA88130 assertion
has provenance: NP56904.RAQrHPJZlDConZCkPO-wleNSDhfST1Cf-X8RT3sfHYA88130 provenance
has publication info: NP56904.RAQrHPJZlDConZCkPO-wleNSDhfST1Cf-X8RT3sfHYA88130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56904.RAQrHPJZlDConZCkPO-wleNSDhfST1Cf-X8RT3sfHYA88130 assertion
type: Assertion
description: [Interleukin-10 promoter polymorphisms and atopic asthma in North Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16008678
was generated by: ECO_0000203

NP56917.RAX-Km8-aqCyvGXLu0jHU1WKBY1bHmOKUI90fyFvo6yQc
has assertion: NP56917.RAX-Km8-aqCyvGXLu0jHU1WKBY1bHmOKUI90fyFvo6yQc130 assertion
has provenance: NP56917.RAX-Km8-aqCyvGXLu0jHU1WKBY1bHmOKUI90fyFvo6yQc130 provenance
has publication info: NP56917.RAX-Km8-aqCyvGXLu0jHU1WKBY1bHmOKUI90fyFvo6yQc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56917.RAX-Km8-aqCyvGXLu0jHU1WKBY1bHmOKUI90fyFvo6yQc130 assertion
type: Assertion
description: [ Ig KM and GM genes do not contribute to susceptibility to pSS. The Ig KM1 allele is associated with several markers of immunologically active disease, whereas the Ig GM z allele is associated with milder pSS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15517630
was generated by: ECO_0000203

NP56921.RAVdtNl0jLJydEN-MihHxe5M9QPtiIQiRCDHAmOg9w75o
has assertion: NP56921.RAVdtNl0jLJydEN-MihHxe5M9QPtiIQiRCDHAmOg9w75o130 assertion
has provenance: NP56921.RAVdtNl0jLJydEN-MihHxe5M9QPtiIQiRCDHAmOg9w75o130 provenance
has publication info: NP56921.RAVdtNl0jLJydEN-MihHxe5M9QPtiIQiRCDHAmOg9w75o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56921.RAVdtNl0jLJydEN-MihHxe5M9QPtiIQiRCDHAmOg9w75o130 assertion
type: Assertion
description: [In conclusion, the IGFBP-3 -202 A/C polymorphism was not associated with susceptibility to PCa and BPH in Japanese men, but the presence of the C allele may cumulatively increase the risk for tumor metastasis and for having tumors with a biologically more aggressive phenotype. Because of the significant differences in incidence of clinically evident PCa according to racial backgrounds, the conjecture should be further examined in different racial populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12907612
was generated by: ECO_0000203

NP56930.RATSDSLsE8DVICZY69sxgsbJNWbc26-qBfB0ciLxf6F00
has assertion: NP56930.RATSDSLsE8DVICZY69sxgsbJNWbc26-qBfB0ciLxf6F00130 assertion
has provenance: NP56930.RATSDSLsE8DVICZY69sxgsbJNWbc26-qBfB0ciLxf6F00130 provenance
has publication info: NP56930.RATSDSLsE8DVICZY69sxgsbJNWbc26-qBfB0ciLxf6F00130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56930.RATSDSLsE8DVICZY69sxgsbJNWbc26-qBfB0ciLxf6F00130 assertion
type: Assertion
description: [ Both IRS1 and IRS2 variants were associated with colon cancer risk independently. Associations were slightly stronger when polymorphisms in multiple genes were evaluated in conjunction with other genes rather than individually. These data suggest that the insulin-related pathway may be important in the etiology of colon cancer but not rectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15247132
was generated by: ECO_0000203

NP56941.RAYjs1nJB5AjDtN8RUqvLXfQ022jZzFYfnkve1h--OfJA
has assertion: NP56941.RAYjs1nJB5AjDtN8RUqvLXfQ022jZzFYfnkve1h--OfJA130 assertion
has provenance: NP56941.RAYjs1nJB5AjDtN8RUqvLXfQ022jZzFYfnkve1h--OfJA130 provenance
has publication info: NP56941.RAYjs1nJB5AjDtN8RUqvLXfQ022jZzFYfnkve1h--OfJA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56941.RAYjs1nJB5AjDtN8RUqvLXfQ022jZzFYfnkve1h--OfJA130 assertion
type: Assertion
description: [Pooling data within a large consortium has helped to clarify associations of SNPs with breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17018785
was generated by: ECO_0000203

NP56944.RARA BMJs2TIkz2Lg G--TpyBnA KltRADae4-EwL2QNg
has assertion: NP56944.RARA BMJs2TIkz2Lg G--TpyBnA KltRADae4-EwL2QNg130 assertion
has provenance: NP56944.RARA BMJs2TIkz2Lg G--TpyBnA KltRADae4-EwL2QNg130 provenance
has publication info: NP56944.RARA BMJs2TIkz2Lg G--TpyBnA KltRADae4-EwL2QNg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56944.RARA BMJs2TIkz2Lg G--TpyBnA KltRADae4-EwL2QNg130 assertion
type: Assertion
description: [IGFBP3 A-202C polymorphism and breast cancer susceptibility: a meta-analysis involving 33,557 cases and 45,254 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20084546
was generated by: ECO_0000203

NP56950.RAVv5H18Xf2u-Vkn 4CIo8- wLvGvNHQS9XPkKTP3Qg9I
has assertion: NP56950.RAVv5H18Xf2u-Vkn 4CIo8- wLvGvNHQS9XPkKTP3Qg9I130 assertion
has provenance: NP56950.RAVv5H18Xf2u-Vkn 4CIo8- wLvGvNHQS9XPkKTP3Qg9I130 provenance
has publication info: NP56950.RAVv5H18Xf2u-Vkn 4CIo8- wLvGvNHQS9XPkKTP3Qg9I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56950.RAVv5H18Xf2u-Vkn 4CIo8- wLvGvNHQS9XPkKTP3Qg9I130 assertion
type: Assertion
description: [Subjects carrying the heterozygous 167-bp IGF2R genotype had a 2.7-fold higher risk of oral cancer compared with subjects with other genotypes (odds ratio = 2.7, 95% confidence interval: 1.16-6.48), controlling for major confounders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12543777
was generated by: ECO_0000203

NP56956.RAR3FntxSroRlgoHr7pFksa2oNfrHKWFf1LqQ6MN5eXag
has assertion: NP56956.RAR3FntxSroRlgoHr7pFksa2oNfrHKWFf1LqQ6MN5eXag130 assertion
has provenance: NP56956.RAR3FntxSroRlgoHr7pFksa2oNfrHKWFf1LqQ6MN5eXag130 provenance
has publication info: NP56956.RAR3FntxSroRlgoHr7pFksa2oNfrHKWFf1LqQ6MN5eXag130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56956.RAR3FntxSroRlgoHr7pFksa2oNfrHKWFf1LqQ6MN5eXag130 assertion
type: Assertion
description: [Further studies are needed to explore contributions from other genetic factors such as rare variants in these genes and variation outside of these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20810604
was generated by: ECO_0000203

NP56962.RAXhCG gM1KxVjQkweee2GWEGNiGiGuxuk1 yvqnJtjEQ
has assertion: NP56962.RAXhCG gM1KxVjQkweee2GWEGNiGiGuxuk1 yvqnJtjEQ130 assertion
has provenance: NP56962.RAXhCG gM1KxVjQkweee2GWEGNiGiGuxuk1 yvqnJtjEQ130 provenance
has publication info: NP56962.RAXhCG gM1KxVjQkweee2GWEGNiGiGuxuk1 yvqnJtjEQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56962.RAXhCG gM1KxVjQkweee2GWEGNiGiGuxuk1 yvqnJtjEQ130 assertion
type: Assertion
description: [Using resources from the Flint Men's Health Study, a population-based case control study of African-American men aged 40-79, we evaluated the associations between selected single-nucleotide polymorphisms (SNPs) in the CYP17, CYP3A4, CYP19A1, SDR5A2, IGF1, and IGFBP3 genes and prostate cancer diagnosis in 473 men (131 prostate cancer cases and 342 disease-free controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18163429
was generated by: ECO_0000203

NP56963.RAeHs0uBM4GZxSGVwp9us7pOaqO-PBcLqXpKwYITvUsD8
has assertion: NP56963.RAeHs0uBM4GZxSGVwp9us7pOaqO-PBcLqXpKwYITvUsD8130 assertion
has provenance: NP56963.RAeHs0uBM4GZxSGVwp9us7pOaqO-PBcLqXpKwYITvUsD8130 provenance
has publication info: NP56963.RAeHs0uBM4GZxSGVwp9us7pOaqO-PBcLqXpKwYITvUsD8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56963.RAeHs0uBM4GZxSGVwp9us7pOaqO-PBcLqXpKwYITvUsD8130 assertion
type: Assertion
description: [We analyzed haplotypes and three haplotype-tagging single nucleotide polymorphisms (htSNPs) in the 3' region of the IGF-I gene in relation to circulating levels IGF-I in 698 control subjects from the CAncer Prostate in Sweden (CAPS) study and 575 cases and controls from the prospective Northern Sweden Health and Disease Cohort (NSHDC) study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17911177
was generated by: ECO_0000203

NP56969.RAavsyZyb8ixNj-1w5cokKZKr0-3WeW8z31bKIeGzpft4
has assertion: NP56969.RAavsyZyb8ixNj-1w5cokKZKr0-3WeW8z31bKIeGzpft4130 assertion
has provenance: NP56969.RAavsyZyb8ixNj-1w5cokKZKr0-3WeW8z31bKIeGzpft4130 provenance
has publication info: NP56969.RAavsyZyb8ixNj-1w5cokKZKr0-3WeW8z31bKIeGzpft4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56969.RAavsyZyb8ixNj-1w5cokKZKr0-3WeW8z31bKIeGzpft4130 assertion
type: Assertion
description: [A genetic association study was performed to investigate whether radiographical osteoarthritis (ROA) was associated with specific genotypes of the insulin-like growth factor I (IGF-1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9771213
was generated by: ECO_0000203

NP56970.RAeDnbZ2OSq2mZ-0ThJ11YOCqJEihWdHG HRd4B86i-5E
has assertion: NP56970.RAeDnbZ2OSq2mZ-0ThJ11YOCqJEihWdHG HRd4B86i-5E130 assertion
has provenance: NP56970.RAeDnbZ2OSq2mZ-0ThJ11YOCqJEihWdHG HRd4B86i-5E130 provenance
has publication info: NP56970.RAeDnbZ2OSq2mZ-0ThJ11YOCqJEihWdHG HRd4B86i-5E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56970.RAeDnbZ2OSq2mZ-0ThJ11YOCqJEihWdHG HRd4B86i-5E130 assertion
type: Assertion
description: [Lack of replication is common and could be due to differences in study design, phenotype, populations examined or the occurrence of false positives in the initial study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19036616
was generated by: ECO_0000203

NP56971.RAUM5ko7FKV3-m2Y7sV6LthkVl5WGxKTe4TB8fwX0Tn68
has assertion: NP56971.RAUM5ko7FKV3-m2Y7sV6LthkVl5WGxKTe4TB8fwX0Tn68130 assertion
has provenance: NP56971.RAUM5ko7FKV3-m2Y7sV6LthkVl5WGxKTe4TB8fwX0Tn68130 provenance
has publication info: NP56971.RAUM5ko7FKV3-m2Y7sV6LthkVl5WGxKTe4TB8fwX0Tn68130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56971.RAUM5ko7FKV3-m2Y7sV6LthkVl5WGxKTe4TB8fwX0Tn68130 assertion
type: Assertion
description: [In conclusion, these studies show an association between IGF-I markers and birth size alone, symmetrical SGA, low birth weight-only SGA, and short SGA phenotypes. This suggests that IFG-I genetic variation influences growth and metabolism in fetal and postnatal life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12511011
was generated by: ECO_0000203

NP56974.RAcKVD79Q9whvZTdVGPNHasDO9r83Q2hUspxDm9Uzlcg4
has assertion: NP56974.RAcKVD79Q9whvZTdVGPNHasDO9r83Q2hUspxDm9Uzlcg4130 assertion
has provenance: NP56974.RAcKVD79Q9whvZTdVGPNHasDO9r83Q2hUspxDm9Uzlcg4130 provenance
has publication info: NP56974.RAcKVD79Q9whvZTdVGPNHasDO9r83Q2hUspxDm9Uzlcg4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56974.RAcKVD79Q9whvZTdVGPNHasDO9r83Q2hUspxDm9Uzlcg4130 assertion
type: Assertion
description: [We wanted to study if these polymorphisms or any haplotypes of the IGF1 and the IGFBP3 genes are associated with CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18031946
was generated by: ECO_0000203

NP56975.RAcuPRXbhLOQqqspVDtQs92pniACuUmbCh5zC9itrwt5Q
has assertion: NP56975.RAcuPRXbhLOQqqspVDtQs92pniACuUmbCh5zC9itrwt5Q130 assertion
has provenance: NP56975.RAcuPRXbhLOQqqspVDtQs92pniACuUmbCh5zC9itrwt5Q130 provenance
has publication info: NP56975.RAcuPRXbhLOQqqspVDtQs92pniACuUmbCh5zC9itrwt5Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56975.RAcuPRXbhLOQqqspVDtQs92pniACuUmbCh5zC9itrwt5Q130 assertion
type: Assertion
description: [Insulin-like growth factor-I (IGF-I) is involved in colorectal carcinogenesis, and elevated plasma IGF-I levels are associated with sporadic colorectal cancer (CRC) risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16418517
was generated by: ECO_0000203

NP56979.RAaYEgQQSYI5nnqNfTShhTlmxqKecx41bjNASVEgU uGY
has assertion: NP56979.RAaYEgQQSYI5nnqNfTShhTlmxqKecx41bjNASVEgU uGY130 assertion
has provenance: NP56979.RAaYEgQQSYI5nnqNfTShhTlmxqKecx41bjNASVEgU uGY130 provenance
has publication info: NP56979.RAaYEgQQSYI5nnqNfTShhTlmxqKecx41bjNASVEgU uGY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56979.RAaYEgQQSYI5nnqNfTShhTlmxqKecx41bjNASVEgU uGY130 assertion
type: Assertion
description: [Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18992148
was generated by: ECO_0000203

NP56980.RAbN bLnV3FTrUGsS9eEbSi 2FxkpgtIU1afJjyHBRlgw
has assertion: NP56980.RAbN bLnV3FTrUGsS9eEbSi 2FxkpgtIU1afJjyHBRlgw130 assertion
has provenance: NP56980.RAbN bLnV3FTrUGsS9eEbSi 2FxkpgtIU1afJjyHBRlgw130 provenance
has publication info: NP56980.RAbN bLnV3FTrUGsS9eEbSi 2FxkpgtIU1afJjyHBRlgw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56980.RAbN bLnV3FTrUGsS9eEbSi 2FxkpgtIU1afJjyHBRlgw130 assertion
type: Assertion
description: [the IGF1 CA repeat is an important modifier of disease onset in HNPCC and the first polymorphism to yield consistent results across different populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18623088
was generated by: ECO_0000203

NP56984.RAeyabwMYg6LQEt1it2Zvo6IMf9ZDEN3MSrxqG4zEIuDA
has assertion: NP56984.RAeyabwMYg6LQEt1it2Zvo6IMf9ZDEN3MSrxqG4zEIuDA130 assertion
has provenance: NP56984.RAeyabwMYg6LQEt1it2Zvo6IMf9ZDEN3MSrxqG4zEIuDA130 provenance
has publication info: NP56984.RAeyabwMYg6LQEt1it2Zvo6IMf9ZDEN3MSrxqG4zEIuDA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56984.RAeyabwMYg6LQEt1it2Zvo6IMf9ZDEN3MSrxqG4zEIuDA130 assertion
type: Assertion
description: [Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: linkage of candidate genes using two sib-pair based variance components analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18828733
was generated by: ECO_0000203

NP56995.RAQOUNGUT4m6Q6nPMr2JyImVBY4Ew0a yAquV330Y4NFA
has assertion: NP56995.RAQOUNGUT4m6Q6nPMr2JyImVBY4Ew0a yAquV330Y4NFA130 assertion
has provenance: NP56995.RAQOUNGUT4m6Q6nPMr2JyImVBY4Ew0a yAquV330Y4NFA130 provenance
has publication info: NP56995.RAQOUNGUT4m6Q6nPMr2JyImVBY4Ew0a yAquV330Y4NFA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP56995.RAQOUNGUT4m6Q6nPMr2JyImVBY4Ew0a yAquV330Y4NFA130 assertion
type: Assertion
description: [Interferon-gamma and interferon-gamma receptor 1 and 2 gene polymorphisms and restenosis following coronary stenting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16115485
was generated by: ECO_0000203

NP57001.RAb8ptGu7 kssUPRzYr1kfXCQ-ayiY3wpiYiq4QZU6p 0
has assertion: NP57001.RAb8ptGu7 kssUPRzYr1kfXCQ-ayiY3wpiYiq4QZU6p 0130 assertion
has provenance: NP57001.RAb8ptGu7 kssUPRzYr1kfXCQ-ayiY3wpiYiq4QZU6p 0130 provenance
has publication info: NP57001.RAb8ptGu7 kssUPRzYr1kfXCQ-ayiY3wpiYiq4QZU6p 0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57001.RAb8ptGu7 kssUPRzYr1kfXCQ-ayiY3wpiYiq4QZU6p 0130 assertion
type: Assertion
description: [ The IFN-GammaR2 Arg64/Arg64 genotype does not determine susceptibility to SLE in Chinese people, and the combination of IFN-Gamma R2 Arg64/Arg64 genotype and IFN-Gamma R1 Val14/Val14 genotype does not, either.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15952126
was generated by: ECO_0000203

NP57005.RAar-K4JyUOl-P5V5yBkeZuqAxWDDH6TN0scNfS0zy0jk
has assertion: NP57005.RAar-K4JyUOl-P5V5yBkeZuqAxWDDH6TN0scNfS0zy0jk130 assertion
has provenance: NP57005.RAar-K4JyUOl-P5V5yBkeZuqAxWDDH6TN0scNfS0zy0jk130 provenance
has publication info: NP57005.RAar-K4JyUOl-P5V5yBkeZuqAxWDDH6TN0scNfS0zy0jk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57005.RAar-K4JyUOl-P5V5yBkeZuqAxWDDH6TN0scNfS0zy0jk130 assertion
type: Assertion
description: [The combination of polymorphisms within interferon-gamma receptor 1 and receptor 2 associated with the risk of systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10403400
was generated by: ECO_0000203

NP57006.RAe2hlwWblr 49MrTLrU3yTHkszrl3LRJr1RvHwWYCh6k
has assertion: NP57006.RAe2hlwWblr 49MrTLrU3yTHkszrl3LRJr1RvHwWYCh6k130 assertion
has provenance: NP57006.RAe2hlwWblr 49MrTLrU3yTHkszrl3LRJr1RvHwWYCh6k130 provenance
has publication info: NP57006.RAe2hlwWblr 49MrTLrU3yTHkszrl3LRJr1RvHwWYCh6k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57006.RAe2hlwWblr 49MrTLrU3yTHkszrl3LRJr1RvHwWYCh6k130 assertion
type: Assertion
description: [Association of the interferon-gamma receptor variant (Val14Met) with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10079289
was generated by: ECO_0000203

NP57011.RAVph4UWGakMC1QBwANX7m1NPwAv30kSOv2SyhJWegA5U
has assertion: NP57011.RAVph4UWGakMC1QBwANX7m1NPwAv30kSOv2SyhJWegA5U130 assertion
has provenance: NP57011.RAVph4UWGakMC1QBwANX7m1NPwAv30kSOv2SyhJWegA5U130 provenance
has publication info: NP57011.RAVph4UWGakMC1QBwANX7m1NPwAv30kSOv2SyhJWegA5U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57011.RAVph4UWGakMC1QBwANX7m1NPwAv30kSOv2SyhJWegA5U130 assertion
type: Assertion
description: [Genetic approaches to the investigation of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11981324
was generated by: ECO_0000203

NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8 fy ClNjzqS81h8
has assertion: NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8 fy ClNjzqS81h8130 assertion
has provenance: NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8 fy ClNjzqS81h8130 provenance
has publication info: NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8 fy ClNjzqS81h8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8 fy ClNjzqS81h8130 assertion
type: Assertion
description: [ Our results demonstrate that common polymorphisms in the IFNgamma/IL-26 gene region may contribute to sex bias in susceptibility to RA, by distorting the propensity of female carriers versus male carriers to contract this disease. These results conform to our recent observations of a role for this gene cluster in sex-based differential susceptibility to another Th1-type inflammatory disease, multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14558082
was generated by: ECO_0000203

NP57015.RAZVMnzlIDsk-vmgF55F-7LCn9JUcAaHi6-43bcV tTUE
has assertion: NP57015.RAZVMnzlIDsk-vmgF55F-7LCn9JUcAaHi6-43bcV tTUE130 assertion
has provenance: NP57015.RAZVMnzlIDsk-vmgF55F-7LCn9JUcAaHi6-43bcV tTUE130 provenance
has publication info: NP57015.RAZVMnzlIDsk-vmgF55F-7LCn9JUcAaHi6-43bcV tTUE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57015.RAZVMnzlIDsk-vmgF55F-7LCn9JUcAaHi6-43bcV tTUE130 assertion
type: Assertion
description: [Association between dinucleotide repeat in non-coding region of interferon-gamma gene and susceptibility to, and severity of, rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11022930
was generated by: ECO_0000203

NP57018.RAeWqr9UbJ7 i FjwFrrxJa l-JmucqX5-sayRrHnd0E
has assertion: NP57018.RAeWqr9UbJ7 i FjwFrrxJa l-JmucqX5-sayRrHnd0E130 assertion
has provenance: NP57018.RAeWqr9UbJ7 i FjwFrrxJa l-JmucqX5-sayRrHnd0E130 provenance
has publication info: NP57018.RAeWqr9UbJ7 i FjwFrrxJa l-JmucqX5-sayRrHnd0E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57018.RAeWqr9UbJ7 i FjwFrrxJa l-JmucqX5-sayRrHnd0E130 assertion
type: Assertion
description: [IFN- gamma 3/3 was found to be associated with an increased risk of chronic graft-versus-host disease (GvHD) (11/27 vs 26/133, p=0.02). Forward logistic regression analysis confirmed the role of IFN-gamma 3/3 genotype as one of the risk factors for manifestation of chronic GvHD (OR=3.180, p=0.018) together with previous acute GvHD (OR=2.752, p=0.024), cyclosporine A monotherapy (OR=2.607, p=0.029) and malignant disorders (OR=4.371, p=0.032).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15749687
was generated by: ECO_0000203

NP57026.RAadVLLW1mmXz9ipAkg9Ek-fXyC1 pSeVlfVIn0abr2tE
has assertion: NP57026.RAadVLLW1mmXz9ipAkg9Ek-fXyC1 pSeVlfVIn0abr2tE130 assertion
has provenance: NP57026.RAadVLLW1mmXz9ipAkg9Ek-fXyC1 pSeVlfVIn0abr2tE130 provenance
has publication info: NP57026.RAadVLLW1mmXz9ipAkg9Ek-fXyC1 pSeVlfVIn0abr2tE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57026.RAadVLLW1mmXz9ipAkg9Ek-fXyC1 pSeVlfVIn0abr2tE130 assertion
type: Assertion
description: [Combined association between IFN-gamma 3,3 homozygosity and DRB1*03 in Lfgren's syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15019280
was generated by: ECO_0000203

NP57027.RAX0FI-TuCobRRDkGf d0ad-0FMe9KaMjWXP-on-seT4c
has assertion: NP57027.RAX0FI-TuCobRRDkGf d0ad-0FMe9KaMjWXP-on-seT4c130 assertion
has provenance: NP57027.RAX0FI-TuCobRRDkGf d0ad-0FMe9KaMjWXP-on-seT4c130 provenance
has publication info: NP57027.RAX0FI-TuCobRRDkGf d0ad-0FMe9KaMjWXP-on-seT4c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57027.RAX0FI-TuCobRRDkGf d0ad-0FMe9KaMjWXP-on-seT4c130 assertion
type: Assertion
description: [The results of our study support the hypothesis of a genetically encoded immune regulation imbalance in sarcoidosis. The high-producer IL-10 (-819) and (-592) CC genotypes and intermediate- producer IL-10 (-1082) (-819) (-592) ACC haplotype 2 present in the majority of our sarcoidosis patients could support the role of genetically encoded disregulation of cell- mediated immune response to an unknown antigen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21086908
was generated by: ECO_0000203

NP57028.RAVAI6CAmloTEZcJMIeLdicGZvLtrvf5HSt8E-xtTrpoc
has assertion: NP57028.RAVAI6CAmloTEZcJMIeLdicGZvLtrvf5HSt8E-xtTrpoc130 assertion
has provenance: NP57028.RAVAI6CAmloTEZcJMIeLdicGZvLtrvf5HSt8E-xtTrpoc130 provenance
has publication info: NP57028.RAVAI6CAmloTEZcJMIeLdicGZvLtrvf5HSt8E-xtTrpoc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57028.RAVAI6CAmloTEZcJMIeLdicGZvLtrvf5HSt8E-xtTrpoc130 assertion
type: Assertion
description: [ Our results suggest an association with IL-4 gene polymorphism that is dependent on HLA-DRB1 genotype in GCA susceptible individuals. These data indicate an interaction between HLA-DRB1 and IL-4 that contributes to pronounced disease susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15570643
was generated by: ECO_0000203

NP57029.RAfzIEUCwYDjeWkbeXReJTRw4obZRWUum90xyLgeULJp4
has assertion: NP57029.RAfzIEUCwYDjeWkbeXReJTRw4obZRWUum90xyLgeULJp4130 assertion
has provenance: NP57029.RAfzIEUCwYDjeWkbeXReJTRw4obZRWUum90xyLgeULJp4130 provenance
has publication info: NP57029.RAfzIEUCwYDjeWkbeXReJTRw4obZRWUum90xyLgeULJp4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57029.RAfzIEUCwYDjeWkbeXReJTRw4obZRWUum90xyLgeULJp4130 assertion
type: Assertion
description: [In conclusion, no significant association was observed between the +874 T/A polymorphism found in the first exon of the IFN-gamma gene and TB susceptibility in Turkish children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20055726
was generated by: ECO_0000203

NP57031.RAY7jyXmH4clTx4GAfPpGO51pCHFIMeqannQ5F6t2Sqhc
has assertion: NP57031.RAY7jyXmH4clTx4GAfPpGO51pCHFIMeqannQ5F6t2Sqhc130 assertion
has provenance: NP57031.RAY7jyXmH4clTx4GAfPpGO51pCHFIMeqannQ5F6t2Sqhc130 provenance
has publication info: NP57031.RAY7jyXmH4clTx4GAfPpGO51pCHFIMeqannQ5F6t2Sqhc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57031.RAY7jyXmH4clTx4GAfPpGO51pCHFIMeqannQ5F6t2Sqhc130 assertion
type: Assertion
description: [Interferon-gamma is the most important cytokine in resistance to mycobacterial diseases and common variants of interferon-gamma gene could be related to tuberculosis susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17276141
was generated by: ECO_0000203

NP57037.RAXD cHHmRn-MiKcm1WhatPJ6uRe1Y6RjmHwHC4COEfYM
has assertion: NP57037.RAXD cHHmRn-MiKcm1WhatPJ6uRe1Y6RjmHwHC4COEfYM130 assertion
has provenance: NP57037.RAXD cHHmRn-MiKcm1WhatPJ6uRe1Y6RjmHwHC4COEfYM130 provenance
has publication info: NP57037.RAXD cHHmRn-MiKcm1WhatPJ6uRe1Y6RjmHwHC4COEfYM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57037.RAXD cHHmRn-MiKcm1WhatPJ6uRe1Y6RjmHwHC4COEfYM130 assertion
type: Assertion
description: [Association of SLC11A1 with tuberculosis and interactions with NOS2A and TLR2 in African-Americans and Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19723394
was generated by: ECO_0000203

NP57041.RAd xCxF11er88 DLE3fNg0bRB8IavUS955U1wXEKY7CA
has assertion: NP57041.RAd xCxF11er88 DLE3fNg0bRB8IavUS955U1wXEKY7CA130 assertion
has provenance: NP57041.RAd xCxF11er88 DLE3fNg0bRB8IavUS955U1wXEKY7CA130 provenance
has publication info: NP57041.RAd xCxF11er88 DLE3fNg0bRB8IavUS955U1wXEKY7CA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57041.RAd xCxF11er88 DLE3fNg0bRB8IavUS955U1wXEKY7CA130 assertion
type: Assertion
description: [Genotypes of SNPs of pro-inflammatory cytokines, tumour necrosis factor-alpha -308G -->A, interleukin-6 (IL-6) -174G -->C and interferon-gamma +874G -->A, and anti-inflammatory, immunosuppressive cytokines, interleukin-10 -1082G -->A, -819C -->T and -592A -->C and transforming growth factor-beta1 (TGF-beta1) codon 10T -->C and codon 25G -->C, were determined for patients with JRA who previously participated in a long-term outcome study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15901906
was generated by: ECO_0000203

NP57044.RAVmuFCRK8rRFdPBAYSj5DbSwuPoso-53KgauH9-JXknA
has assertion: NP57044.RAVmuFCRK8rRFdPBAYSj5DbSwuPoso-53KgauH9-JXknA130 assertion
has provenance: NP57044.RAVmuFCRK8rRFdPBAYSj5DbSwuPoso-53KgauH9-JXknA130 provenance
has publication info: NP57044.RAVmuFCRK8rRFdPBAYSj5DbSwuPoso-53KgauH9-JXknA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57044.RAVmuFCRK8rRFdPBAYSj5DbSwuPoso-53KgauH9-JXknA130 assertion
type: Assertion
description: [ To our knowledge, this study is the first to demonstrate the possibility that the IL-4 promoter gene -589 T gene polymorphism with increased IL-4 synthesis in combination with IRF-1 allele 1 confers host genetic susceptibility to SSPE in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12020266
was generated by: ECO_0000203

NP57045.RAU6HnaJTk9lrRbEK-XinrLpsHa6PNHlOoGRTiEC9fmAg
has assertion: NP57045.RAU6HnaJTk9lrRbEK-XinrLpsHa6PNHlOoGRTiEC9fmAg130 assertion
has provenance: NP57045.RAU6HnaJTk9lrRbEK-XinrLpsHa6PNHlOoGRTiEC9fmAg130 provenance
has publication info: NP57045.RAU6HnaJTk9lrRbEK-XinrLpsHa6PNHlOoGRTiEC9fmAg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57045.RAU6HnaJTk9lrRbEK-XinrLpsHa6PNHlOoGRTiEC9fmAg130 assertion
type: Assertion
description: [ These data suggest that variations in genes involved in immune regulation are associated with biologic and clinical phenotypes in the first year of life that might increase the risk for the subsequent development of childhood asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15007355
was generated by: ECO_0000203

NP57048.RAXspdBPyLs0IHJCxJ599mU8oOn891IVCL8 soDq2ryFU
has assertion: NP57048.RAXspdBPyLs0IHJCxJ599mU8oOn891IVCL8 soDq2ryFU130 assertion
has provenance: NP57048.RAXspdBPyLs0IHJCxJ599mU8oOn891IVCL8 soDq2ryFU130 provenance
has publication info: NP57048.RAXspdBPyLs0IHJCxJ599mU8oOn891IVCL8 soDq2ryFU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57048.RAXspdBPyLs0IHJCxJ599mU8oOn891IVCL8 soDq2ryFU130 assertion
type: Assertion
description: [These data provide a starting point for functional and genetic analysis of the IFNG genomic region in malaria and other infectious and inflammatory conditions affecting African populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15858598
was generated by: ECO_0000203

NP57049.RARJNgOkQePB PIWphD I0MLPFfGH-orN69EAV6GuvsFM
has assertion: NP57049.RARJNgOkQePB PIWphD I0MLPFfGH-orN69EAV6GuvsFM130 assertion
has provenance: NP57049.RARJNgOkQePB PIWphD I0MLPFfGH-orN69EAV6GuvsFM130 provenance
has publication info: NP57049.RARJNgOkQePB PIWphD I0MLPFfGH-orN69EAV6GuvsFM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57049.RARJNgOkQePB PIWphD I0MLPFfGH-orN69EAV6GuvsFM130 assertion
type: Assertion
description: [ Our findings indicate that heterogeneity in the promoter region of the IL-10 gene has a role in determining a spontaneous favourable outcome of HCV infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14698136
was generated by: ECO_0000203

NP57051.RAWf1OEFHVMSoUKW6XIjd8hTthS-pIoQKrN0Y sHfrWr0
has assertion: NP57051.RAWf1OEFHVMSoUKW6XIjd8hTthS-pIoQKrN0Y sHfrWr0130 assertion
has provenance: NP57051.RAWf1OEFHVMSoUKW6XIjd8hTthS-pIoQKrN0Y sHfrWr0130 provenance
has publication info: NP57051.RAWf1OEFHVMSoUKW6XIjd8hTthS-pIoQKrN0Y sHfrWr0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57051.RAWf1OEFHVMSoUKW6XIjd8hTthS-pIoQKrN0Y sHfrWr0130 assertion
type: Assertion
description: [In coeliac disease (CD) a profile of proinflammatory cytokines are secreted interferon gamma (IFNgamma) being one of the most important.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15215891
was generated by: ECO_0000203

NP57057.RARqyKRkjo6ugH1Cq9IritzUGfQiLUhNyh33DhT-Qa4Jk
has assertion: NP57057.RARqyKRkjo6ugH1Cq9IritzUGfQiLUhNyh33DhT-Qa4Jk130 assertion
has provenance: NP57057.RARqyKRkjo6ugH1Cq9IritzUGfQiLUhNyh33DhT-Qa4Jk130 provenance
has publication info: NP57057.RARqyKRkjo6ugH1Cq9IritzUGfQiLUhNyh33DhT-Qa4Jk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57057.RARqyKRkjo6ugH1Cq9IritzUGfQiLUhNyh33DhT-Qa4Jk130 assertion
type: Assertion
description: [These findings provide strong evidence of which IFN-gamma CA repeat and IRF-1 GT repeat polymorphisms influence the risk of asthma for children in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16961714
was generated by: ECO_0000203

NP57058.RATeJ4LZR2o0x9TPEUcc-DSbKSLhiDNIhRNLWL3GTH8DQ
has assertion: NP57058.RATeJ4LZR2o0x9TPEUcc-DSbKSLhiDNIhRNLWL3GTH8DQ130 assertion
has provenance: NP57058.RATeJ4LZR2o0x9TPEUcc-DSbKSLhiDNIhRNLWL3GTH8DQ130 provenance
has publication info: NP57058.RATeJ4LZR2o0x9TPEUcc-DSbKSLhiDNIhRNLWL3GTH8DQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57058.RATeJ4LZR2o0x9TPEUcc-DSbKSLhiDNIhRNLWL3GTH8DQ130 assertion
type: Assertion
description: [Our findings suggest that STAT-4 T90089C and IFN-gamma T874A polymorphisms might be the genetic factors for the risk of asthma in the Chinese population. In addition, the significant interactions among STAT-6 G2964A, STAT-4 T90089C and IFN-gamma T874A may increase an individuals susceptibility and contribute to the pathogenesis of asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17532201
was generated by: ECO_0000203

NP57059.RAWPuSXH8jxlivhlfcDi 8EsqmO7z1BF4WZ2Rwd9IvAqc
has assertion: NP57059.RAWPuSXH8jxlivhlfcDi 8EsqmO7z1BF4WZ2Rwd9IvAqc130 assertion
has provenance: NP57059.RAWPuSXH8jxlivhlfcDi 8EsqmO7z1BF4WZ2Rwd9IvAqc130 provenance
has publication info: NP57059.RAWPuSXH8jxlivhlfcDi 8EsqmO7z1BF4WZ2Rwd9IvAqc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57059.RAWPuSXH8jxlivhlfcDi 8EsqmO7z1BF4WZ2Rwd9IvAqc130 assertion
type: Assertion
description: [IL-10, TGF-beta, IL-2, IL-12, and IFN-gamma cytokine gene polymorphisms in asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18972297
was generated by: ECO_0000203

NP57061.RAT4tfs5jmPri2rtsKIb-eKgBjlemGfMPx7-n-ToqvR7Y
has assertion: NP57061.RAT4tfs5jmPri2rtsKIb-eKgBjlemGfMPx7-n-ToqvR7Y130 assertion
has provenance: NP57061.RAT4tfs5jmPri2rtsKIb-eKgBjlemGfMPx7-n-ToqvR7Y130 provenance
has publication info: NP57061.RAT4tfs5jmPri2rtsKIb-eKgBjlemGfMPx7-n-ToqvR7Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57061.RAT4tfs5jmPri2rtsKIb-eKgBjlemGfMPx7-n-ToqvR7Y130 assertion
type: Assertion
description: [The aims of the current investigation were to determine whether functional polymorphisms in the tumor necrosis factor-alpha (TNF-alpha) gene at positions -308 and -238; in the transforming growth factor-beta 1 (TGF-beta(1)) gene at positions -509, +869 (codon 10), and +915 (codon 25); in the interleukin-10 (IL-10) gene at position -1082; and in the intron 1 of the interferon-gamma (IFN-gamma) gene at position +874 are associated with alcoholic chronic pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15066699
was generated by: ECO_0000203

NP57064.RASJWtClqJ1LWZYNQe8FPYRrexD3oE-FvyXuq6tAhX-CE
has assertion: NP57064.RASJWtClqJ1LWZYNQe8FPYRrexD3oE-FvyXuq6tAhX-CE130 assertion
has provenance: NP57064.RASJWtClqJ1LWZYNQe8FPYRrexD3oE-FvyXuq6tAhX-CE130 provenance
has publication info: NP57064.RASJWtClqJ1LWZYNQe8FPYRrexD3oE-FvyXuq6tAhX-CE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57064.RASJWtClqJ1LWZYNQe8FPYRrexD3oE-FvyXuq6tAhX-CE130 assertion
type: Assertion
description: [It could be suggested that the genetic variation in IL-12 A/C (-1188) and IFN-gamma A/T (+874) cytokine genes could be risk factors for MS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19543959
was generated by: ECO_0000203

NP57068.RAf3lGp5FeC9Hu1KISZ ryRRiMHwFp3MS2PpAFvqEXEmw
has assertion: NP57068.RAf3lGp5FeC9Hu1KISZ ryRRiMHwFp3MS2PpAFvqEXEmw130 assertion
has provenance: NP57068.RAf3lGp5FeC9Hu1KISZ ryRRiMHwFp3MS2PpAFvqEXEmw130 provenance
has publication info: NP57068.RAf3lGp5FeC9Hu1KISZ ryRRiMHwFp3MS2PpAFvqEXEmw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57068.RAf3lGp5FeC9Hu1KISZ ryRRiMHwFp3MS2PpAFvqEXEmw130 assertion
type: Assertion
description: [Analysis of linkage and association of alleles of proinflammatory cytokines genes IL-6, IFNg and TNF with multiple sclerosis using transmission disequilibrium test (TDT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21090238
was generated by: ECO_0000203

NP57076.RAfUSuecPqjtwwdAVe2v nEiYgW91y5Y65ZAsxOGkSQoE
has assertion: NP57076.RAfUSuecPqjtwwdAVe2v nEiYgW91y5Y65ZAsxOGkSQoE130 assertion
has provenance: NP57076.RAfUSuecPqjtwwdAVe2v nEiYgW91y5Y65ZAsxOGkSQoE130 provenance
has publication info: NP57076.RAfUSuecPqjtwwdAVe2v nEiYgW91y5Y65ZAsxOGkSQoE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57076.RAfUSuecPqjtwwdAVe2v nEiYgW91y5Y65ZAsxOGkSQoE130 assertion
type: Assertion
description: [To explore the relationship between cytokines (tumor necrosis factor-alpha, interferon-gamma, interleukin-4 and interleukin-10), which expressed abnormal quantity in the peripheral blood to intrauterine hepatitis B virus infectious children, gene single nucleotide polymorphism (SNP) and susceptibility to hepatitis B virus intrauterine infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16232344
was generated by: ECO_0000203

NP57079.RAYy4q8F1AMfoP4nUPg5J8nwmHaP2W8eY-YC11cVvAVbE
has assertion: NP57079.RAYy4q8F1AMfoP4nUPg5J8nwmHaP2W8eY-YC11cVvAVbE130 assertion
has provenance: NP57079.RAYy4q8F1AMfoP4nUPg5J8nwmHaP2W8eY-YC11cVvAVbE130 provenance
has publication info: NP57079.RAYy4q8F1AMfoP4nUPg5J8nwmHaP2W8eY-YC11cVvAVbE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57079.RAYy4q8F1AMfoP4nUPg5J8nwmHaP2W8eY-YC11cVvAVbE130 assertion
type: Assertion
description: [ This study suggested the possibility that TNF-alpha-238 A allele and IFN-gamma + 874 A allele were associated with HBV intrauterine infection. There was no evident relationship between IL-4-590 C/T allele SNP and susceptibility to HBV intrauterine infection, but the IL-10-1082 G allele seemed to be associated with preventive efficacy to HBV intrauterine infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15941525
was generated by: ECO_0000203

NP57080.RAVF4 M90lxbYhR4sBCYFUqGvMb3IAW4sxPl1Mll8lqWA
has assertion: NP57080.RAVF4 M90lxbYhR4sBCYFUqGvMb3IAW4sxPl1Mll8lqWA130 assertion
has provenance: NP57080.RAVF4 M90lxbYhR4sBCYFUqGvMb3IAW4sxPl1Mll8lqWA130 provenance
has publication info: NP57080.RAVF4 M90lxbYhR4sBCYFUqGvMb3IAW4sxPl1Mll8lqWA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57080.RAVF4 M90lxbYhR4sBCYFUqGvMb3IAW4sxPl1Mll8lqWA130 assertion
type: Assertion
description: [Association of interferon-gamma gene haplotype in the Chinese population with hepatitis B virus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17033822
was generated by: ECO_0000203

NP57081.RAZYeOxBVB1bT00ch-LIEDEJlB4IJJx4L3GI8ai7oarwQ
has assertion: NP57081.RAZYeOxBVB1bT00ch-LIEDEJlB4IJJx4L3GI8ai7oarwQ130 assertion
has provenance: NP57081.RAZYeOxBVB1bT00ch-LIEDEJlB4IJJx4L3GI8ai7oarwQ130 provenance
has publication info: NP57081.RAZYeOxBVB1bT00ch-LIEDEJlB4IJJx4L3GI8ai7oarwQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57081.RAZYeOxBVB1bT00ch-LIEDEJlB4IJJx4L3GI8ai7oarwQ130 assertion
type: Assertion
description: [Association of cytokine genetic polymorphism with hepatitis B infection evolution in adult patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17612762
was generated by: ECO_0000203

NP57085.RAS-PKxRxqmlU i5hkLOZfj2W8OAqpwOYFYdCQNTCpTR4
has assertion: NP57085.RAS-PKxRxqmlU i5hkLOZfj2W8OAqpwOYFYdCQNTCpTR4130 assertion
has provenance: NP57085.RAS-PKxRxqmlU i5hkLOZfj2W8OAqpwOYFYdCQNTCpTR4130 provenance
has publication info: NP57085.RAS-PKxRxqmlU i5hkLOZfj2W8OAqpwOYFYdCQNTCpTR4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57085.RAS-PKxRxqmlU i5hkLOZfj2W8OAqpwOYFYdCQNTCpTR4130 assertion
type: Assertion
description: [ The cytokine gene polymorphisms studied here do not appear to influence IBD susceptibility. There does, however, appear to be an influence on disease phenotype, particularly on CD site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15842590
was generated by: ECO_0000203

NP57087.RAQbqy-VsMHT8ld0oe4R9QeVn 4hAT9KhETaMgJ3dZyHE
has assertion: NP57087.RAQbqy-VsMHT8ld0oe4R9QeVn 4hAT9KhETaMgJ3dZyHE130 assertion
has provenance: NP57087.RAQbqy-VsMHT8ld0oe4R9QeVn 4hAT9KhETaMgJ3dZyHE130 provenance
has publication info: NP57087.RAQbqy-VsMHT8ld0oe4R9QeVn 4hAT9KhETaMgJ3dZyHE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57087.RAQbqy-VsMHT8ld0oe4R9QeVn 4hAT9KhETaMgJ3dZyHE130 assertion
type: Assertion
description: [Functional IFNG polymorphism in intron 1 in association with an increased risk to promote sporadic breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15900487
was generated by: ECO_0000203

NP57090.RAXzumz04KQ4g5WabuZMyNkIEpRtmelQm64q1J-DCCfN0
has assertion: NP57090.RAXzumz04KQ4g5WabuZMyNkIEpRtmelQm64q1J-DCCfN0130 assertion
has provenance: NP57090.RAXzumz04KQ4g5WabuZMyNkIEpRtmelQm64q1J-DCCfN0130 provenance
has publication info: NP57090.RAXzumz04KQ4g5WabuZMyNkIEpRtmelQm64q1J-DCCfN0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57090.RAXzumz04KQ4g5WabuZMyNkIEpRtmelQm64q1J-DCCfN0130 assertion
type: Assertion
description: [further studies involving larger numbers of subjects are required.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17261759
was generated by: ECO_0000203

NP57096.RAfZbilM0SUP9DTD-VOiLzcr5fdOflfxOQcAJXGx Yx2Y
has assertion: NP57096.RAfZbilM0SUP9DTD-VOiLzcr5fdOflfxOQcAJXGx Yx2Y130 assertion
has provenance: NP57096.RAfZbilM0SUP9DTD-VOiLzcr5fdOflfxOQcAJXGx Yx2Y130 provenance
has publication info: NP57096.RAfZbilM0SUP9DTD-VOiLzcr5fdOflfxOQcAJXGx Yx2Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57096.RAfZbilM0SUP9DTD-VOiLzcr5fdOflfxOQcAJXGx Yx2Y130 assertion
type: Assertion
description: [IL-10 and IL-6 gene polymorphisms as potential host susceptibility factors in Brucellosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17544674
was generated by: ECO_0000203

NP57097.RAfN2UlD0eA2Fuj2UYJDTGTnmgbxuptaGGgmx8y1KZVpM
has assertion: NP57097.RAfN2UlD0eA2Fuj2UYJDTGTnmgbxuptaGGgmx8y1KZVpM130 assertion
has provenance: NP57097.RAfN2UlD0eA2Fuj2UYJDTGTnmgbxuptaGGgmx8y1KZVpM130 provenance
has publication info: NP57097.RAfN2UlD0eA2Fuj2UYJDTGTnmgbxuptaGGgmx8y1KZVpM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57097.RAfN2UlD0eA2Fuj2UYJDTGTnmgbxuptaGGgmx8y1KZVpM130 assertion
type: Assertion
description: [Given that the production of IFN-gamma and IL-4 are under genetic control, we investigated the relationship between these two cytokine gene polymorphisms and the susceptibility to brucellosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17566759
was generated by: ECO_0000203

NP57098.RAVolf8piEox-EAl8j3jDG8t3trc8mNlfVyZxkkSPmiPg
has assertion: NP57098.RAVolf8piEox-EAl8j3jDG8t3trc8mNlfVyZxkkSPmiPg130 assertion
has provenance: NP57098.RAVolf8piEox-EAl8j3jDG8t3trc8mNlfVyZxkkSPmiPg130 provenance
has publication info: NP57098.RAVolf8piEox-EAl8j3jDG8t3trc8mNlfVyZxkkSPmiPg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57098.RAVolf8piEox-EAl8j3jDG8t3trc8mNlfVyZxkkSPmiPg130 assertion
type: Assertion
description: [TNF-alpha, TGF-beta, IL-10, IL-6 and IFN-gamma gene polymorphisms as risk factors for brucellosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19579695
was generated by: ECO_0000203

NP57107.RAUhWIGqHZ64LXlkKBLyuEYSwazndVL6v-YxKPVsAv7FQ
has assertion: NP57107.RAUhWIGqHZ64LXlkKBLyuEYSwazndVL6v-YxKPVsAv7FQ130 assertion
has provenance: NP57107.RAUhWIGqHZ64LXlkKBLyuEYSwazndVL6v-YxKPVsAv7FQ130 provenance
has publication info: NP57107.RAUhWIGqHZ64LXlkKBLyuEYSwazndVL6v-YxKPVsAv7FQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57107.RAUhWIGqHZ64LXlkKBLyuEYSwazndVL6v-YxKPVsAv7FQ130 assertion
type: Assertion
description: [Interferon-gamma polymorphisms correlate with duration of survival in pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15556691
was generated by: ECO_0000203

NP57123.RAYHsZCnwdHx14G5D7Q2xulmXQW1yEMncBV 9kAd-nTDI
has assertion: NP57123.RAYHsZCnwdHx14G5D7Q2xulmXQW1yEMncBV 9kAd-nTDI130 assertion
has provenance: NP57123.RAYHsZCnwdHx14G5D7Q2xulmXQW1yEMncBV 9kAd-nTDI130 provenance
has publication info: NP57123.RAYHsZCnwdHx14G5D7Q2xulmXQW1yEMncBV 9kAd-nTDI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57123.RAYHsZCnwdHx14G5D7Q2xulmXQW1yEMncBV 9kAd-nTDI130 assertion
type: Assertion
description: [But these SNPs did not show a clinical significance, as compared with the GT-repeat in IFNAR1, in the context of interferon responsiveness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12697242
was generated by: ECO_0000203

NP57127.RAQCpuyRf 27eLZjvc0hV vaYAAR YFdiyH-TDREOtXQ8
has assertion: NP57127.RAQCpuyRf 27eLZjvc0hV vaYAAR YFdiyH-TDREOtXQ8130 assertion
has provenance: NP57127.RAQCpuyRf 27eLZjvc0hV vaYAAR YFdiyH-TDREOtXQ8130 provenance
has publication info: NP57127.RAQCpuyRf 27eLZjvc0hV vaYAAR YFdiyH-TDREOtXQ8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57127.RAQCpuyRf 27eLZjvc0hV vaYAAR YFdiyH-TDREOtXQ8130 assertion
type: Assertion
description: [ This preliminary result suggests that the promoter GT repeat dinucleotide microsatellite polymorphism of the IFNAR1 gene may represent a risk factor for the development of depressive symptoms during IFN-alpha therapy for hepatitis C and other conditions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15990456
was generated by: ECO_0000203

NP57130.RAVbbLM0IYrp80rAm5-JgCk3RgVqGS4FM9gAn9-xObk2A
has assertion: NP57130.RAVbbLM0IYrp80rAm5-JgCk3RgVqGS4FM9gAn9-xObk2A130 assertion
has provenance: NP57130.RAVbbLM0IYrp80rAm5-JgCk3RgVqGS4FM9gAn9-xObk2A130 provenance
has publication info: NP57130.RAVbbLM0IYrp80rAm5-JgCk3RgVqGS4FM9gAn9-xObk2A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57130.RAVbbLM0IYrp80rAm5-JgCk3RgVqGS4FM9gAn9-xObk2A130 assertion
type: Assertion
description: [The results of this study suggest that the 184Ile homozygote of the IFNA17 gene may represent an important susceptibility biomarker for cervical cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12490311
was generated by: ECO_0000203

NP57134.RAUL 3FdKUHr1vnb rFrm-FA5SLlPRcvDnx6UYdnIrY9U
has assertion: NP57134.RAUL 3FdKUHr1vnb rFrm-FA5SLlPRcvDnx6UYdnIrY9U130 assertion
has provenance: NP57134.RAUL 3FdKUHr1vnb rFrm-FA5SLlPRcvDnx6UYdnIrY9U130 provenance
has publication info: NP57134.RAUL 3FdKUHr1vnb rFrm-FA5SLlPRcvDnx6UYdnIrY9U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57134.RAUL 3FdKUHr1vnb rFrm-FA5SLlPRcvDnx6UYdnIrY9U130 assertion
type: Assertion
description: [Genotyping of single nucleotide polymorphisms (SNPs) in the IDE gene in Finnish patients with AD and controls revealed SNPs rs4646953 and rs4646955 to be associated with AD, conferring an approximately two-fold increased risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17496198
was generated by: ECO_0000203

NP57135.RAQnkPstJSU5LLgX0pSjo 7F7OtWjWliaZvzwH0NHBgQ8
has assertion: NP57135.RAQnkPstJSU5LLgX0pSjo 7F7OtWjWliaZvzwH0NHBgQ8130 assertion
has provenance: NP57135.RAQnkPstJSU5LLgX0pSjo 7F7OtWjWliaZvzwH0NHBgQ8130 provenance
has publication info: NP57135.RAQnkPstJSU5LLgX0pSjo 7F7OtWjWliaZvzwH0NHBgQ8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57135.RAQnkPstJSU5LLgX0pSjo 7F7OtWjWliaZvzwH0NHBgQ8130 assertion
type: Assertion
description: [Combined risk effects of IDE and NEP gene variants on Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19864659
was generated by: ECO_0000203

NP57137.RAfShubWxiQJfmGWAoVd531G9IezMQsWokW6UuULKg8dk
has assertion: NP57137.RAfShubWxiQJfmGWAoVd531G9IezMQsWokW6UuULKg8dk130 assertion
has provenance: NP57137.RAfShubWxiQJfmGWAoVd531G9IezMQsWokW6UuULKg8dk130 provenance
has publication info: NP57137.RAfShubWxiQJfmGWAoVd531G9IezMQsWokW6UuULKg8dk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57137.RAfShubWxiQJfmGWAoVd531G9IezMQsWokW6UuULKg8dk130 assertion
type: Assertion
description: [Promoter polymorphisms which modulate insulin degrading enzyme expression may increase susceptibility to Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18996360
was generated by: ECO_0000203

NP57139.RAcG lCK2pt3XsAc osgOfMxISwuqtS5eCapZH4b72 8k
has assertion: NP57139.RAcG lCK2pt3XsAc osgOfMxISwuqtS5eCapZH4b72 8k130 assertion
has provenance: NP57139.RAcG lCK2pt3XsAc osgOfMxISwuqtS5eCapZH4b72 8k130 provenance
has publication info: NP57139.RAcG lCK2pt3XsAc osgOfMxISwuqtS5eCapZH4b72 8k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57139.RAcG lCK2pt3XsAc osgOfMxISwuqtS5eCapZH4b72 8k130 assertion
type: Assertion
description: [Positive association between risk for late-onset Alzheimer disease and genetic variation in IDE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16876916
was generated by: ECO_0000203

NP57149.RAbZOsFccAS3qdTtU1p9YP6Rb-wgd8ZArvn0QIy4PUl1Y
has assertion: NP57149.RAbZOsFccAS3qdTtU1p9YP6Rb-wgd8ZArvn0QIy4PUl1Y130 assertion
has provenance: NP57149.RAbZOsFccAS3qdTtU1p9YP6Rb-wgd8ZArvn0QIy4PUl1Y130 provenance
has publication info: NP57149.RAbZOsFccAS3qdTtU1p9YP6Rb-wgd8ZArvn0QIy4PUl1Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57149.RAbZOsFccAS3qdTtU1p9YP6Rb-wgd8ZArvn0QIy4PUl1Y130 assertion
type: Assertion
description: [Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12082592
was generated by: ECO_0000203

NP57153.RAYqOGitE6-T3dhW4rc qQH0nuLCe96plFFTvmdGGlht4
has assertion: NP57153.RAYqOGitE6-T3dhW4rc qQH0nuLCe96plFFTvmdGGlht4130 assertion
has provenance: NP57153.RAYqOGitE6-T3dhW4rc qQH0nuLCe96plFFTvmdGGlht4130 provenance
has publication info: NP57153.RAYqOGitE6-T3dhW4rc qQH0nuLCe96plFFTvmdGGlht4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57153.RAYqOGitE6-T3dhW4rc qQH0nuLCe96plFFTvmdGGlht4130 assertion
type: Assertion
description: [Genetic approaches to the investigation of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11981324
was generated by: ECO_0000203

NP57155.RAdlEWKc7GJFh6UUo4ikNrYM1ELZFSe-JLnqCUpljs2SM
has assertion: NP57155.RAdlEWKc7GJFh6UUo4ikNrYM1ELZFSe-JLnqCUpljs2SM130 assertion
has provenance: NP57155.RAdlEWKc7GJFh6UUo4ikNrYM1ELZFSe-JLnqCUpljs2SM130 provenance
has publication info: NP57155.RAdlEWKc7GJFh6UUo4ikNrYM1ELZFSe-JLnqCUpljs2SM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57155.RAdlEWKc7GJFh6UUo4ikNrYM1ELZFSe-JLnqCUpljs2SM130 assertion
type: Assertion
description: [The effect observed was found to be strongest among the HLA-DQB1*0602-positive subjects, which implies genetic heterogeneity of MS. Meta-analysis of all published datasets supports increased risk of MS for the ICAM-1 Lys(469) homozygotes (relative risk = 1.3, p = 0.002).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12590979
was generated by: ECO_0000203

NP57163.RASNEiJCLjsj9jjVpOje8M3qyrfWalRQplaKnOn3vlGsg
has assertion: NP57163.RASNEiJCLjsj9jjVpOje8M3qyrfWalRQplaKnOn3vlGsg130 assertion
has provenance: NP57163.RASNEiJCLjsj9jjVpOje8M3qyrfWalRQplaKnOn3vlGsg130 provenance
has publication info: NP57163.RASNEiJCLjsj9jjVpOje8M3qyrfWalRQplaKnOn3vlGsg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57163.RASNEiJCLjsj9jjVpOje8M3qyrfWalRQplaKnOn3vlGsg130 assertion
type: Assertion
description: [Polymerase chain reaction-sequence specific primers (PCR-SSP) technology and PCR-restriction fragment length polymorphism(PCR-RFLP) were used for the detection of ICAM-1 genotypes in 165 patients with MI(including acute MI and old MI) and 199 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16471223
was generated by: ECO_0000203

NP57164.RATJ3xNDwXEEzNU51upYODBWIkrJQ5ryZwD6d9mRnR1vo
has assertion: NP57164.RATJ3xNDwXEEzNU51upYODBWIkrJQ5ryZwD6d9mRnR1vo130 assertion
has provenance: NP57164.RATJ3xNDwXEEzNU51upYODBWIkrJQ5ryZwD6d9mRnR1vo130 provenance
has publication info: NP57164.RATJ3xNDwXEEzNU51upYODBWIkrJQ5ryZwD6d9mRnR1vo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57164.RATJ3xNDwXEEzNU51upYODBWIkrJQ5ryZwD6d9mRnR1vo130 assertion
type: Assertion
description: [Functional genetic variants in cytokine and leukocyte-endothelial interaction pathways are independently associated with severity of myonecrosis after cardiac surgery. This may aid in preoperative identification of high-risk cardiac surgical patients and development of novel cardioprotective strategies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16820586
was generated by: ECO_0000203

NP57168.RAas-RSyGUPrtGIXjPksgGjOHanFhd8FDnP5n2k58-ZKs
has assertion: NP57168.RAas-RSyGUPrtGIXjPksgGjOHanFhd8FDnP5n2k58-ZKs130 assertion
has provenance: NP57168.RAas-RSyGUPrtGIXjPksgGjOHanFhd8FDnP5n2k58-ZKs130 provenance
has publication info: NP57168.RAas-RSyGUPrtGIXjPksgGjOHanFhd8FDnP5n2k58-ZKs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57168.RAas-RSyGUPrtGIXjPksgGjOHanFhd8FDnP5n2k58-ZKs130 assertion
type: Assertion
description: [Evidence from autopsy and in vitro binding studies suggests that adhesion of erythrocytes infected with Plasmodium falciparum to the human host intercellular adhesion molecule (ICAM)-1 receptor is important in the pathogenesis of severe malaria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18528404
was generated by: ECO_0000203

NP57169.RAS75EsnW hTA82CGMhjh0515vP EXJ8VsI1hltoVWk1M
has assertion: NP57169.RAS75EsnW hTA82CGMhjh0515vP EXJ8VsI1hltoVWk1M130 assertion
has provenance: NP57169.RAS75EsnW hTA82CGMhjh0515vP EXJ8VsI1hltoVWk1M130 provenance
has publication info: NP57169.RAS75EsnW hTA82CGMhjh0515vP EXJ8VsI1hltoVWk1M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57169.RAS75EsnW hTA82CGMhjh0515vP EXJ8VsI1hltoVWk1M130 assertion
type: Assertion
description: [In a study sample specifically selected for the characteristic of a family history of premature coronary heart disease, ICAM K469E GG was associated with lower CAC scores in men but not women even after controlling for plasma levels of sICAM-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15682683
was generated by: ECO_0000203

NP57170.RAaw3ScvdqbzWDzNKVH qGKb1PVDh3LtLxPvgIrdT2wzY
has assertion: NP57170.RAaw3ScvdqbzWDzNKVH qGKb1PVDh3LtLxPvgIrdT2wzY130 assertion
has provenance: NP57170.RAaw3ScvdqbzWDzNKVH qGKb1PVDh3LtLxPvgIrdT2wzY130 provenance
has publication info: NP57170.RAaw3ScvdqbzWDzNKVH qGKb1PVDh3LtLxPvgIrdT2wzY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57170.RAaw3ScvdqbzWDzNKVH qGKb1PVDh3LtLxPvgIrdT2wzY130 assertion
type: Assertion
description: [ In conclusion, contemporaneous carrier-state of two or three polymorphic variants within analyzed genes is associated with CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16043164
was generated by: ECO_0000203

NP57172.RAcUCxvYaqTv-zb80fxb3bdH5xrdRUm8u6N-kzrATBrmU
has assertion: NP57172.RAcUCxvYaqTv-zb80fxb3bdH5xrdRUm8u6N-kzrATBrmU130 assertion
has provenance: NP57172.RAcUCxvYaqTv-zb80fxb3bdH5xrdRUm8u6N-kzrATBrmU130 provenance
has publication info: NP57172.RAcUCxvYaqTv-zb80fxb3bdH5xrdRUm8u6N-kzrATBrmU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57172.RAcUCxvYaqTv-zb80fxb3bdH5xrdRUm8u6N-kzrATBrmU130 assertion
type: Assertion
description: [There is the polymorphism of ICAM1 K469E gene in Han population of China, and the K allele may be a genetic factor influencing the risk of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16604496
was generated by: ECO_0000203

NP57180.RAWjrUlT6vYVH08gHRC6DG v30BXylGxwYpmNaCRb13Sk
has assertion: NP57180.RAWjrUlT6vYVH08gHRC6DG v30BXylGxwYpmNaCRb13Sk130 assertion
has provenance: NP57180.RAWjrUlT6vYVH08gHRC6DG v30BXylGxwYpmNaCRb13Sk130 provenance
has publication info: NP57180.RAWjrUlT6vYVH08gHRC6DG v30BXylGxwYpmNaCRb13Sk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57180.RAWjrUlT6vYVH08gHRC6DG v30BXylGxwYpmNaCRb13Sk130 assertion
type: Assertion
description: [We hypothesize that the biochemical effect of the G241A SNP is masked in schizophrenic patients, indicating a disease-related mechanism leading to reduced levels of sICAM-1 in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15756053
was generated by: ECO_0000203

NP57183.RAXZniXVAKc2hFuI-clYvE2jz6WOZc7MOqWR4fuIrFlqU
has assertion: NP57183.RAXZniXVAKc2hFuI-clYvE2jz6WOZc7MOqWR4fuIrFlqU130 assertion
has provenance: NP57183.RAXZniXVAKc2hFuI-clYvE2jz6WOZc7MOqWR4fuIrFlqU130 provenance
has publication info: NP57183.RAXZniXVAKc2hFuI-clYvE2jz6WOZc7MOqWR4fuIrFlqU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57183.RAXZniXVAKc2hFuI-clYvE2jz6WOZc7MOqWR4fuIrFlqU130 assertion
type: Assertion
description: [In proliferative diabetic retinopathy (PDR) increased levels of cytokines, inflammatory cells and angiogenic factors are present.These factors increase the expression of cellular adhesion molecules (CAMs)The objective of this study was to investigate the association between the polymorphisms of the ICAM-1 gene (K469E, G241A) and the development of PDR among patients with type 2 diabetes in the Slovenian population (Caucasians).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18942221
was generated by: ECO_0000203

NP57186.RAeSx807b7GOcMf5T-wlgMMXsasvTHkAfxbfs7phDhmKk
has assertion: NP57186.RAeSx807b7GOcMf5T-wlgMMXsasvTHkAfxbfs7phDhmKk130 assertion
has provenance: NP57186.RAeSx807b7GOcMf5T-wlgMMXsasvTHkAfxbfs7phDhmKk130 provenance
has publication info: NP57186.RAeSx807b7GOcMf5T-wlgMMXsasvTHkAfxbfs7phDhmKk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57186.RAeSx807b7GOcMf5T-wlgMMXsasvTHkAfxbfs7phDhmKk130 assertion
type: Assertion
description: [The independent risk conferred by genetic variants encoding pathways such as inflammation and lipid metabolism, not adequately reflected by conventional biomarkers, may identify high-risk individuals for intensified control of modifiable risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20536507
was generated by: ECO_0000203

NP57189.RAd4A2BYb7myyoMZ9dgBL9YjjO3hs2y5EhxQDp3cVjBow
has assertion: NP57189.RAd4A2BYb7myyoMZ9dgBL9YjjO3hs2y5EhxQDp3cVjBow130 assertion
has provenance: NP57189.RAd4A2BYb7myyoMZ9dgBL9YjjO3hs2y5EhxQDp3cVjBow130 provenance
has publication info: NP57189.RAd4A2BYb7myyoMZ9dgBL9YjjO3hs2y5EhxQDp3cVjBow130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57189.RAd4A2BYb7myyoMZ9dgBL9YjjO3hs2y5EhxQDp3cVjBow130 assertion
type: Assertion
description: [Our aim was to investigate the prevalence of polymorphisms in NOD2, ICAM-1 and CCR5 genes in Czech and Slovak patients with IBD in comparison with healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18647548
was generated by: ECO_0000203

NP57190.RAQpwSFI1IqKkHEWKrxMDhGhbLaKM0r6YiRPV PIj-pAA
has assertion: NP57190.RAQpwSFI1IqKkHEWKrxMDhGhbLaKM0r6YiRPV PIj-pAA130 assertion
has provenance: NP57190.RAQpwSFI1IqKkHEWKrxMDhGhbLaKM0r6YiRPV PIj-pAA130 provenance
has publication info: NP57190.RAQpwSFI1IqKkHEWKrxMDhGhbLaKM0r6YiRPV PIj-pAA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57190.RAQpwSFI1IqKkHEWKrxMDhGhbLaKM0r6YiRPV PIj-pAA130 assertion
type: Assertion
description: [Polymorphism in ICAM-1, PECAM-1, E-selectin, and L-selectin genes in Tunisian patients with inflammatory bowel disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19212205
was generated by: ECO_0000203

NP57202.RAf9gZHfR0ifl2QaP2aUs2pXSZR82gsue583-aS8p9 Nc
has assertion: NP57202.RAf9gZHfR0ifl2QaP2aUs2pXSZR82gsue583-aS8p9 Nc130 assertion
has provenance: NP57202.RAf9gZHfR0ifl2QaP2aUs2pXSZR82gsue583-aS8p9 Nc130 provenance
has publication info: NP57202.RAf9gZHfR0ifl2QaP2aUs2pXSZR82gsue583-aS8p9 Nc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57202.RAf9gZHfR0ifl2QaP2aUs2pXSZR82gsue583-aS8p9 Nc130 assertion
type: Assertion
description: [Polymorphisms in the oxygen-regulated protein 150 gene (ORP150) are associated with insulin resistance in Pima Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11978664
was generated by: ECO_0000203

NP57209.RAWQAAptJB Idn03-w4j87K8zA5rdI9rnjlRzHi7xXmMQ
has assertion: NP57209.RAWQAAptJB Idn03-w4j87K8zA5rdI9rnjlRzHi7xXmMQ130 assertion
has provenance: NP57209.RAWQAAptJB Idn03-w4j87K8zA5rdI9rnjlRzHi7xXmMQ130 provenance
has publication info: NP57209.RAWQAAptJB Idn03-w4j87K8zA5rdI9rnjlRzHi7xXmMQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57209.RAWQAAptJB Idn03-w4j87K8zA5rdI9rnjlRzHi7xXmMQ130 assertion
type: Assertion
description: [To assess the associations between schizophrenia and six functional genes: dopamine D2 receptor gene (DRD2), dopamine D4 receptor gene (DRD4), 5-hydroxytryptamine 2A receptor gene (5-HT2A), 5-HT6 receptor gene (5-HT6), catechol-O-methyltransferase gene (COMT) and dopamine transporter gene (DAT1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12579508
was generated by: ECO_0000203

NP57210.RAW9IqzrFaYbYN-iHNpKfdnyF1G6YLNmHDVqeydR4OQxY
has assertion: NP57210.RAW9IqzrFaYbYN-iHNpKfdnyF1G6YLNmHDVqeydR4OQxY130 assertion
has provenance: NP57210.RAW9IqzrFaYbYN-iHNpKfdnyF1G6YLNmHDVqeydR4OQxY130 provenance
has publication info: NP57210.RAW9IqzrFaYbYN-iHNpKfdnyF1G6YLNmHDVqeydR4OQxY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57210.RAW9IqzrFaYbYN-iHNpKfdnyF1G6YLNmHDVqeydR4OQxY130 assertion
type: Assertion
description: [In conclusion, the 5HT(6) receptor gene variant can affect risperidone response to positive symptoms and general psychopathology (but not negative symptoms) after control for nongenetic factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14741325
was generated by: ECO_0000203

NP57215.RAQfsXSnPzDpGdD1FoBVuL2XbhXQYV07h7xq7jfwmE4bI
has assertion: NP57215.RAQfsXSnPzDpGdD1FoBVuL2XbhXQYV07h7xq7jfwmE4bI130 assertion
has provenance: NP57215.RAQfsXSnPzDpGdD1FoBVuL2XbhXQYV07h7xq7jfwmE4bI130 provenance
has publication info: NP57215.RAQfsXSnPzDpGdD1FoBVuL2XbhXQYV07h7xq7jfwmE4bI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57215.RAQfsXSnPzDpGdD1FoBVuL2XbhXQYV07h7xq7jfwmE4bI130 assertion
type: Assertion
description: [These data suggest that the HTR6 polymorphism C267T possibly involved in the susceptibility to LOAD as an APOE varepsilon4-allele independent risk factor of LOAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15531082
was generated by: ECO_0000203

NP57220.RAd8gSXgnqT hdchOaHZMSwmeBYG5TMAfzViY2uM FeVg
has assertion: NP57220.RAd8gSXgnqT hdchOaHZMSwmeBYG5TMAfzViY2uM FeVg130 assertion
has provenance: NP57220.RAd8gSXgnqT hdchOaHZMSwmeBYG5TMAfzViY2uM FeVg130 provenance
has publication info: NP57220.RAd8gSXgnqT hdchOaHZMSwmeBYG5TMAfzViY2uM FeVg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57220.RAd8gSXgnqT hdchOaHZMSwmeBYG5TMAfzViY2uM FeVg130 assertion
type: Assertion
description: [These polymorphisms probably do not represent major genetic risk factors of AD. However, further studies including other genetic variants of the serotonergic neurotransmitter system are needed in order to elucidate their role in AD. ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11692286
was generated by: ECO_0000203

NP57223.RAUQ-ghIlP 4rhgvxG4oqlt7bfbHbvo0SF5vZex-E7j2w
has assertion: NP57223.RAUQ-ghIlP 4rhgvxG4oqlt7bfbHbvo0SF5vZex-E7j2w130 assertion
has provenance: NP57223.RAUQ-ghIlP 4rhgvxG4oqlt7bfbHbvo0SF5vZex-E7j2w130 provenance
has publication info: NP57223.RAUQ-ghIlP 4rhgvxG4oqlt7bfbHbvo0SF5vZex-E7j2w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57223.RAUQ-ghIlP 4rhgvxG4oqlt7bfbHbvo0SF5vZex-E7j2w130 assertion
type: Assertion
description: [In this study, we evaluated the association of seven serotonin signal transduction-linked single nucleotide polymorphisms HTR1A (rs6295), HTR2A (rs6313, rs6311 and rs7997012), HTR6 (rs1805054), TPH1 (rs1800532) and TPH2 (rs1386494) with major depressive disorder and/or treatment outcome with serotonin reuptake inhibitors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19590397
was generated by: ECO_0000203

NP57227.RASpKu1vGE9crtuut9LV8pe9xGr84kQzLLGtRuaJ0g6AU
has assertion: NP57227.RASpKu1vGE9crtuut9LV8pe9xGr84kQzLLGtRuaJ0g6AU130 assertion
has provenance: NP57227.RASpKu1vGE9crtuut9LV8pe9xGr84kQzLLGtRuaJ0g6AU130 provenance
has publication info: NP57227.RASpKu1vGE9crtuut9LV8pe9xGr84kQzLLGtRuaJ0g6AU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57227.RASpKu1vGE9crtuut9LV8pe9xGr84kQzLLGtRuaJ0g6AU130 assertion
type: Assertion
description: [These findings suggest that genomic variations in the HTR4 gene may confer susceptibility to mood disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12399948
was generated by: ECO_0000203

NP57229.RAdNe2Bo2uprgGDx11kuxgqpDRiuTIdw Yk9K 334nEX4
has assertion: NP57229.RAdNe2Bo2uprgGDx11kuxgqpDRiuTIdw Yk9K 334nEX4130 assertion
has provenance: NP57229.RAdNe2Bo2uprgGDx11kuxgqpDRiuTIdw Yk9K 334nEX4130 provenance
has publication info: NP57229.RAdNe2Bo2uprgGDx11kuxgqpDRiuTIdw Yk9K 334nEX4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57229.RAdNe2Bo2uprgGDx11kuxgqpDRiuTIdw Yk9K 334nEX4130 assertion
type: Assertion
description: [Of these, four polymorphisms at or in close proximity to exon d, g.83097C/T (HTR4-SVR (splice variant region) SNP1), g.83159G/A (HTR4-SVRSNP2), g.83164 (T)9-10 (HTR4-SVRSNP3), and g.83198A/G (HTR4-SVRSNP4), showed significant association with bipolar disorder with odds ratios of 1.5 to 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12399948
was generated by: ECO_0000203

NP57232.RAcUDJI44nGRSPBje7v-Pt4Ggx4i 2sqfzEWZdtpDJJEM
has assertion: NP57232.RAcUDJI44nGRSPBje7v-Pt4Ggx4i 2sqfzEWZdtpDJJEM130 assertion
has provenance: NP57232.RAcUDJI44nGRSPBje7v-Pt4Ggx4i 2sqfzEWZdtpDJJEM130 provenance
has publication info: NP57232.RAcUDJI44nGRSPBje7v-Pt4Ggx4i 2sqfzEWZdtpDJJEM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57232.RAcUDJI44nGRSPBje7v-Pt4Ggx4i 2sqfzEWZdtpDJJEM130 assertion
type: Assertion
description: [These findings show that the C178T(Pro16Ser) variant in HTR3A may represent a functional variant and affect the susceptibility to bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11505217
was generated by: ECO_0000203

NP57236.RAZOi74kBtwyAa3RI0PCTshhyPfjC45TPqXZluP7ZRy-c
has assertion: NP57236.RAZOi74kBtwyAa3RI0PCTshhyPfjC45TPqXZluP7ZRy-c130 assertion
has provenance: NP57236.RAZOi74kBtwyAa3RI0PCTshhyPfjC45TPqXZluP7ZRy-c130 provenance
has publication info: NP57236.RAZOi74kBtwyAa3RI0PCTshhyPfjC45TPqXZluP7ZRy-c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57236.RAZOi74kBtwyAa3RI0PCTshhyPfjC45TPqXZluP7ZRy-c130 assertion
type: Assertion
description: [These findings show that the C178T(Pro16Ser) variant in HTR3A may represent a functional variant and affect the susceptibility to bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11505217
was generated by: ECO_0000203

NP57246.RASxydviCXm FPcHwVcJkYUrzmtfpBhPdDOgaH-Ux W0E
has assertion: NP57246.RASxydviCXm FPcHwVcJkYUrzmtfpBhPdDOgaH-Ux W0E130 assertion
has provenance: NP57246.RASxydviCXm FPcHwVcJkYUrzmtfpBhPdDOgaH-Ux W0E130 provenance
has publication info: NP57246.RASxydviCXm FPcHwVcJkYUrzmtfpBhPdDOgaH-Ux W0E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57246.RASxydviCXm FPcHwVcJkYUrzmtfpBhPdDOgaH-Ux W0E130 assertion
type: Assertion
description: [ The present results suggest that the HTR3A and DBH genes may participate in the regulation of dopamine and serotonin turnover rates in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15102340
was generated by: ECO_0000203

NP57253.RAe0zZ4LtV8J7tc4Rp0WydL7RdOukxGy-QMW39WUUyuCw
has assertion: NP57253.RAe0zZ4LtV8J7tc4Rp0WydL7RdOukxGy-QMW39WUUyuCw130 assertion
has provenance: NP57253.RAe0zZ4LtV8J7tc4Rp0WydL7RdOukxGy-QMW39WUUyuCw130 provenance
has publication info: NP57253.RAe0zZ4LtV8J7tc4Rp0WydL7RdOukxGy-QMW39WUUyuCw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:26+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57253.RAe0zZ4LtV8J7tc4Rp0WydL7RdOukxGy-QMW39WUUyuCw130 assertion
type: Assertion
description: [To determine whether 5-hydroxytryptamine 2C (5-HT2C) receptor gene 759C/T polymorphism influences the weight gain following antipsychotic agents (APS) treatment in patient with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12425817
was generated by: ECO_0000203

NP57262.RAewgb790tqLpjEf8SiKOHmU7dMcPkL7cHtt3e5YeuwOE
has assertion: NP57262.RAewgb790tqLpjEf8SiKOHmU7dMcPkL7cHtt3e5YeuwOE130 assertion
has provenance: NP57262.RAewgb790tqLpjEf8SiKOHmU7dMcPkL7cHtt3e5YeuwOE130 provenance
has publication info: NP57262.RAewgb790tqLpjEf8SiKOHmU7dMcPkL7cHtt3e5YeuwOE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57262.RAewgb790tqLpjEf8SiKOHmU7dMcPkL7cHtt3e5YeuwOE130 assertion
type: Assertion
description: [A haplotype analyses between the (GT)12-18/(CT)4-5 motif and a Cys23Ser variant of the 5-HT2C gene (which had previously been genotyped in the same sample) showed similar distributions between cases and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11502363
was generated by: ECO_0000203

NP57264.RAe-mwnDD3L-Pj82EQymKDlnoL5YeM8Li3tH9DwKaAXQM
has assertion: NP57264.RAe-mwnDD3L-Pj82EQymKDlnoL5YeM8Li3tH9DwKaAXQM130 assertion
has provenance: NP57264.RAe-mwnDD3L-Pj82EQymKDlnoL5YeM8Li3tH9DwKaAXQM130 provenance
has publication info: NP57264.RAe-mwnDD3L-Pj82EQymKDlnoL5YeM8Li3tH9DwKaAXQM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57264.RAe-mwnDD3L-Pj82EQymKDlnoL5YeM8Li3tH9DwKaAXQM130 assertion
type: Assertion
description: [Association studies of 5-HT2A and 5-HT2C serotonin receptor gene polymorphisms with prophylactic lithium response in bipolar patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16382194
was generated by: ECO_0000203

NP57266.RAZtxwp4IBq9sgbSg4gLN75m8KmzqcFUmEMyxff9R1kXc
has assertion: NP57266.RAZtxwp4IBq9sgbSg4gLN75m8KmzqcFUmEMyxff9R1kXc130 assertion
has provenance: NP57266.RAZtxwp4IBq9sgbSg4gLN75m8KmzqcFUmEMyxff9R1kXc130 provenance
has publication info: NP57266.RAZtxwp4IBq9sgbSg4gLN75m8KmzqcFUmEMyxff9R1kXc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57266.RAZtxwp4IBq9sgbSg4gLN75m8KmzqcFUmEMyxff9R1kXc130 assertion
type: Assertion
description: [the results indicate a possible association between 5HT2C and alcohol use disorder comorbidity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20071033
was generated by: ECO_0000203

NP57269.RAXrZca5k8rgQiFZBoI6MYJL49VGutRcyquxlSTes0L0A
has assertion: NP57269.RAXrZca5k8rgQiFZBoI6MYJL49VGutRcyquxlSTes0L0A130 assertion
has provenance: NP57269.RAXrZca5k8rgQiFZBoI6MYJL49VGutRcyquxlSTes0L0A130 provenance
has publication info: NP57269.RAXrZca5k8rgQiFZBoI6MYJL49VGutRcyquxlSTes0L0A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57269.RAXrZca5k8rgQiFZBoI6MYJL49VGutRcyquxlSTes0L0A130 assertion
type: Assertion
description: [A haplotype analyses between the (GT)12-18/(CT)4-5 motif and a Cys23Ser variant of the 5-HT2C gene (which had previously been genotyped in the same sample) showed similar distributions between cases and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11502363
was generated by: ECO_0000203

NP57276.RATaKh7UU8I7crNVKBSKXLkIJCKiZdhopHWAGvxffB i4
has assertion: NP57276.RATaKh7UU8I7crNVKBSKXLkIJCKiZdhopHWAGvxffB i4130 assertion
has provenance: NP57276.RATaKh7UU8I7crNVKBSKXLkIJCKiZdhopHWAGvxffB i4130 provenance
has publication info: NP57276.RATaKh7UU8I7crNVKBSKXLkIJCKiZdhopHWAGvxffB i4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57276.RATaKh7UU8I7crNVKBSKXLkIJCKiZdhopHWAGvxffB i4130 assertion
type: Assertion
description: [We conclude that sequence variation in the BACE1 or BACE 2 gene is not a significant risk factor for AD; however, a combination of a specific BACE1 allele and APOE varepsilon 4 may increase the risk for Alzheimer disease over and above that attributed to APOE varepsilon 4 alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12707936
was generated by: ECO_0000203

NP57277.RAfl7ree1Y9tzzH kdQdGaYJT7ub VjPDfsDFqWA-wXOY
has assertion: NP57277.RAfl7ree1Y9tzzH kdQdGaYJT7ub VjPDfsDFqWA-wXOY130 assertion
has provenance: NP57277.RAfl7ree1Y9tzzH kdQdGaYJT7ub VjPDfsDFqWA-wXOY130 provenance
has publication info: NP57277.RAfl7ree1Y9tzzH kdQdGaYJT7ub VjPDfsDFqWA-wXOY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57277.RAfl7ree1Y9tzzH kdQdGaYJT7ub VjPDfsDFqWA-wXOY130 assertion
type: Assertion
description: [Our data extend the evidence that HTR2C promoter variation may be a risk factor for obesity and, perhaps through heterosis, influences weight loss by obese women. Pharmacogenetic testing of HTR2C promoter variants may be valuable when evaluating anti-obesity drugs which act directly or indirectly on the receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15048662
was generated by: ECO_0000203

NP57287.RASZzrmMRFVURLfat1Fm5IEUVweCHGSeo6772KeC5c0WU
has assertion: NP57287.RASZzrmMRFVURLfat1Fm5IEUVweCHGSeo6772KeC5c0WU130 assertion
has provenance: NP57287.RASZzrmMRFVURLfat1Fm5IEUVweCHGSeo6772KeC5c0WU130 provenance
has publication info: NP57287.RASZzrmMRFVURLfat1Fm5IEUVweCHGSeo6772KeC5c0WU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57287.RASZzrmMRFVURLfat1Fm5IEUVweCHGSeo6772KeC5c0WU130 assertion
type: Assertion
description: [Genes involved in the transmission, reuptake and metabolism of serotonin constitute a set of candidate genes that could be involved in core aspects of alcoholism, such as the tendency to prefer immediate reward, despite negative consequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15581469
was generated by: ECO_0000203

NP57288.RAZ5FCFsXnAe4ttmzRbSUN8fVJ4xU1A57xtI3aIB1ZBrk
has assertion: NP57288.RAZ5FCFsXnAe4ttmzRbSUN8fVJ4xU1A57xtI3aIB1ZBrk130 assertion
has provenance: NP57288.RAZ5FCFsXnAe4ttmzRbSUN8fVJ4xU1A57xtI3aIB1ZBrk130 provenance
has publication info: NP57288.RAZ5FCFsXnAe4ttmzRbSUN8fVJ4xU1A57xtI3aIB1ZBrk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57288.RAZ5FCFsXnAe4ttmzRbSUN8fVJ4xU1A57xtI3aIB1ZBrk130 assertion
type: Assertion
description: [The clinical and socio-demographic characteristics were not significantly different between the two groups; the genetic analysis revealed a significant correlation between the C/C genotype of 5-HT2A and TD (p=0.017).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15383158
was generated by: ECO_0000203

NP57289.RAROoTTgaNrX6Wr4wSfQuO1WLV5PTQd8dKuP0qAbXQI00
has assertion: NP57289.RAROoTTgaNrX6Wr4wSfQuO1WLV5PTQd8dKuP0qAbXQI00130 assertion
has provenance: NP57289.RAROoTTgaNrX6Wr4wSfQuO1WLV5PTQd8dKuP0qAbXQI00130 provenance
has publication info: NP57289.RAROoTTgaNrX6Wr4wSfQuO1WLV5PTQd8dKuP0qAbXQI00130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57289.RAROoTTgaNrX6Wr4wSfQuO1WLV5PTQd8dKuP0qAbXQI00130 assertion
type: Assertion
description: [The objective of this study was to determine association of T102C and His452Tyr polymorphisms in the 5-HT(2A) receptor gene (HTR(2A)) with TD in a large, multicentre patient sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15857569
was generated by: ECO_0000203

NP57304.RAUU2R5ganes8Otfj1QCjo5nTFCA1Su6euQZm978My7QY
has assertion: NP57304.RAUU2R5ganes8Otfj1QCjo5nTFCA1Su6euQZm978My7QY130 assertion
has provenance: NP57304.RAUU2R5ganes8Otfj1QCjo5nTFCA1Su6euQZm978My7QY130 provenance
has publication info: NP57304.RAUU2R5ganes8Otfj1QCjo5nTFCA1Su6euQZm978My7QY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57304.RAUU2R5ganes8Otfj1QCjo5nTFCA1Su6euQZm978My7QY130 assertion
type: Assertion
description: [The results of this study suggest that response in venlafaxine-treated OCD patients is associated with the S/L genotype of the 5-HTTLPR polymorphism and in paroxetine-treated OCD patients with the G/G genotype of the 5-HT2A polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17503984
was generated by: ECO_0000203

NP57308.RAQDimrbv ZdwIQanBM7h0wnvg1TBjIqqLjdQ97iJdIzY
has assertion: NP57308.RAQDimrbv ZdwIQanBM7h0wnvg1TBjIqqLjdQ97iJdIzY130 assertion
has provenance: NP57308.RAQDimrbv ZdwIQanBM7h0wnvg1TBjIqqLjdQ97iJdIzY130 provenance
has publication info: NP57308.RAQDimrbv ZdwIQanBM7h0wnvg1TBjIqqLjdQ97iJdIzY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57308.RAQDimrbv ZdwIQanBM7h0wnvg1TBjIqqLjdQ97iJdIzY130 assertion
type: Assertion
description: [Therefore, we conducted a case-control study with Japanese samples (738 schizophrenia patients, 196 methamphetamine-induced psychosis patients, and 802 controls) to evaluate the association and interaction between GRM2, HTR2A and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20211215
was generated by: ECO_0000203

NP57309.RAQHgfCPFum3OzJQ7Eza6HCoQW8rpm7KF3HPFz9K8-HE8
has assertion: NP57309.RAQHgfCPFum3OzJQ7Eza6HCoQW8rpm7KF3HPFz9K8-HE8130 assertion
has provenance: NP57309.RAQHgfCPFum3OzJQ7Eza6HCoQW8rpm7KF3HPFz9K8-HE8130 provenance
has publication info: NP57309.RAQHgfCPFum3OzJQ7Eza6HCoQW8rpm7KF3HPFz9K8-HE8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57309.RAQHgfCPFum3OzJQ7Eza6HCoQW8rpm7KF3HPFz9K8-HE8130 assertion
type: Assertion
description: [We conducted a pharmacogenetic study to evaluate whether variants in dopamine-related genes (DRD1-DRD5, AKT1 and GSK3beta) and serotonin receptor genes (HTR1A, HTR1B, HTR1D, HTR2A, HTR2C, HTR6 and HTR7) can be used to predict the efficacy of risperidone treatment for schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18855532
was generated by: ECO_0000203

NP57310.RAaKM9BcspuU8SeK57QTeNK3W7xW9yhPO-Om9c3NUmOZc
has assertion: NP57310.RAaKM9BcspuU8SeK57QTeNK3W7xW9yhPO-Om9c3NUmOZc130 assertion
has provenance: NP57310.RAaKM9BcspuU8SeK57QTeNK3W7xW9yhPO-Om9c3NUmOZc130 provenance
has publication info: NP57310.RAaKM9BcspuU8SeK57QTeNK3W7xW9yhPO-Om9c3NUmOZc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57310.RAaKM9BcspuU8SeK57QTeNK3W7xW9yhPO-Om9c3NUmOZc130 assertion
type: Assertion
description: [Serotonin receptor (5-HTR2A) and dysbindin (DTNBP1) genes and component process variables of short-term verbal memory in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19672240
was generated by: ECO_0000203

NP57312.RAaXQGLt45XORQRR-YBS2OYil-jc2mUPOTKY8eoUusFDE
has assertion: NP57312.RAaXQGLt45XORQRR-YBS2OYil-jc2mUPOTKY8eoUusFDE130 assertion
has provenance: NP57312.RAaXQGLt45XORQRR-YBS2OYil-jc2mUPOTKY8eoUusFDE130 provenance
has publication info: NP57312.RAaXQGLt45XORQRR-YBS2OYil-jc2mUPOTKY8eoUusFDE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57312.RAaXQGLt45XORQRR-YBS2OYil-jc2mUPOTKY8eoUusFDE130 assertion
type: Assertion
description: [Some studies have suggested that the efficacy of atypical antipsychotics on schizophrenia treatment may be related to the serotonin 2A receptor (5-HT2A), and that serotonergic drugs may induce psychotic symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17420819
was generated by: ECO_0000203

NP57317.RATDlybaMrT5yM9ASKRcFi5hS7l909prmpxjzF75yg2f8
has assertion: NP57317.RATDlybaMrT5yM9ASKRcFi5hS7l909prmpxjzF75yg2f8130 assertion
has provenance: NP57317.RATDlybaMrT5yM9ASKRcFi5hS7l909prmpxjzF75yg2f8130 provenance
has publication info: NP57317.RATDlybaMrT5yM9ASKRcFi5hS7l909prmpxjzF75yg2f8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57317.RATDlybaMrT5yM9ASKRcFi5hS7l909prmpxjzF75yg2f8130 assertion
type: Assertion
description: [Here we report the results from an association candidate-gene approach, where we analyzed 15 single nucleotide polymorphisms (SNPs) within the gene coding for the serotonin-receptor 2A (HTR2A) in patients suffering from PD and a control sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17440930
was generated by: ECO_0000203

NP57318.RAd4ggka7JbmAWORytxuVaErGAhmmXfOcjrGuWyIrBlv8
has assertion: NP57318.RAd4ggka7JbmAWORytxuVaErGAhmmXfOcjrGuWyIrBlv8130 assertion
has provenance: NP57318.RAd4ggka7JbmAWORytxuVaErGAhmmXfOcjrGuWyIrBlv8130 provenance
has publication info: NP57318.RAd4ggka7JbmAWORytxuVaErGAhmmXfOcjrGuWyIrBlv8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57318.RAd4ggka7JbmAWORytxuVaErGAhmmXfOcjrGuWyIrBlv8130 assertion
type: Assertion
description: [Nine gene-candidates, including 5-HTTLPR, MAO-A VNTR, TPH2 rs1386494, 5-HTR1A -1019C-G, 5-HTR2A 102T-C, CCKR1 246G-A, CCKR2 -215C-A, DRD1 -94G-A and COMT Val158Met, were selected for genotyping based on previous positive findings from genetic association studies in PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18832011
was generated by: ECO_0000203

NP57319.RAVSPgqLWegefXN8582 GgzZtKJKZ-PSTWMgNC6v1hcFM
has assertion: NP57319.RAVSPgqLWegefXN8582 GgzZtKJKZ-PSTWMgNC6v1hcFM130 assertion
has provenance: NP57319.RAVSPgqLWegefXN8582 GgzZtKJKZ-PSTWMgNC6v1hcFM130 provenance
has publication info: NP57319.RAVSPgqLWegefXN8582 GgzZtKJKZ-PSTWMgNC6v1hcFM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57319.RAVSPgqLWegefXN8582 GgzZtKJKZ-PSTWMgNC6v1hcFM130 assertion
type: Assertion
description: [This study reinforces the association between HTR1A and PD. No major evidence of gene-environment interaction in PD with parenting or trauma was found. Further studies are necessary in order to confirm these findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20817074
was generated by: ECO_0000203

NP57326.RAXBS13oqO6uRNKw1lJY wbapT91Xt0QzFvzx7Ku-T7nI
has assertion: NP57326.RAXBS13oqO6uRNKw1lJY wbapT91Xt0QzFvzx7Ku-T7nI130 assertion
has provenance: NP57326.RAXBS13oqO6uRNKw1lJY wbapT91Xt0QzFvzx7Ku-T7nI130 provenance
has publication info: NP57326.RAXBS13oqO6uRNKw1lJY wbapT91Xt0QzFvzx7Ku-T7nI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57326.RAXBS13oqO6uRNKw1lJY wbapT91Xt0QzFvzx7Ku-T7nI130 assertion
type: Assertion
description: [Thus, the polymorphic alleles of SHTR2A proved to be associated with personality traits in mentally healthy people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15285608
was generated by: ECO_0000203

NP57330.RATeaCpPEH1aVnFusIHEUwg6Fyu Syqs460GbvY4rJtn0
has assertion: NP57330.RATeaCpPEH1aVnFusIHEUwg6Fyu Syqs460GbvY4rJtn0130 assertion
has provenance: NP57330.RATeaCpPEH1aVnFusIHEUwg6Fyu Syqs460GbvY4rJtn0130 provenance
has publication info: NP57330.RATeaCpPEH1aVnFusIHEUwg6Fyu Syqs460GbvY4rJtn0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57330.RATeaCpPEH1aVnFusIHEUwg6Fyu Syqs460GbvY4rJtn0130 assertion
type: Assertion
description: [5-HTR1A, 5-HTR2A, 5-HTR6, TPH1 and TPH2 polymorphisms and major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19590397
was generated by: ECO_0000203

NP57332.RAXhuBP42JaHJZDHtPZylJUXUyw8vQ5duQg-SSYPLKd2Y
has assertion: NP57332.RAXhuBP42JaHJZDHtPZylJUXUyw8vQ5duQg-SSYPLKd2Y130 assertion
has provenance: NP57332.RAXhuBP42JaHJZDHtPZylJUXUyw8vQ5duQg-SSYPLKd2Y130 provenance
has publication info: NP57332.RAXhuBP42JaHJZDHtPZylJUXUyw8vQ5duQg-SSYPLKd2Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57332.RAXhuBP42JaHJZDHtPZylJUXUyw8vQ5duQg-SSYPLKd2Y130 assertion
type: Assertion
description: [A suggestive association of sequence variations in genes responsible for the synthesis (TPH), recognition (5-HTR2A), and degradation (MAOA) of serotonin with depression symptomatology was found, although the effect was generally restricted to men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16806099
was generated by: ECO_0000203

NP57339.RAXgFDEkCHtUzzmXEx 1Sty5tza4S2-86-R5W-LWxm4Tw
has assertion: NP57339.RAXgFDEkCHtUzzmXEx 1Sty5tza4S2-86-R5W-LWxm4Tw130 assertion
has provenance: NP57339.RAXgFDEkCHtUzzmXEx 1Sty5tza4S2-86-R5W-LWxm4Tw130 provenance
has publication info: NP57339.RAXgFDEkCHtUzzmXEx 1Sty5tza4S2-86-R5W-LWxm4Tw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57339.RAXgFDEkCHtUzzmXEx 1Sty5tza4S2-86-R5W-LWxm4Tw130 assertion
type: Assertion
description: [The aim of the present study was to test for possible associations between the A-1438G polymorphism in the serotonin receptor gene (HTR2A) with tobacco smoking combined or not with alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19111403
was generated by: ECO_0000203

NP57344.RAZNHsJssIaNPpbB-d0FH9uNn17vtn7zJehO6r7QFcyI8
has assertion: NP57344.RAZNHsJssIaNPpbB-d0FH9uNn17vtn7zJehO6r7QFcyI8130 assertion
has provenance: NP57344.RAZNHsJssIaNPpbB-d0FH9uNn17vtn7zJehO6r7QFcyI8130 provenance
has publication info: NP57344.RAZNHsJssIaNPpbB-d0FH9uNn17vtn7zJehO6r7QFcyI8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57344.RAZNHsJssIaNPpbB-d0FH9uNn17vtn7zJehO6r7QFcyI8130 assertion
type: Assertion
description: [Thus, although our findings cannot specifically refute the hypothesis of Du et al. that genetic variation in the 5-HT2A receptor gene is associated with increased vulnerability to suicidal ideation in those with major depression, they certainly do not support the more important hypothesis that such a genetic variation is associated with completed suicide itself.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11121203
was generated by: ECO_0000203

NP57357.RAfjjdjMysVPnOtPW9cVfwtJCDiniL6wFgs8pVIyvAzuE
has assertion: NP57357.RAfjjdjMysVPnOtPW9cVfwtJCDiniL6wFgs8pVIyvAzuE130 assertion
has provenance: NP57357.RAfjjdjMysVPnOtPW9cVfwtJCDiniL6wFgs8pVIyvAzuE130 provenance
has publication info: NP57357.RAfjjdjMysVPnOtPW9cVfwtJCDiniL6wFgs8pVIyvAzuE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57357.RAfjjdjMysVPnOtPW9cVfwtJCDiniL6wFgs8pVIyvAzuE130 assertion
type: Assertion
description: [Delusion symptoms and response to antipsychotic treatment are associated with the 5-HT2A receptor polymorphism (102T/C) in Alzheimer's disease: a 3-year follow-up longitudinal study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19494443
was generated by: ECO_0000203

NP57367.RAS-dK1oVqWz6fNrsSsPs4oY jfpI1bUpqVlkhbaYHFVo
has assertion: NP57367.RAS-dK1oVqWz6fNrsSsPs4oY jfpI1bUpqVlkhbaYHFVo130 assertion
has provenance: NP57367.RAS-dK1oVqWz6fNrsSsPs4oY jfpI1bUpqVlkhbaYHFVo130 provenance
has publication info: NP57367.RAS-dK1oVqWz6fNrsSsPs4oY jfpI1bUpqVlkhbaYHFVo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57367.RAS-dK1oVqWz6fNrsSsPs4oY jfpI1bUpqVlkhbaYHFVo130 assertion
type: Assertion
description: [Association studies of 5-HT2A and 5-HT2C serotonin receptor gene polymorphisms with prophylactic lithium response in bipolar patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16382194
was generated by: ECO_0000203

NP57369.RAQ07Fv2zySRzQgxsJZZveGiJO99vY9Q dDkNpw8-hHRU
has assertion: NP57369.RAQ07Fv2zySRzQgxsJZZveGiJO99vY9Q dDkNpw8-hHRU130 assertion
has provenance: NP57369.RAQ07Fv2zySRzQgxsJZZveGiJO99vY9Q dDkNpw8-hHRU130 provenance
has publication info: NP57369.RAQ07Fv2zySRzQgxsJZZveGiJO99vY9Q dDkNpw8-hHRU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57369.RAQ07Fv2zySRzQgxsJZZveGiJO99vY9Q dDkNpw8-hHRU130 assertion
type: Assertion
description: [ The association detected in this study suggests that the 5-HT(2A) receptor gene may play a role in the genetic susceptibility to bipolar disorder, through a specific subgroup of bipolar type I patients with lower risk of suicidal behavior.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11983190
was generated by: ECO_0000203

NP57374.RAUWpue448njvESb8cAPE9fmjvq4wJ-qoOhurkUQIGBRA
has assertion: NP57374.RAUWpue448njvESb8cAPE9fmjvq4wJ-qoOhurkUQIGBRA130 assertion
has provenance: NP57374.RAUWpue448njvESb8cAPE9fmjvq4wJ-qoOhurkUQIGBRA130 provenance
has publication info: NP57374.RAUWpue448njvESb8cAPE9fmjvq4wJ-qoOhurkUQIGBRA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57374.RAUWpue448njvESb8cAPE9fmjvq4wJ-qoOhurkUQIGBRA130 assertion
type: Assertion
description: [Hyperserotonemia in autism: the potential role of 5HT-related gene variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18405062
was generated by: ECO_0000203

NP57376.RAcqyuzXOSUI27gEXG6yohyDh51-T9UBTBPFWIQcc3UZQ
has assertion: NP57376.RAcqyuzXOSUI27gEXG6yohyDh51-T9UBTBPFWIQcc3UZQ130 assertion
has provenance: NP57376.RAcqyuzXOSUI27gEXG6yohyDh51-T9UBTBPFWIQcc3UZQ130 provenance
has publication info: NP57376.RAcqyuzXOSUI27gEXG6yohyDh51-T9UBTBPFWIQcc3UZQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57376.RAcqyuzXOSUI27gEXG6yohyDh51-T9UBTBPFWIQcc3UZQ130 assertion
type: Assertion
description: [Analysis of serotonin receptor 2A gene (HTR2A): association study with autism spectrum disorder in the Indian population and investigation of the gene expression in peripheral blood leukocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19647026
was generated by: ECO_0000203

NP57378.RAfZ1fX2A0qhaw-nM7dw5nu3xKd7GoTcJ mkTLCeYKQEI
has assertion: NP57378.RAfZ1fX2A0qhaw-nM7dw5nu3xKd7GoTcJ mkTLCeYKQEI130 assertion
has provenance: NP57378.RAfZ1fX2A0qhaw-nM7dw5nu3xKd7GoTcJ mkTLCeYKQEI130 provenance
has publication info: NP57378.RAfZ1fX2A0qhaw-nM7dw5nu3xKd7GoTcJ mkTLCeYKQEI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57378.RAfZ1fX2A0qhaw-nM7dw5nu3xKd7GoTcJ mkTLCeYKQEI130 assertion
type: Assertion
description: [To determine the influence of genetic variation at the 5-HT(2A) receptor (T102C polymorphism) and the 5-HTT (insertion/deletion polymorphism) on the risk of developing early MI, we genotyped 210 MI patients of < 55 years old and 238 healthy control subjects for DNA polymorphisms in these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12605580
was generated by: ECO_0000203

NP57389.RAbZJuE10WIQ2vE1JuCXe78UL52Qp-7Lf -gxbdph2lek
has assertion: NP57389.RAbZJuE10WIQ2vE1JuCXe78UL52Qp-7Lf -gxbdph2lek130 assertion
has provenance: NP57389.RAbZJuE10WIQ2vE1JuCXe78UL52Qp-7Lf -gxbdph2lek130 provenance
has publication info: NP57389.RAbZJuE10WIQ2vE1JuCXe78UL52Qp-7Lf -gxbdph2lek130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57389.RAbZJuE10WIQ2vE1JuCXe78UL52Qp-7Lf -gxbdph2lek130 assertion
type: Assertion
description: [Fine mapping of the human 5-HTR2a gene to chromosome 13q14 and identification of two highly polymorphic linked markers suitable for association studies in psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10464662
was generated by: ECO_0000203

NP57391.RASg9rlucLen2Z0cSlm6NPAOx U lVKv5vGI7xWOoqkgk
has assertion: NP57391.RASg9rlucLen2Z0cSlm6NPAOx U lVKv5vGI7xWOoqkgk130 assertion
has provenance: NP57391.RASg9rlucLen2Z0cSlm6NPAOx U lVKv5vGI7xWOoqkgk130 provenance
has publication info: NP57391.RASg9rlucLen2Z0cSlm6NPAOx U lVKv5vGI7xWOoqkgk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57391.RASg9rlucLen2Z0cSlm6NPAOx U lVKv5vGI7xWOoqkgk130 assertion
type: Assertion
description: [Although no statistically significant genotypic or allelic associations were detected, the data yielded interesting preliminary results that warrant further discussion and investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12650952
was generated by: ECO_0000203

NP57395.RAURxisYEw CehYmDBOYe-ZDyr7R2Wq qjOCBIiI5kBZY
has assertion: NP57395.RAURxisYEw CehYmDBOYe-ZDyr7R2Wq qjOCBIiI5kBZY130 assertion
has provenance: NP57395.RAURxisYEw CehYmDBOYe-ZDyr7R2Wq qjOCBIiI5kBZY130 provenance
has publication info: NP57395.RAURxisYEw CehYmDBOYe-ZDyr7R2Wq qjOCBIiI5kBZY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57395.RAURxisYEw CehYmDBOYe-ZDyr7R2Wq qjOCBIiI5kBZY130 assertion
type: Assertion
description: [A family-based association study of the 5-HT-1Dbeta receptor gene in obsessive-compulsive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14731309
was generated by: ECO_0000203

NP57397.RAUbeOniurjIzz 5IpVjYB2V1ljR dIO6Am4Vj9TJsyQ8
has assertion: NP57397.RAUbeOniurjIzz 5IpVjYB2V1ljR dIO6Am4Vj9TJsyQ8130 assertion
has provenance: NP57397.RAUbeOniurjIzz 5IpVjYB2V1ljR dIO6Am4Vj9TJsyQ8130 provenance
has publication info: NP57397.RAUbeOniurjIzz 5IpVjYB2V1ljR dIO6Am4Vj9TJsyQ8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57397.RAUbeOniurjIzz 5IpVjYB2V1ljR dIO6Am4Vj9TJsyQ8130 assertion
type: Assertion
description: [Association of a 5-HT1Dbeta receptor gene polymorphism with obsessive-compulsive disorder in Korean male subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19325252
was generated by: ECO_0000203

NP57400.RAR8971XP7e5n5mVFMOzetQaNKfROKgyRKoLfv33wi6lM
has assertion: NP57400.RAR8971XP7e5n5mVFMOzetQaNKfROKgyRKoLfv33wi6lM130 assertion
has provenance: NP57400.RAR8971XP7e5n5mVFMOzetQaNKfROKgyRKoLfv33wi6lM130 provenance
has publication info: NP57400.RAR8971XP7e5n5mVFMOzetQaNKfROKgyRKoLfv33wi6lM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57400.RAR8971XP7e5n5mVFMOzetQaNKfROKgyRKoLfv33wi6lM130 assertion
type: Assertion
description: [Taken together with recent observations, these results suggest that genetic variability of the 5HT1B receptor is involved in the development of some type of alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11956970
was generated by: ECO_0000203

NP57403.RAcm7kd9GzhvSvbnb0ZadVht0PLykqoQl9lOL6YdYnso0
has assertion: NP57403.RAcm7kd9GzhvSvbnb0ZadVht0PLykqoQl9lOL6YdYnso0130 assertion
has provenance: NP57403.RAcm7kd9GzhvSvbnb0ZadVht0PLykqoQl9lOL6YdYnso0130 provenance
has publication info: NP57403.RAcm7kd9GzhvSvbnb0ZadVht0PLykqoQl9lOL6YdYnso0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57403.RAcm7kd9GzhvSvbnb0ZadVht0PLykqoQl9lOL6YdYnso0130 assertion
type: Assertion
description: [These findings indicate that genetic variants conceivably related to lower 5-HT neurotransmission may be involved in the development of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15670397
was generated by: ECO_0000203

NP57412.RAWXoOKYBcbRSC-3VMkiPXTMwu9NyxQ9odkgcQQBTKix4
has assertion: NP57412.RAWXoOKYBcbRSC-3VMkiPXTMwu9NyxQ9odkgcQQBTKix4130 assertion
has provenance: NP57412.RAWXoOKYBcbRSC-3VMkiPXTMwu9NyxQ9odkgcQQBTKix4130 provenance
has publication info: NP57412.RAWXoOKYBcbRSC-3VMkiPXTMwu9NyxQ9odkgcQQBTKix4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57412.RAWXoOKYBcbRSC-3VMkiPXTMwu9NyxQ9odkgcQQBTKix4130 assertion
type: Assertion
description: [Variation in catechol-O-methyltransferase is associated with duloxetine response in a clinical trial for major depressive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19095219
was generated by: ECO_0000203

NP57426.RAWW3bKg1OnH4pErQi1YL9x2OSq4s3v1CmbSA-4ifEsa4
has assertion: NP57426.RAWW3bKg1OnH4pErQi1YL9x2OSq4s3v1CmbSA-4ifEsa4130 assertion
has provenance: NP57426.RAWW3bKg1OnH4pErQi1YL9x2OSq4s3v1CmbSA-4ifEsa4130 provenance
has publication info: NP57426.RAWW3bKg1OnH4pErQi1YL9x2OSq4s3v1CmbSA-4ifEsa4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57426.RAWW3bKg1OnH4pErQi1YL9x2OSq4s3v1CmbSA-4ifEsa4130 assertion
type: Assertion
description: [This is the first possible interaction of genetic variations in panic disorder that has been observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16538182
was generated by: ECO_0000203

NP57438.RAaLL04CLLJZjnhtU8oQgL1TOB5lVADcPvIKCC3gJg-o8
has assertion: NP57438.RAaLL04CLLJZjnhtU8oQgL1TOB5lVADcPvIKCC3gJg-o8130 assertion
has provenance: NP57438.RAaLL04CLLJZjnhtU8oQgL1TOB5lVADcPvIKCC3gJg-o8130 provenance
has publication info: NP57438.RAaLL04CLLJZjnhtU8oQgL1TOB5lVADcPvIKCC3gJg-o8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57438.RAaLL04CLLJZjnhtU8oQgL1TOB5lVADcPvIKCC3gJg-o8130 assertion
type: Assertion
description: [The 5-HT1A receptor gene is repressed by NUDR/DEAF-1 in raphe cells at the C-, but not at the G-allele of the C(-1019)G polymorphism that is associated with major depression and suicide.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15447813
was generated by: ECO_0000203

NP57440.RAaufTVgO lJJPf2Z9xtY5NY0oLbjzJt1zsYQevjm-Uzg
has assertion: NP57440.RAaufTVgO lJJPf2Z9xtY5NY0oLbjzJt1zsYQevjm-Uzg130 assertion
has provenance: NP57440.RAaufTVgO lJJPf2Z9xtY5NY0oLbjzJt1zsYQevjm-Uzg130 provenance
has publication info: NP57440.RAaufTVgO lJJPf2Z9xtY5NY0oLbjzJt1zsYQevjm-Uzg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57440.RAaufTVgO lJJPf2Z9xtY5NY0oLbjzJt1zsYQevjm-Uzg130 assertion
type: Assertion
description: [Our data provided no evidence of association between schizophrenia and the variants in the 5' untranslated region as well as the coding region of the human 5-HT1A receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9754630
was generated by: ECO_0000203

NP57446.RAe7wX oTiFwFyBV YNgoS2Jt4jzQZr0E0JNBkg0UySt4
has assertion: NP57446.RAe7wX oTiFwFyBV YNgoS2Jt4jzQZr0E0JNBkg0UySt4130 assertion
has provenance: NP57446.RAe7wX oTiFwFyBV YNgoS2Jt4jzQZr0E0JNBkg0UySt4130 provenance
has publication info: NP57446.RAe7wX oTiFwFyBV YNgoS2Jt4jzQZr0E0JNBkg0UySt4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57446.RAe7wX oTiFwFyBV YNgoS2Jt4jzQZr0E0JNBkg0UySt4130 assertion
type: Assertion
description: [Association evaluation by Fisher's exact test (p < 0.01) revealed statistically significant SNPs in multiple genes, not only in inflammatory mediators (IL6ST and PTGDS, associated with aggressive periodontitis; and CTSD, associated with severe chronic periodontitis), but also in structural factors of periodontal tissues (COL4A1, COL1A1, and KRT23, associated with aggressive periodontitis; and HSPG2, COL17A1, and EGF, associated with severe chronic periodontitis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15081423
was generated by: ECO_0000203

NP57455.RATqQ4jhxAeVGsVM2gBO7buGa36qBOSpsvcauovoz0CV4
has assertion: NP57455.RATqQ4jhxAeVGsVM2gBO7buGa36qBOSpsvcauovoz0CV4130 assertion
has provenance: NP57455.RATqQ4jhxAeVGsVM2gBO7buGa36qBOSpsvcauovoz0CV4130 provenance
has publication info: NP57455.RATqQ4jhxAeVGsVM2gBO7buGa36qBOSpsvcauovoz0CV4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57455.RATqQ4jhxAeVGsVM2gBO7buGa36qBOSpsvcauovoz0CV4130 assertion
type: Assertion
description: [ Our data show that the bi-allelic NcoI and PstI polymorphisms within the HSP70-HOM and HSP70-2 locus, respectively, are associated with neither susceptibility to nor outcome of severe sepsis. Moreover, we found a linkage between HSP70-2 A homozygotes and the previously reported and mortality-related homozygous genotype, TNFB2/B2, in patients suffering from severe sepsis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10446818
was generated by: ECO_0000203

NP57457.RAZ5ZGUgHxO7Gi9dV6QeT8-3C83 nR0pUiUHaBk66PJhA
has assertion: NP57457.RAZ5ZGUgHxO7Gi9dV6QeT8-3C83 nR0pUiUHaBk66PJhA130 assertion
has provenance: NP57457.RAZ5ZGUgHxO7Gi9dV6QeT8-3C83 nR0pUiUHaBk66PJhA130 provenance
has publication info: NP57457.RAZ5ZGUgHxO7Gi9dV6QeT8-3C83 nR0pUiUHaBk66PJhA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57457.RAZ5ZGUgHxO7Gi9dV6QeT8-3C83 nR0pUiUHaBk66PJhA130 assertion
type: Assertion
description: [Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12082592
was generated by: ECO_0000203

NP57466.RAUkj6JXlHcYWs0ybTiac1aUI4iZoHcJNYQAY3J 6OEI4
has assertion: NP57466.RAUkj6JXlHcYWs0ybTiac1aUI4iZoHcJNYQAY3J 6OEI4130 assertion
has provenance: NP57466.RAUkj6JXlHcYWs0ybTiac1aUI4iZoHcJNYQAY3J 6OEI4130 provenance
has publication info: NP57466.RAUkj6JXlHcYWs0ybTiac1aUI4iZoHcJNYQAY3J 6OEI4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57466.RAUkj6JXlHcYWs0ybTiac1aUI4iZoHcJNYQAY3J 6OEI4130 assertion
type: Assertion
description: [Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12082592
was generated by: ECO_0000203

NP57468.RAexeWmmrxyZe9ORwBVvFaktEiutfQbdY1BXrkfxP93rw
has assertion: NP57468.RAexeWmmrxyZe9ORwBVvFaktEiutfQbdY1BXrkfxP93rw130 assertion
has provenance: NP57468.RAexeWmmrxyZe9ORwBVvFaktEiutfQbdY1BXrkfxP93rw130 provenance
has publication info: NP57468.RAexeWmmrxyZe9ORwBVvFaktEiutfQbdY1BXrkfxP93rw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57468.RAexeWmmrxyZe9ORwBVvFaktEiutfQbdY1BXrkfxP93rw130 assertion
type: Assertion
description: [Polymorphisms of heat shock protein 70 gene (HSPA1A, HSPA1B and HSPA1L) and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15963589
was generated by: ECO_0000203

NP57469.RAR4T2a3WknxL47 d9G G9aNQYjy1kLmP0uud0zXfnfbA
has assertion: NP57469.RAR4T2a3WknxL47 d9G G9aNQYjy1kLmP0uud0zXfnfbA130 assertion
has provenance: NP57469.RAR4T2a3WknxL47 d9G G9aNQYjy1kLmP0uud0zXfnfbA130 provenance
has publication info: NP57469.RAR4T2a3WknxL47 d9G G9aNQYjy1kLmP0uud0zXfnfbA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57469.RAR4T2a3WknxL47 d9G G9aNQYjy1kLmP0uud0zXfnfbA130 assertion
type: Assertion
description: [We previously investigated a group of single-nucleotide polymorphisms of a set of genes coding for heat shock proteins (HSPA1A, HSPA1B and HSPA1L) and found a significant association between one HSPA1B variation and schizophrenia (SZ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19439993
was generated by: ECO_0000203

NP57475.RAbGh0EnZG8DpBbfV043qZLIYL1yWXO1PBujGhWCswACc
has assertion: NP57475.RAbGh0EnZG8DpBbfV043qZLIYL1yWXO1PBujGhWCswACc130 assertion
has provenance: NP57475.RAbGh0EnZG8DpBbfV043qZLIYL1yWXO1PBujGhWCswACc130 provenance
has publication info: NP57475.RAbGh0EnZG8DpBbfV043qZLIYL1yWXO1PBujGhWCswACc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57475.RAbGh0EnZG8DpBbfV043qZLIYL1yWXO1PBujGhWCswACc130 assertion
type: Assertion
description: [ There is a significantly increased association of HSP70-2 B/B genotype with the risk of acute mountain sickness. Individuals with HSP70-2 B/B genotype may have weaker adaptive ability than those without this genotype under altitude stress. The results contribute to provide scientific bases for finding these individuals in specified occupational people, ensuring their health and enhancing work efficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15748471
was generated by: ECO_0000203

NP57478.RASKzCPd 1gVprYGVTIsuhF32JqwaUqdzkrh3U7BDKmLk
has assertion: NP57478.RASKzCPd 1gVprYGVTIsuhF32JqwaUqdzkrh3U7BDKmLk130 assertion
has provenance: NP57478.RASKzCPd 1gVprYGVTIsuhF32JqwaUqdzkrh3U7BDKmLk130 provenance
has publication info: NP57478.RASKzCPd 1gVprYGVTIsuhF32JqwaUqdzkrh3U7BDKmLk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57478.RASKzCPd 1gVprYGVTIsuhF32JqwaUqdzkrh3U7BDKmLk130 assertion
type: Assertion
description: [In contrast, a significant relative risk of NPC was found associated with the HSP70-2 homozygous genotype (P2/P2) (OR=2.309; P=0.006).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12691826
was generated by: ECO_0000203

NP57482.RASsjIc-J-TYvBayHoHMUhwJfZqns6uPFVEZLkhKoMrUw
has assertion: NP57482.RASsjIc-J-TYvBayHoHMUhwJfZqns6uPFVEZLkhKoMrUw130 assertion
has provenance: NP57482.RASsjIc-J-TYvBayHoHMUhwJfZqns6uPFVEZLkhKoMrUw130 provenance
has publication info: NP57482.RASsjIc-J-TYvBayHoHMUhwJfZqns6uPFVEZLkhKoMrUw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57482.RASsjIc-J-TYvBayHoHMUhwJfZqns6uPFVEZLkhKoMrUw130 assertion
type: Assertion
description: [We previously investigated a group of single-nucleotide polymorphisms of a set of genes coding for heat shock proteins (HSPA1A, HSPA1B and HSPA1L) and found a significant association between one HSPA1B variation and schizophrenia (SZ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19439993
was generated by: ECO_0000203

NP57484.RAV5bIbs3QbytUpHIjETBYqnfOjEnU-rBvSHk997IAl8Y
has assertion: NP57484.RAV5bIbs3QbytUpHIjETBYqnfOjEnU-rBvSHk997IAl8Y130 assertion
has provenance: NP57484.RAV5bIbs3QbytUpHIjETBYqnfOjEnU-rBvSHk997IAl8Y130 provenance
has publication info: NP57484.RAV5bIbs3QbytUpHIjETBYqnfOjEnU-rBvSHk997IAl8Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57484.RAV5bIbs3QbytUpHIjETBYqnfOjEnU-rBvSHk997IAl8Y130 assertion
type: Assertion
description: [We have investigated the association of polymorphisms -110 A/C, +190 G/C, +1267 A/G, +2074 G/C, and +2437 G/C in the 5' and coding regions of the HSP70-1, HSP70-2, and HSP70-hom genes with the risk of PD by screening DNA samples from 274 PD patients and 183 controls in assays based on the polymerase chain reaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14605873
was generated by: ECO_0000203

NP57486.RAVC4PwT3coe9c1xomXTOMzb0HSfsZtKWsv2K9D0eFnHY
has assertion: NP57486.RAVC4PwT3coe9c1xomXTOMzb0HSfsZtKWsv2K9D0eFnHY130 assertion
has provenance: NP57486.RAVC4PwT3coe9c1xomXTOMzb0HSfsZtKWsv2K9D0eFnHY130 provenance
has publication info: NP57486.RAVC4PwT3coe9c1xomXTOMzb0HSfsZtKWsv2K9D0eFnHY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57486.RAVC4PwT3coe9c1xomXTOMzb0HSfsZtKWsv2K9D0eFnHY130 assertion
type: Assertion
description: [In addition to the association of SpA with HLA-B27, there is a significant association of HSP70-2 and HSP70-hom alleles with SpA in Mexicans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11779758
was generated by: ECO_0000203

NP57489.RAf4VgpNOoIvT0j XjKUf dGlLlKkjB1D4j1tiKu evYc
has assertion: NP57489.RAf4VgpNOoIvT0j XjKUf dGlLlKkjB1D4j1tiKu evYc130 assertion
has provenance: NP57489.RAf4VgpNOoIvT0j XjKUf dGlLlKkjB1D4j1tiKu evYc130 provenance
has publication info: NP57489.RAf4VgpNOoIvT0j XjKUf dGlLlKkjB1D4j1tiKu evYc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57489.RAf4VgpNOoIvT0j XjKUf dGlLlKkjB1D4j1tiKu evYc130 assertion
type: Assertion
description: [Men with the variant genotypes at either B1-N367T or B2-c7519g had a significantly higher risk to develop prostate cancer, especially the hereditary type of prostate cancer. Most importantly, the subset of hereditary prostate cancer probands, whose families provided evidence for linkage at 1p13, predominantly contributed to the observed association. Additional studies are warranted to confirm these findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11912155
was generated by: ECO_0000203

NP57492.RAQMU3WSoiYdKLzN6-ROfartXuqwSAX8w5VQwZ1pPxtxI
has assertion: NP57492.RAQMU3WSoiYdKLzN6-ROfartXuqwSAX8w5VQwZ1pPxtxI130 assertion
has provenance: NP57492.RAQMU3WSoiYdKLzN6-ROfartXuqwSAX8w5VQwZ1pPxtxI130 provenance
has publication info: NP57492.RAQMU3WSoiYdKLzN6-ROfartXuqwSAX8w5VQwZ1pPxtxI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57492.RAQMU3WSoiYdKLzN6-ROfartXuqwSAX8w5VQwZ1pPxtxI130 assertion
type: Assertion
description: [Quantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium (BPC3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19574343
was generated by: ECO_0000203

NP57494.RAdwIHbZNIeHK-di9LWqiz6foeNKmdCAAcW03fmjhxkMY
has assertion: NP57494.RAdwIHbZNIeHK-di9LWqiz6foeNKmdCAAcW03fmjhxkMY130 assertion
has provenance: NP57494.RAdwIHbZNIeHK-di9LWqiz6foeNKmdCAAcW03fmjhxkMY130 provenance
has publication info: NP57494.RAdwIHbZNIeHK-di9LWqiz6foeNKmdCAAcW03fmjhxkMY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57494.RAdwIHbZNIeHK-di9LWqiz6foeNKmdCAAcW03fmjhxkMY130 assertion
type: Assertion
description: [Therefore, our results indicate that the BAT-40 containing region and to a less extend the thyroid hormone receptor-alpha1 gene are related to thyroid cancer susceptibility. To our knowledge, this is the first study reporting the identification of genetic factors for thyroid cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15767343
was generated by: ECO_0000203

NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x K wbULoR8
has assertion: NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x K wbULoR8130 assertion
has provenance: NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x K wbULoR8130 provenance
has publication info: NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x K wbULoR8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x K wbULoR8130 assertion
type: Assertion
description: [Men with the variant genotypes at either B1-N367T or B2-c7519g had a significantly higher risk to develop prostate cancer, especially the hereditary type of prostate cancer. Most importantly, the subset of hereditary prostate cancer probands, whose families provided evidence for linkage at 1p13, predominantly contributed to the observed association. Additional studies are warranted to confirm these findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11912155
was generated by: ECO_0000203

NP57503.RAWq3rqsWafZUGDuYNsZNJrDFpfKvBTlc74UrGPCAiWQ4
has assertion: NP57503.RAWq3rqsWafZUGDuYNsZNJrDFpfKvBTlc74UrGPCAiWQ4130 assertion
has provenance: NP57503.RAWq3rqsWafZUGDuYNsZNJrDFpfKvBTlc74UrGPCAiWQ4130 provenance
has publication info: NP57503.RAWq3rqsWafZUGDuYNsZNJrDFpfKvBTlc74UrGPCAiWQ4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57503.RAWq3rqsWafZUGDuYNsZNJrDFpfKvBTlc74UrGPCAiWQ4130 assertion
type: Assertion
description: [Steroid biosynthesis and renal excretion in human essential hypertension: association with blood pressure and endogenous ouabain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19197249
was generated by: ECO_0000203

NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6 iomRmdanVo22c
has assertion: NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6 iomRmdanVo22c130 assertion
has provenance: NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6 iomRmdanVo22c130 provenance
has publication info: NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6 iomRmdanVo22c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57504.RASFjfKFCEZ2JiH-qXjZcMpgkzAghP6 iomRmdanVo22c130 assertion
type: Assertion
description: [A total of 275 EH patients and 286 controls were genotyped for four SNPs of the HSD3B1 gene (rs3765945, rs3088283, rs6203, and rs1047303) and for two SNPs of the HSD3B2 gene (rs2854964 and rs1819698).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20660004
was generated by: ECO_0000203

NP57506.RARaq9VbWn aliPxwRx NMntnZ5TM9zwkEUti5Z-8Nuc
has assertion: NP57506.RARaq9VbWn aliPxwRx NMntnZ5TM9zwkEUti5Z-8Nuc130 assertion
has provenance: NP57506.RARaq9VbWn aliPxwRx NMntnZ5TM9zwkEUti5Z-8Nuc130 provenance
has publication info: NP57506.RARaq9VbWn aliPxwRx NMntnZ5TM9zwkEUti5Z-8Nuc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57506.RARaq9VbWn aliPxwRx NMntnZ5TM9zwkEUti5Z-8Nuc130 assertion
type: Assertion
description: [The hormonal phenotype of Nonclassic 3 beta-hydroxysteroid dehydrogenase (HSD3B) deficiency in hyperandrogenic females is associated with insulin-resistant polycystic ovary syndrome and is not a variant of inherited HSD3B2 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/14764797
was generated by: ECO_0000203

NP57507.RAQ2P97R-9BBVKygOq32aes41BoXTLSJzFSUPTC9IK4QE
has assertion: NP57507.RAQ2P97R-9BBVKygOq32aes41BoXTLSJzFSUPTC9IK4QE130 assertion
has provenance: NP57507.RAQ2P97R-9BBVKygOq32aes41BoXTLSJzFSUPTC9IK4QE130 provenance
has publication info: NP57507.RAQ2P97R-9BBVKygOq32aes41BoXTLSJzFSUPTC9IK4QE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57507.RAQ2P97R-9BBVKygOq32aes41BoXTLSJzFSUPTC9IK4QE130 assertion
type: Assertion
description: [ Our data are consistent with a plausible role of the G289S SNP in prostate cancer susceptibility. Therefore, the HSD17B3 gene may be a plausible candidate gene for prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12210481
was generated by: ECO_0000203

NP57510.RAcColOyJUX87Mo3rBCNHTBsOeQjNjS8YZIkCIw4i s44
has assertion: NP57510.RAcColOyJUX87Mo3rBCNHTBsOeQjNjS8YZIkCIw4i s44130 assertion
has provenance: NP57510.RAcColOyJUX87Mo3rBCNHTBsOeQjNjS8YZIkCIw4i s44130 provenance
has publication info: NP57510.RAcColOyJUX87Mo3rBCNHTBsOeQjNjS8YZIkCIw4i s44130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57510.RAcColOyJUX87Mo3rBCNHTBsOeQjNjS8YZIkCIw4i s44130 assertion
type: Assertion
description: [We have also sequenced a selected material of 37 sporadic cases of more severe hypospadias for mutations in the androgen receptor AR, SRD5A2, and 17beta-hydroxysteroid dehydrogenase HSD17B3 genes and found only two previously described mutations, one in the AR and one in the SRD5A2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16174723
was generated by: ECO_0000203

NP57515.RARDpScaNaT4RJbWg42mFGV4JIR NhhsPOuw shdrPoyw
has assertion: NP57515.RARDpScaNaT4RJbWg42mFGV4JIR NhhsPOuw shdrPoyw130 assertion
has provenance: NP57515.RARDpScaNaT4RJbWg42mFGV4JIR NhhsPOuw shdrPoyw130 provenance
has publication info: NP57515.RARDpScaNaT4RJbWg42mFGV4JIR NhhsPOuw shdrPoyw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57515.RARDpScaNaT4RJbWg42mFGV4JIR NhhsPOuw shdrPoyw130 assertion
type: Assertion
description: [Dietary isoflavone intake, polymorphisms in the CYP17, CYP19, 17beta-HSD1, and SHBG genes, and risk of breast cancer in case-control studies in Japanese, Japanese Brazilians, and non-Japanese Brazilians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20432167
was generated by: ECO_0000203

NP57519.RAQEi8fI3O 5rv6JWf k CaobC3WJu-PF9aV9vEYlC2CM
has assertion: NP57519.RAQEi8fI3O 5rv6JWf k CaobC3WJu-PF9aV9vEYlC2CM130 assertion
has provenance: NP57519.RAQEi8fI3O 5rv6JWf k CaobC3WJu-PF9aV9vEYlC2CM130 provenance
has publication info: NP57519.RAQEi8fI3O 5rv6JWf k CaobC3WJu-PF9aV9vEYlC2CM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57519.RAQEi8fI3O 5rv6JWf k CaobC3WJu-PF9aV9vEYlC2CM130 assertion
type: Assertion
description: [Genetic polymorphisms of estrogen metabolizing enzyme and breast cancer risk in Thai women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19415745
was generated by: ECO_0000203

NP57520.RAfQLrGyx2b BbYe2VnmCvu7oykYnU31fOxTp3vYwgKgE
has assertion: NP57520.RAfQLrGyx2b BbYe2VnmCvu7oykYnU31fOxTp3vYwgKgE130 assertion
has provenance: NP57520.RAfQLrGyx2b BbYe2VnmCvu7oykYnU31fOxTp3vYwgKgE130 provenance
has publication info: NP57520.RAfQLrGyx2b BbYe2VnmCvu7oykYnU31fOxTp3vYwgKgE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57520.RAfQLrGyx2b BbYe2VnmCvu7oykYnU31fOxTp3vYwgKgE130 assertion
type: Assertion
description: [it is unlikely that common genetic variation in HSD17B1 is associated with a moderate modulation in breast cancer risk overall; however, we cannot exclude the possibility of a very weak effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18843021
was generated by: ECO_0000203

NP57524.RAUgWIVt0ryWopkXzuumTqVRCm7Wi6tj8h-3f9-NIV51o
has assertion: NP57524.RAUgWIVt0ryWopkXzuumTqVRCm7Wi6tj8h-3f9-NIV51o130 assertion
has provenance: NP57524.RAUgWIVt0ryWopkXzuumTqVRCm7Wi6tj8h-3f9-NIV51o130 provenance
has publication info: NP57524.RAUgWIVt0ryWopkXzuumTqVRCm7Wi6tj8h-3f9-NIV51o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57524.RAUgWIVt0ryWopkXzuumTqVRCm7Wi6tj8h-3f9-NIV51o130 assertion
type: Assertion
description: [Evaluation of genetic variations in the androgen and estrogen metabolic pathways as risk factors for sporadic and familial prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17507624
was generated by: ECO_0000203

NP57528.RAauVEV6RzssoEEh0WVKVhnAQAU5dkdk8CZT wa95lNyk
has assertion: NP57528.RAauVEV6RzssoEEh0WVKVhnAQAU5dkdk8CZT wa95lNyk130 assertion
has provenance: NP57528.RAauVEV6RzssoEEh0WVKVhnAQAU5dkdk8CZT wa95lNyk130 provenance
has publication info: NP57528.RAauVEV6RzssoEEh0WVKVhnAQAU5dkdk8CZT wa95lNyk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57528.RAauVEV6RzssoEEh0WVKVhnAQAU5dkdk8CZT wa95lNyk130 assertion
type: Assertion
description: [Role of HSD11B2 polymorphisms in essential hypertension and the diuretic response to thiazides.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15673310
was generated by: ECO_0000203

NP57530.RASTsATmBXrxP86fYR0KwXNXxyn80r1uPk6QbgXDyRveY
has assertion: NP57530.RASTsATmBXrxP86fYR0KwXNXxyn80r1uPk6QbgXDyRveY130 assertion
has provenance: NP57530.RASTsATmBXrxP86fYR0KwXNXxyn80r1uPk6QbgXDyRveY130 provenance
has publication info: NP57530.RASTsATmBXrxP86fYR0KwXNXxyn80r1uPk6QbgXDyRveY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57530.RASTsATmBXrxP86fYR0KwXNXxyn80r1uPk6QbgXDyRveY130 assertion
type: Assertion
description: [Genetic association of 11 beta-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/8794836
was generated by: ECO_0000203

NP57537.RAbTo6EndcV5BJb2gpfA-AJxSaOx-JNgPJivb7B719IY0
has assertion: NP57537.RAbTo6EndcV5BJb2gpfA-AJxSaOx-JNgPJivb7B719IY0130 assertion
has provenance: NP57537.RAbTo6EndcV5BJb2gpfA-AJxSaOx-JNgPJivb7B719IY0130 provenance
has publication info: NP57537.RAbTo6EndcV5BJb2gpfA-AJxSaOx-JNgPJivb7B719IY0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57537.RAbTo6EndcV5BJb2gpfA-AJxSaOx-JNgPJivb7B719IY0130 assertion
type: Assertion
description: [over-representation of individuals homozygous for the G534 allele in hypertensive patients compared with control subjects suggests that a mutation in linkage disequilibrium with the G534A polymorphism could increase susceptibility to primary hypertension]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11114699
was generated by: ECO_0000203

NP57539.RAcdg042CQ27zGOe-1mn7Acldy7Q8NhnMTaKRs4dx6hgg
has assertion: NP57539.RAcdg042CQ27zGOe-1mn7Acldy7Q8NhnMTaKRs4dx6hgg130 assertion
has provenance: NP57539.RAcdg042CQ27zGOe-1mn7Acldy7Q8NhnMTaKRs4dx6hgg130 provenance
has publication info: NP57539.RAcdg042CQ27zGOe-1mn7Acldy7Q8NhnMTaKRs4dx6hgg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57539.RAcdg042CQ27zGOe-1mn7Acldy7Q8NhnMTaKRs4dx6hgg130 assertion
type: Assertion
description: [Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19141999
was generated by: ECO_0000203

NP57546.RAeZR9Rr2JSjbmsgpkZZPDwgZBMSa7NvQ-7et5y4Lcuqc
has assertion: NP57546.RAeZR9Rr2JSjbmsgpkZZPDwgZBMSa7NvQ-7et5y4Lcuqc130 assertion
has provenance: NP57546.RAeZR9Rr2JSjbmsgpkZZPDwgZBMSa7NvQ-7et5y4Lcuqc130 provenance
has publication info: NP57546.RAeZR9Rr2JSjbmsgpkZZPDwgZBMSa7NvQ-7et5y4Lcuqc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57546.RAeZR9Rr2JSjbmsgpkZZPDwgZBMSa7NvQ-7et5y4Lcuqc130 assertion
type: Assertion
description: [We have concluded that the participation of these variants in the disorder is unlikely, particularly in view of their apparent lack of function and unlikely influence on receptor expression. However their nature alludes to the potential presence of other more important alterations further along these regions, where sequences encoding alternate promoters have recently been identified for each receptor that may yet be found to harbour such polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12429384
was generated by: ECO_0000203

NP57548.RAR8jX bgkarABce BPpzSReaJqKDijD10Xq4dEbSvWmQ
has assertion: NP57548.RAR8jX bgkarABce BPpzSReaJqKDijD10Xq4dEbSvWmQ130 assertion
has provenance: NP57548.RAR8jX bgkarABce BPpzSReaJqKDijD10Xq4dEbSvWmQ130 provenance
has publication info: NP57548.RAR8jX bgkarABce BPpzSReaJqKDijD10Xq4dEbSvWmQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57548.RAR8jX bgkarABce BPpzSReaJqKDijD10Xq4dEbSvWmQ130 assertion
type: Assertion
description: [Low-penetrance genes and their involvement in colorectal cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12433710
was generated by: ECO_0000203

NP57551.RAaRhIVg5u36OJkLzMmMajRJ6xygp4C7r1ZR-udi 4PkY
has assertion: NP57551.RAaRhIVg5u36OJkLzMmMajRJ6xygp4C7r1ZR-udi 4PkY130 assertion
has provenance: NP57551.RAaRhIVg5u36OJkLzMmMajRJ6xygp4C7r1ZR-udi 4PkY130 provenance
has publication info: NP57551.RAaRhIVg5u36OJkLzMmMajRJ6xygp4C7r1ZR-udi 4PkY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57551.RAaRhIVg5u36OJkLzMmMajRJ6xygp4C7r1ZR-udi 4PkY130 assertion
type: Assertion
description: [ K- ras gene mutations occur in chronic pancreatitis and are associated with evolution towards PAC. The absence of pancreatic calcifications and the presence of exocrine insufficiency were identified as additional predictive factors for the development of PAC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15202051
was generated by: ECO_0000203

NP57554.RAdiZN5K8fwHKz3stxshKo7-rxaHorSWSaL2EsbvF2idI
has assertion: NP57554.RAdiZN5K8fwHKz3stxshKo7-rxaHorSWSaL2EsbvF2idI130 assertion
has provenance: NP57554.RAdiZN5K8fwHKz3stxshKo7-rxaHorSWSaL2EsbvF2idI130 provenance
has publication info: NP57554.RAdiZN5K8fwHKz3stxshKo7-rxaHorSWSaL2EsbvF2idI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57554.RAdiZN5K8fwHKz3stxshKo7-rxaHorSWSaL2EsbvF2idI130 assertion
type: Assertion
description: [We conclude that individuals harboring the homozygous 81C-genotype of the H-ras proto-oncogene are at an increased risk of bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12540507
was generated by: ECO_0000203

NP57557.RARil3guaZIbkzHO1sGJ X7XFuzFUdQJXTQDkx827e4rM
has assertion: NP57557.RARil3guaZIbkzHO1sGJ X7XFuzFUdQJXTQDkx827e4rM130 assertion
has provenance: NP57557.RARil3guaZIbkzHO1sGJ X7XFuzFUdQJXTQDkx827e4rM130 provenance
has publication info: NP57557.RARil3guaZIbkzHO1sGJ X7XFuzFUdQJXTQDkx827e4rM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57557.RARil3guaZIbkzHO1sGJ X7XFuzFUdQJXTQDkx827e4rM130 assertion
type: Assertion
description: [Frequency of active ras oncogenes in human bladder cancers associated with schistosomiasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/3117747
was generated by: ECO_0000203

NP57559.RAThEtCEbrjY7hqkAaxvTM 3eH468w-FQr8VaysW933c
has assertion: NP57559.RAThEtCEbrjY7hqkAaxvTM 3eH468w-FQr8VaysW933c130 assertion
has provenance: NP57559.RAThEtCEbrjY7hqkAaxvTM 3eH468w-FQr8VaysW933c130 provenance
has publication info: NP57559.RAThEtCEbrjY7hqkAaxvTM 3eH468w-FQr8VaysW933c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57559.RAThEtCEbrjY7hqkAaxvTM 3eH468w-FQr8VaysW933c130 assertion
type: Assertion
description: [The aim of this study w trial randomized as to investigate the frequencies of human papillomavirus (HPV) and mutation in Ha-ras oncogene and tumour suppressor p53 gene in cervical cancer and precursor lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11436698
was generated by: ECO_0000203

NP57566.RAU2s23mEpIK47ggL0HRKrwWuhXP7NxVa352k1at2d46M
has assertion: NP57566.RAU2s23mEpIK47ggL0HRKrwWuhXP7NxVa352k1at2d46M130 assertion
has provenance: NP57566.RAU2s23mEpIK47ggL0HRKrwWuhXP7NxVa352k1at2d46M130 provenance
has publication info: NP57566.RAU2s23mEpIK47ggL0HRKrwWuhXP7NxVa352k1at2d46M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57566.RAU2s23mEpIK47ggL0HRKrwWuhXP7NxVa352k1at2d46M130 assertion
type: Assertion
description: [Multivariate logistic regression analysis with adjustment for age, body mass index, presence of hyperlipidemia, diabetes mellitus, and current smoking and drinking revealed that one single nucleotide polymorphism (SNP), IMS-JST126186, in HPCAL1 (hippocalcin-like 1) in women and two SNPs, IMS-JST149391 and IMS-JST149390, in GREB1 (gene regulated by estrogen in breast cancer 1) in men were significantly associated with both prevalence of hypertension and blood pressure levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15834280
was generated by: ECO_0000203

NP57573.RAcs7EMktSEpu9F31kmk0y 0Nspjhcw yn2QZuTq4NrDo
has assertion: NP57573.RAcs7EMktSEpu9F31kmk0y 0Nspjhcw yn2QZuTq4NrDo130 assertion
has provenance: NP57573.RAcs7EMktSEpu9F31kmk0y 0Nspjhcw yn2QZuTq4NrDo130 provenance
has publication info: NP57573.RAcs7EMktSEpu9F31kmk0y 0Nspjhcw yn2QZuTq4NrDo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57573.RAcs7EMktSEpu9F31kmk0y 0Nspjhcw yn2QZuTq4NrDo130 assertion
type: Assertion
description: [in contrast to the findings from cross-sectionally based studies, the results from this longitudinal study show that Hp 1-1 individuals are at elevated risk for CHD mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11427216
was generated by: ECO_0000203

NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr g4PcVpWhFK5U
has assertion: NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr g4PcVpWhFK5U130 assertion
has provenance: NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr g4PcVpWhFK5U130 provenance
has publication info: NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr g4PcVpWhFK5U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr g4PcVpWhFK5U130 assertion
type: Assertion
description: [These results suggest that haptoglobin phenotype is an important risk factor in determining susceptibility to cardiovascular disease in obstructive sleep apnea syndrome, which may be mediated by the decreased antioxidant and antiinflammatory actions of the haptoglobin 2 allelic protein product.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12938813
was generated by: ECO_0000203

NP57582.RAXABiHCCWlAdx5R0jdKSX4I-MGVOO3FFtAOmCJJxqnI4
has assertion: NP57582.RAXABiHCCWlAdx5R0jdKSX4I-MGVOO3FFtAOmCJJxqnI4130 assertion
has provenance: NP57582.RAXABiHCCWlAdx5R0jdKSX4I-MGVOO3FFtAOmCJJxqnI4130 provenance
has publication info: NP57582.RAXABiHCCWlAdx5R0jdKSX4I-MGVOO3FFtAOmCJJxqnI4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57582.RAXABiHCCWlAdx5R0jdKSX4I-MGVOO3FFtAOmCJJxqnI4130 assertion
type: Assertion
description: [Histamine N-methyltransferase pharmacogenetics: association of a common functional polymorphism with asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10803682
was generated by: ECO_0000203

NP57585.RAXmvYKGH2-NfjUqLakeVVGchyzY90fr2MMGRy70aZTfs
has assertion: NP57585.RAXmvYKGH2-NfjUqLakeVVGchyzY90fr2MMGRy70aZTfs130 assertion
has provenance: NP57585.RAXmvYKGH2-NfjUqLakeVVGchyzY90fr2MMGRy70aZTfs130 provenance
has publication info: NP57585.RAXmvYKGH2-NfjUqLakeVVGchyzY90fr2MMGRy70aZTfs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57585.RAXmvYKGH2-NfjUqLakeVVGchyzY90fr2MMGRy70aZTfs130 assertion
type: Assertion
description: [These findings suggest that combination of several polymorphisms in the enzymes that activate or detoxify the tobacco smoke, such as EPHX1 and HMOX1, might be associated with its affects on the development of emphysematous changes of the lung.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12579334
was generated by: ECO_0000203

NP57589.RAdpxszcXKRHBXS3ets-CklroGrwEIG-jnqionZp0SIKI
has assertion: NP57589.RAdpxszcXKRHBXS3ets-CklroGrwEIG-jnqionZp0SIKI130 assertion
has provenance: NP57589.RAdpxszcXKRHBXS3ets-CklroGrwEIG-jnqionZp0SIKI130 provenance
has publication info: NP57589.RAdpxszcXKRHBXS3ets-CklroGrwEIG-jnqionZp0SIKI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57589.RAdpxszcXKRHBXS3ets-CklroGrwEIG-jnqionZp0SIKI130 assertion
type: Assertion
description: [Association of an intronic variant of the heme oxygenase-1 gene with hypertension in northern Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19886851
was generated by: ECO_0000203

NP57590.RAXupkH7-xpP2MI2VWD9KnNvlBjn8PxIrD4 TTDQ-n9k0
has assertion: NP57590.RAXupkH7-xpP2MI2VWD9KnNvlBjn8PxIrD4 TTDQ-n9k0130 assertion
has provenance: NP57590.RAXupkH7-xpP2MI2VWD9KnNvlBjn8PxIrD4 TTDQ-n9k0130 provenance
has publication info: NP57590.RAXupkH7-xpP2MI2VWD9KnNvlBjn8PxIrD4 TTDQ-n9k0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57590.RAXupkH7-xpP2MI2VWD9KnNvlBjn8PxIrD4 TTDQ-n9k0130 assertion
type: Assertion
description: [ The HO-1 promoter genotype that controls the degree of HO-1 up-regulation in response to stress stimuli is associated with the postintervention inflammatory response and the restenosis risk after balloon angioplasty.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15028349
was generated by: ECO_0000203

NP57607.RASr7hOEqm55GHYBXHzGRpBixzOlwG7oqJ1wQmModVNjg
has assertion: NP57607.RASr7hOEqm55GHYBXHzGRpBixzOlwG7oqJ1wQmModVNjg130 assertion
has provenance: NP57607.RASr7hOEqm55GHYBXHzGRpBixzOlwG7oqJ1wQmModVNjg130 provenance
has publication info: NP57607.RASr7hOEqm55GHYBXHzGRpBixzOlwG7oqJ1wQmModVNjg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57607.RASr7hOEqm55GHYBXHzGRpBixzOlwG7oqJ1wQmModVNjg130 assertion
type: Assertion
description: [Association between heme oxygenase-1 gene promoter polymorphisms and type 2 diabetes in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19696228
was generated by: ECO_0000203

NP57613.RASC3eQP16kox7eZkdeZCQH6 ZUm-Tu Ah1FMhNqQh0wM
has assertion: NP57613.RASC3eQP16kox7eZkdeZCQH6 ZUm-Tu Ah1FMhNqQh0wM130 assertion
has provenance: NP57613.RASC3eQP16kox7eZkdeZCQH6 ZUm-Tu Ah1FMhNqQh0wM130 provenance
has publication info: NP57613.RASC3eQP16kox7eZkdeZCQH6 ZUm-Tu Ah1FMhNqQh0wM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57613.RASC3eQP16kox7eZkdeZCQH6 ZUm-Tu Ah1FMhNqQh0wM130 assertion
type: Assertion
description: [Gene-gene interaction between heme oxygenase-1 and liver X receptor-beta and Alzheimer's disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18597895
was generated by: ECO_0000203

NP57614.RAXeat0lSVUo4HAgzF2iG14Ao5SwZ4XYGnpp7-I8Dv01M
has assertion: NP57614.RAXeat0lSVUo4HAgzF2iG14Ao5SwZ4XYGnpp7-I8Dv01M130 assertion
has provenance: NP57614.RAXeat0lSVUo4HAgzF2iG14Ao5SwZ4XYGnpp7-I8Dv01M130 provenance
has publication info: NP57614.RAXeat0lSVUo4HAgzF2iG14Ao5SwZ4XYGnpp7-I8Dv01M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57614.RAXeat0lSVUo4HAgzF2iG14Ao5SwZ4XYGnpp7-I8Dv01M130 assertion
type: Assertion
description: [Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19141999
was generated by: ECO_0000203

NP57616.RAVPLdZUZS4KF7cxIBendre sqq 5jordhvH72wHCbeAQ
has assertion: NP57616.RAVPLdZUZS4KF7cxIBendre sqq 5jordhvH72wHCbeAQ130 assertion
has provenance: NP57616.RAVPLdZUZS4KF7cxIBendre sqq 5jordhvH72wHCbeAQ130 provenance
has publication info: NP57616.RAVPLdZUZS4KF7cxIBendre sqq 5jordhvH72wHCbeAQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57616.RAVPLdZUZS4KF7cxIBendre sqq 5jordhvH72wHCbeAQ130 assertion
type: Assertion
description: [Acute intermittent porphyria (AIP), resulting from a deficiency of porphobilinogen deaminase (PBGD) in heme biosynthesis, is genetically heterogeneous and manifests with variable penetrance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15643298
was generated by: ECO_0000203

NP57618.RAf n JxHavncf0EklvaRBl18IXEzCxABlQZTXdL3WMOY
has assertion: NP57618.RAf n JxHavncf0EklvaRBl18IXEzCxABlQZTXdL3WMOY130 assertion
has provenance: NP57618.RAf n JxHavncf0EklvaRBl18IXEzCxABlQZTXdL3WMOY130 provenance
has publication info: NP57618.RAf n JxHavncf0EklvaRBl18IXEzCxABlQZTXdL3WMOY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57618.RAf n JxHavncf0EklvaRBl18IXEzCxABlQZTXdL3WMOY130 assertion
type: Assertion
description: [Thus we provide the first evidence for a possible role of HLA-G in genetic susceptibility to, and pathogenesis of pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11766889
was generated by: ECO_0000203

NP57619.RAQDy cmaA1ccR9klhYlvGNZD7i-IHL5AjgHr7QRSsx-s
has assertion: NP57619.RAQDy cmaA1ccR9klhYlvGNZD7i-IHL5AjgHr7QRSsx-s130 assertion
has provenance: NP57619.RAQDy cmaA1ccR9klhYlvGNZD7i-IHL5AjgHr7QRSsx-s130 provenance
has publication info: NP57619.RAQDy cmaA1ccR9klhYlvGNZD7i-IHL5AjgHr7QRSsx-s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57619.RAQDy cmaA1ccR9klhYlvGNZD7i-IHL5AjgHr7QRSsx-s130 assertion
type: Assertion
description: [The HLA-G 14bp gene polymorphism and decidual HLA-G 14bp gene expression in pre-eclamptic and normal pregnancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18423887
was generated by: ECO_0000203

NP57626.RAd70JJmwdw1DcTTtH6Mb1dVtPUo1TsysHkWgTC4yhQAE
has assertion: NP57626.RAd70JJmwdw1DcTTtH6Mb1dVtPUo1TsysHkWgTC4yhQAE130 assertion
has provenance: NP57626.RAd70JJmwdw1DcTTtH6Mb1dVtPUo1TsysHkWgTC4yhQAE130 provenance
has publication info: NP57626.RAd70JJmwdw1DcTTtH6Mb1dVtPUo1TsysHkWgTC4yhQAE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57626.RAd70JJmwdw1DcTTtH6Mb1dVtPUo1TsysHkWgTC4yhQAE130 assertion
type: Assertion
description: [ The allele frequencies of HLA-E are 42.29% for E*0101, 24.88% and 32.84% for E*01031 and E*01032 respectively in Shanghai Chinese. No extensive linkage disequilibrium was found between HLA-E and HLA-A or -B locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11774212
was generated by: ECO_0000203

NP57628.RAX4GWtcsqBS CTjvUx-p4eNeugkXYLVEJbBdRxVVSSdI
has assertion: NP57628.RAX4GWtcsqBS CTjvUx-p4eNeugkXYLVEJbBdRxVVSSdI130 assertion
has provenance: NP57628.RAX4GWtcsqBS CTjvUx-p4eNeugkXYLVEJbBdRxVVSSdI130 provenance
has publication info: NP57628.RAX4GWtcsqBS CTjvUx-p4eNeugkXYLVEJbBdRxVVSSdI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57628.RAX4GWtcsqBS CTjvUx-p4eNeugkXYLVEJbBdRxVVSSdI130 assertion
type: Assertion
description: [Our study provides the first demonstration of the association of the polymorphism of the MHC2TA gene with genetic risk for AAD that appears to be independent from the well-known association with the polymorphism of HLA class II genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16849401
was generated by: ECO_0000203

NP57630.RAdZo7jETbUpF7iVTY4YChJIcpQo7j1XFyOLyku7Zxx4Y
has assertion: NP57630.RAdZo7jETbUpF7iVTY4YChJIcpQo7j1XFyOLyku7Zxx4Y130 assertion
has provenance: NP57630.RAdZo7jETbUpF7iVTY4YChJIcpQo7j1XFyOLyku7Zxx4Y130 provenance
has publication info: NP57630.RAdZo7jETbUpF7iVTY4YChJIcpQo7j1XFyOLyku7Zxx4Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57630.RAdZo7jETbUpF7iVTY4YChJIcpQo7j1XFyOLyku7Zxx4Y130 assertion
type: Assertion
description: [ Alleles HLA-DR6 (13) were significantly implicated in their susceptibility to GDM. Conversely, HLA-DR2 (15), HLA-DR51 alleles might confer protection against GDM. HLA-DR3 gene and HLA-DR6 (13)/DR9 heterozygote were associated with severity and prognosis of GDM. It may be a marker of grade and prognosis of GDM and may direct the treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12133402
was generated by: ECO_0000203

NP57636.RAcGH3rOJ4C -AZVIecv-DfdNFbbT6fTduO HTX 2jRGw
has assertion: NP57636.RAcGH3rOJ4C -AZVIecv-DfdNFbbT6fTduO HTX 2jRGw130 assertion
has provenance: NP57636.RAcGH3rOJ4C -AZVIecv-DfdNFbbT6fTduO HTX 2jRGw130 provenance
has publication info: NP57636.RAcGH3rOJ4C -AZVIecv-DfdNFbbT6fTduO HTX 2jRGw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57636.RAcGH3rOJ4C -AZVIecv-DfdNFbbT6fTduO HTX 2jRGw130 assertion
type: Assertion
description: [Polymorphisms of genes in the human leukocyte antigen (HLA) complex, particularly those encoding HLA-DR, have been suggested as markers of susceptibility to Kaposi's sarcoma (KS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15902698
was generated by: ECO_0000203

NP57640.RAVzkqA1hZKeL9k6M3YGESrcD5rD2euGbgceXDz6Tidq8
has assertion: NP57640.RAVzkqA1hZKeL9k6M3YGESrcD5rD2euGbgceXDz6Tidq8130 assertion
has provenance: NP57640.RAVzkqA1hZKeL9k6M3YGESrcD5rD2euGbgceXDz6Tidq8130 provenance
has publication info: NP57640.RAVzkqA1hZKeL9k6M3YGESrcD5rD2euGbgceXDz6Tidq8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57640.RAVzkqA1hZKeL9k6M3YGESrcD5rD2euGbgceXDz6Tidq8130 assertion
type: Assertion
description: [HLA-DRB1 * 0301.2 and HLA-DRB4 * 0101 alleles might confer protection against AR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12541760
was generated by: ECO_0000203

NP57643.RAeYxRJhnxH8foLkqKyItsmzuZ EczVZhWNaLgEcu61MQ
has assertion: NP57643.RAeYxRJhnxH8foLkqKyItsmzuZ EczVZhWNaLgEcu61MQ130 assertion
has provenance: NP57643.RAeYxRJhnxH8foLkqKyItsmzuZ EczVZhWNaLgEcu61MQ130 provenance
has publication info: NP57643.RAeYxRJhnxH8foLkqKyItsmzuZ EczVZhWNaLgEcu61MQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:27+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP57643.RAeYxRJhnxH8foLkqKyItsmzuZ EczVZhWNaLgEcu61MQ130 assertion
type: Assertion
description: [The allelic frequencies of HLA-A*30, Cw*06, DRB1*07, and DQB1*0201 were increased significantly in generalized vitiligo and especially in the patients without family history compared with the controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17407088
was generated by: ECO_0000203