NP65935.RAevhV7K ec1M7dnW8vmiIivi9GFST6g-LHiE6m9iewfo
has assertion: NP65935.RAevhV7K ec1M7dnW8vmiIivi9GFST6g-LHiE6m9iewfo130 assertion
has provenance: NP65935.RAevhV7K ec1M7dnW8vmiIivi9GFST6g-LHiE6m9iewfo130 provenance
has publication info: NP65935.RAevhV7K ec1M7dnW8vmiIivi9GFST6g-LHiE6m9iewfo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65935.RAevhV7K ec1M7dnW8vmiIivi9GFST6g-LHiE6m9iewfo130 assertion
type: Assertion
description: [Pharmacogenetics of MXA SNPs in interferon-beta treated 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/17126411
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

NP65941.RARYr31jtdouwsJMfw2l3r7sRzhbvsLYOKbsZCWTCTRuQ
has assertion: NP65941.RARYr31jtdouwsJMfw2l3r7sRzhbvsLYOKbsZCWTCTRuQ130 assertion
has provenance: NP65941.RARYr31jtdouwsJMfw2l3r7sRzhbvsLYOKbsZCWTCTRuQ130 provenance
has publication info: NP65941.RARYr31jtdouwsJMfw2l3r7sRzhbvsLYOKbsZCWTCTRuQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65941.RARYr31jtdouwsJMfw2l3r7sRzhbvsLYOKbsZCWTCTRuQ130 assertion
type: Assertion
description: [Genetic analyses of celiac disease in a Spanish population confirm association with CELIAC3 but not with CELIAC4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17767555
was generated by: ECO_0000203

NP65943.RAROXYNWPApfbPBB-WPjXPVlpOcO6xDDKo57 pFod38qE
has assertion: NP65943.RAROXYNWPApfbPBB-WPjXPVlpOcO6xDDKo57 pFod38qE130 assertion
has provenance: NP65943.RAROXYNWPApfbPBB-WPjXPVlpOcO6xDDKo57 pFod38qE130 provenance
has publication info: NP65943.RAROXYNWPApfbPBB-WPjXPVlpOcO6xDDKo57 pFod38qE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65943.RAROXYNWPApfbPBB-WPjXPVlpOcO6xDDKo57 pFod38qE130 assertion
type: Assertion
description: [Genotyping of MYO9B and molecular HLA-DQ2 typing were performed on 62 RCD II and EATL patients, 421 uncomplicated CD patients, and 1624 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/17967566
was generated by: ECO_0000203

NP65944.RASI89TSJqFx3Voy3fRPdY3jjp2Y4fe03gReZyX-vbBG4
has assertion: NP65944.RASI89TSJqFx3Voy3fRPdY3jjp2Y4fe03gReZyX-vbBG4130 assertion
has provenance: NP65944.RASI89TSJqFx3Voy3fRPdY3jjp2Y4fe03gReZyX-vbBG4130 provenance
has publication info: NP65944.RASI89TSJqFx3Voy3fRPdY3jjp2Y4fe03gReZyX-vbBG4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65944.RASI89TSJqFx3Voy3fRPdY3jjp2Y4fe03gReZyX-vbBG4130 assertion
type: Assertion
description: [Linkage and association was shown between the MYOC polymorphisms and high myopia in our family-based association study. The SNP rs235858 at the 3 flanking region showed the highest degree of confidence for 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/17438518
was generated by: ECO_0000203

NP65949.RAfUEBJD1c7pAn2XC-z3DNwRiXrBxnX2IIICyj-oRT4P4
has assertion: NP65949.RAfUEBJD1c7pAn2XC-z3DNwRiXrBxnX2IIICyj-oRT4P4130 assertion
has provenance: NP65949.RAfUEBJD1c7pAn2XC-z3DNwRiXrBxnX2IIICyj-oRT4P4130 provenance
has publication info: NP65949.RAfUEBJD1c7pAn2XC-z3DNwRiXrBxnX2IIICyj-oRT4P4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65949.RAfUEBJD1c7pAn2XC-z3DNwRiXrBxnX2IIICyj-oRT4P4130 assertion
type: Assertion
description: [Our study supports NAPG as a candidate for 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/19429185
was generated by: ECO_0000203

NP65950.RATD6QE0is4PoTmxNu1RH-4-iI0r0GPFZLc4eVEhkLdQI
has assertion: NP65950.RATD6QE0is4PoTmxNu1RH-4-iI0r0GPFZLc4eVEhkLdQI130 assertion
has provenance: NP65950.RATD6QE0is4PoTmxNu1RH-4-iI0r0GPFZLc4eVEhkLdQI130 provenance
has publication info: NP65950.RATD6QE0is4PoTmxNu1RH-4-iI0r0GPFZLc4eVEhkLdQI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65950.RATD6QE0is4PoTmxNu1RH-4-iI0r0GPFZLc4eVEhkLdQI130 assertion
type: Assertion
description: [Our findings suggest that HTR5A gene could play an important role in the pathogenesis of bipolar disorder 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/19328558
was generated by: ECO_0000203

NP65954.RAdESOy-68Ojf4qE2bf fLYXTNiKjoCMt9qE73D4qwpWw
has assertion: NP65954.RAdESOy-68Ojf4qE2bf fLYXTNiKjoCMt9qE73D4qwpWw130 assertion
has provenance: NP65954.RAdESOy-68Ojf4qE2bf fLYXTNiKjoCMt9qE73D4qwpWw130 provenance
has publication info: NP65954.RAdESOy-68Ojf4qE2bf fLYXTNiKjoCMt9qE73D4qwpWw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65954.RAdESOy-68Ojf4qE2bf fLYXTNiKjoCMt9qE73D4qwpWw130 assertion
type: Assertion
description: [We also evaluated the association between GSTs and NAT2 and the risk factors for gastric cancer such as alcohol consumption, smoking, H. pylori infection, family history of gastric cancer, and tumor location.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16615268
was generated by: ECO_0000203

NP65958.RAfnf2Kn2sDhfKoPZC83bSkZROHnbJBRVLzeCvPmETSB8
has assertion: NP65958.RAfnf2Kn2sDhfKoPZC83bSkZROHnbJBRVLzeCvPmETSB8130 assertion
has provenance: NP65958.RAfnf2Kn2sDhfKoPZC83bSkZROHnbJBRVLzeCvPmETSB8130 provenance
has publication info: NP65958.RAfnf2Kn2sDhfKoPZC83bSkZROHnbJBRVLzeCvPmETSB8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65958.RAfnf2Kn2sDhfKoPZC83bSkZROHnbJBRVLzeCvPmETSB8130 assertion
type: Assertion
description: [Increased risk of gastrointestinal lymphoma in carriers of the 657del5 NBS1 gene 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/16998789
was generated by: ECO_0000203

NP65959.RAU O5Kqg-mkAGgykbh2p4XuTh5MdXTG1jCN7tJfNsM8A
has assertion: NP65959.RAU O5Kqg-mkAGgykbh2p4XuTh5MdXTG1jCN7tJfNsM8A130 assertion
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has publication info: NP65959.RAU O5Kqg-mkAGgykbh2p4XuTh5MdXTG1jCN7tJfNsM8A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65959.RAU O5Kqg-mkAGgykbh2p4XuTh5MdXTG1jCN7tJfNsM8A130 assertion
type: Assertion
description: [Association analyses of NCR3 polymorphisms with P. falciparum mild 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/17208487
was generated by: ECO_0000203

NP65960.RAUuLg7nUH9IPYcLlp24pphpUm xwutRiecgyYmGsIIJA
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has publication info: NP65960.RAUuLg7nUH9IPYcLlp24pphpUm xwutRiecgyYmGsIIJA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65960.RAUuLg7nUH9IPYcLlp24pphpUm xwutRiecgyYmGsIIJA130 assertion
type: Assertion
description: [Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with schizophrenia 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/16508936
was generated by: ECO_0000203

NP65966.RAdMiy0RWbEnBqzF2yGMqVT1QzvKyetibn3qyDNPyCAsk
has assertion: NP65966.RAdMiy0RWbEnBqzF2yGMqVT1QzvKyetibn3qyDNPyCAsk130 assertion
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has publication info: NP65966.RAdMiy0RWbEnBqzF2yGMqVT1QzvKyetibn3qyDNPyCAsk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65966.RAdMiy0RWbEnBqzF2yGMqVT1QzvKyetibn3qyDNPyCAsk130 assertion
type: Assertion
description: [Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17470137
was generated by: ECO_0000203

NP65977.RAVPLYgO0EXkGkPn3-SRx qHviNNuHzdxJ7xcyZwUNWT4
has assertion: NP65977.RAVPLYgO0EXkGkPn3-SRx qHviNNuHzdxJ7xcyZwUNWT4130 assertion
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has publication info: NP65977.RAVPLYgO0EXkGkPn3-SRx qHviNNuHzdxJ7xcyZwUNWT4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65977.RAVPLYgO0EXkGkPn3-SRx qHviNNuHzdxJ7xcyZwUNWT4130 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

NP65978.RAeOeyiny o9VdmyR4OZjIGONP yZ3pypcNC9IfYRyIm4
has assertion: NP65978.RAeOeyiny o9VdmyR4OZjIGONP yZ3pypcNC9IfYRyIm4130 assertion
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has publication info: NP65978.RAeOeyiny o9VdmyR4OZjIGONP yZ3pypcNC9IfYRyIm4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65978.RAeOeyiny o9VdmyR4OZjIGONP yZ3pypcNC9IfYRyIm4130 assertion
type: Assertion
description: [Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's 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/17554261
was generated by: ECO_0000203

NP65989.RAQjdViTBmVm2LEWxgNCfimV6hdEe1EM4dUREozHlFxAg
has assertion: NP65989.RAQjdViTBmVm2LEWxgNCfimV6hdEe1EM4dUREozHlFxAg130 assertion
has provenance: NP65989.RAQjdViTBmVm2LEWxgNCfimV6hdEe1EM4dUREozHlFxAg130 provenance
has publication info: NP65989.RAQjdViTBmVm2LEWxgNCfimV6hdEe1EM4dUREozHlFxAg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65989.RAQjdViTBmVm2LEWxgNCfimV6hdEe1EM4dUREozHlFxAg130 assertion
type: Assertion
description: [We found that intracellular Propionibacterium acnes, a possible causative agent of sarcoidosis, activated NF-kappaB in both NOD1- and NOD2-dependent manners.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16935475
was generated by: ECO_0000203

NP65991.RAS7P1BgbhC5lXOMXUqguvaL61cIfiYRr3i32Gruttuuk
has assertion: NP65991.RAS7P1BgbhC5lXOMXUqguvaL61cIfiYRr3i32Gruttuuk130 assertion
has provenance: NP65991.RAS7P1BgbhC5lXOMXUqguvaL61cIfiYRr3i32Gruttuuk130 provenance
has publication info: NP65991.RAS7P1BgbhC5lXOMXUqguvaL61cIfiYRr3i32Gruttuuk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65991.RAS7P1BgbhC5lXOMXUqguvaL61cIfiYRr3i32Gruttuuk130 assertion
type: Assertion
description: [variation in individual genes from the NLR family as well as interactions within this group of innate immune receptor genes could play a role in AD 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/17620097
was generated by: ECO_0000203

NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ
has assertion: NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130 assertion
has provenance: NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130 provenance
has publication info: NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130 assertion
type: Assertion
description: [Our results suggest that the G908R mutation of the CARD15/NOD2 gene, as well as the T allele and TT genotype of the CD14 promoter are associated with increased susceptibility for developing 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/16933467
was generated by: ECO_0000203

NP65995.RARXfKzdiAZB5SIdLj-frat3BJZJgni399RX-pxqIdzTs
has assertion: NP65995.RARXfKzdiAZB5SIdLj-frat3BJZJgni399RX-pxqIdzTs130 assertion
has provenance: NP65995.RARXfKzdiAZB5SIdLj-frat3BJZJgni399RX-pxqIdzTs130 provenance
has publication info: NP65995.RARXfKzdiAZB5SIdLj-frat3BJZJgni399RX-pxqIdzTs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65995.RARXfKzdiAZB5SIdLj-frat3BJZJgni399RX-pxqIdzTs130 assertion
type: Assertion
description: []. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16964084
was generated by: ECO_0000203

NP65996.RAT3Jelwi0cHiMWJfnWZ3Zs2mPHbB8NqnKr9YF fJ3lQA
has assertion: NP65996.RAT3Jelwi0cHiMWJfnWZ3Zs2mPHbB8NqnKr9YF fJ3lQA130 assertion
has provenance: NP65996.RAT3Jelwi0cHiMWJfnWZ3Zs2mPHbB8NqnKr9YF fJ3lQA130 provenance
has publication info: NP65996.RAT3Jelwi0cHiMWJfnWZ3Zs2mPHbB8NqnKr9YF fJ3lQA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65996.RAT3Jelwi0cHiMWJfnWZ3Zs2mPHbB8NqnKr9YF fJ3lQA130 assertion
type: Assertion
description: [We studied gene variants of NOS-I (rs2682826;rs1353939;rs2293049;rs693534) and NOS-III (rs2070744;rs1799983;rs891512) in a total of 571 cases (167 German suicide attempters, 92 Caucasian suicide completers and 312 German healthy 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/17579350
was generated by: ECO_0000203

NP65997.RAfngXNcLLNYWnSQiqcQmvBCFSoy7ogNglmGG4-7vWWQ4
has assertion: NP65997.RAfngXNcLLNYWnSQiqcQmvBCFSoy7ogNglmGG4-7vWWQ4130 assertion
has provenance: NP65997.RAfngXNcLLNYWnSQiqcQmvBCFSoy7ogNglmGG4-7vWWQ4130 provenance
has publication info: NP65997.RAfngXNcLLNYWnSQiqcQmvBCFSoy7ogNglmGG4-7vWWQ4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP65997.RAfngXNcLLNYWnSQiqcQmvBCFSoy7ogNglmGG4-7vWWQ4130 assertion
type: Assertion
description: [To further clarify the possible involvement of NOS1 with suicide, we carried out an association study of NOS1 gene polymorphisms with completed 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/20470850
was generated by: ECO_0000203

NP66000.RAeIDLAt p5tv9mW-2m M-vfLahrWrDUbYAERd4 v-vX4
has assertion: NP66000.RAeIDLAt p5tv9mW-2m M-vfLahrWrDUbYAERd4 v-vX4130 assertion
has provenance: NP66000.RAeIDLAt p5tv9mW-2m M-vfLahrWrDUbYAERd4 v-vX4130 provenance
has publication info: NP66000.RAeIDLAt p5tv9mW-2m M-vfLahrWrDUbYAERd4 v-vX4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66000.RAeIDLAt p5tv9mW-2m M-vfLahrWrDUbYAERd4 v-vX4130 assertion
type: Assertion
description: [Genetic polymorphisms in nitric oxide synthase genes modify the relationship between vegetable and fruit intake and risk of 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/19423521
was generated by: ECO_0000203

NP66002.RAXK pti9uLY43FWXZ6KFahRoHK4NF8jDYXgspRNpoE-g
has assertion: NP66002.RAXK pti9uLY43FWXZ6KFahRoHK4NF8jDYXgspRNpoE-g130 assertion
has provenance: NP66002.RAXK pti9uLY43FWXZ6KFahRoHK4NF8jDYXgspRNpoE-g130 provenance
has publication info: NP66002.RAXK pti9uLY43FWXZ6KFahRoHK4NF8jDYXgspRNpoE-g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66002.RAXK pti9uLY43FWXZ6KFahRoHK4NF8jDYXgspRNpoE-g130 assertion
type: Assertion
description: [This is the first study to identify the repeat polymorphisms in the iNOS gene that are associated with severity of asthma and eosinophils.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17189532
was generated by: ECO_0000203

NP66005.RAdNgLMElHsqtJ0qQMukwdGvZ7eTOVH3-TB3 G8Rz71Lg
has assertion: NP66005.RAdNgLMElHsqtJ0qQMukwdGvZ7eTOVH3-TB3 G8Rz71Lg130 assertion
has provenance: NP66005.RAdNgLMElHsqtJ0qQMukwdGvZ7eTOVH3-TB3 G8Rz71Lg130 provenance
has publication info: NP66005.RAdNgLMElHsqtJ0qQMukwdGvZ7eTOVH3-TB3 G8Rz71Lg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66005.RAdNgLMElHsqtJ0qQMukwdGvZ7eTOVH3-TB3 G8Rz71Lg130 assertion
type: Assertion
description: [A second-generation genomewide screen for asthma-susceptibility alleles in a founder 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/11022011
was generated by: ECO_0000203

NP66010.RARX24uS ydFR3gq C3OMyQ-nrKUxqgK5anT6gWl58G5E
has assertion: NP66010.RARX24uS ydFR3gq C3OMyQ-nrKUxqgK5anT6gWl58G5E130 assertion
has provenance: NP66010.RARX24uS ydFR3gq C3OMyQ-nrKUxqgK5anT6gWl58G5E130 provenance
has publication info: NP66010.RARX24uS ydFR3gq C3OMyQ-nrKUxqgK5anT6gWl58G5E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66010.RARX24uS ydFR3gq C3OMyQ-nrKUxqgK5anT6gWl58G5E130 assertion
type: Assertion
description: [These findings suggest that the polymorphic (CCTTT)n repeat in the iNOS promoter region might be involved in the development of UC, especially in those who have ever smoked.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17482959
was generated by: ECO_0000203

NP66015.RAfbvlVdZlzHRfXQaF5o7CXnY1Unq3J6oEIj1Hy 42wkU
has assertion: NP66015.RAfbvlVdZlzHRfXQaF5o7CXnY1Unq3J6oEIj1Hy 42wkU130 assertion
has provenance: NP66015.RAfbvlVdZlzHRfXQaF5o7CXnY1Unq3J6oEIj1Hy 42wkU130 provenance
has publication info: NP66015.RAfbvlVdZlzHRfXQaF5o7CXnY1Unq3J6oEIj1Hy 42wkU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66015.RAfbvlVdZlzHRfXQaF5o7CXnY1Unq3J6oEIj1Hy 42wkU130 assertion
type: Assertion
description: [Genetic polymorphisms in nitric oxide synthase genes modify the relationship between vegetable and fruit intake and risk of 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/19423521
was generated by: ECO_0000203

NP66016.RAU-P501FnB0Dp-eI Smul02vfoPWwy3eE3ZA51M2dzBM
has assertion: NP66016.RAU-P501FnB0Dp-eI Smul02vfoPWwy3eE3ZA51M2dzBM130 assertion
has provenance: NP66016.RAU-P501FnB0Dp-eI Smul02vfoPWwy3eE3ZA51M2dzBM130 provenance
has publication info: NP66016.RAU-P501FnB0Dp-eI Smul02vfoPWwy3eE3ZA51M2dzBM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66016.RAU-P501FnB0Dp-eI Smul02vfoPWwy3eE3ZA51M2dzBM130 assertion
type: Assertion
description: [Endothelial nitric oxide synthase gene polymorphisms in patients with nontraumatic femoral head osteonecrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16779830
was generated by: ECO_0000203

NP66020.RAdoA -X1Yvf1pPowz0z18I FjwK5AvPt sAb3y JU5Dg
has assertion: NP66020.RAdoA -X1Yvf1pPowz0z18I FjwK5AvPt sAb3y JU5Dg130 assertion
has provenance: NP66020.RAdoA -X1Yvf1pPowz0z18I FjwK5AvPt sAb3y JU5Dg130 provenance
has publication info: NP66020.RAdoA -X1Yvf1pPowz0z18I FjwK5AvPt sAb3y JU5Dg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66020.RAdoA -X1Yvf1pPowz0z18I FjwK5AvPt sAb3y JU5Dg130 assertion
type: Assertion
description: [Effect modification by smoking on the association between genetic polymorphisms in oxidative stress genes and colorectal 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/19622717
was generated by: ECO_0000203

NP66023.RAbCw4ra6tio6-5hHkc1UrIa1FiQKnVgBGJR73U7KU1 U
has assertion: NP66023.RAbCw4ra6tio6-5hHkc1UrIa1FiQKnVgBGJR73U7KU1 U130 assertion
has provenance: NP66023.RAbCw4ra6tio6-5hHkc1UrIa1FiQKnVgBGJR73U7KU1 U130 provenance
has publication info: NP66023.RAbCw4ra6tio6-5hHkc1UrIa1FiQKnVgBGJR73U7KU1 U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66023.RAbCw4ra6tio6-5hHkc1UrIa1FiQKnVgBGJR73U7KU1 U130 assertion
type: Assertion
description: []. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16964084
was generated by: ECO_0000203

NP66026.RAYrdMJMgtSNvp0ev-JGPrP5hokvQPiELGysgwt60G31s
has assertion: NP66026.RAYrdMJMgtSNvp0ev-JGPrP5hokvQPiELGysgwt60G31s130 assertion
has provenance: NP66026.RAYrdMJMgtSNvp0ev-JGPrP5hokvQPiELGysgwt60G31s130 provenance
has publication info: NP66026.RAYrdMJMgtSNvp0ev-JGPrP5hokvQPiELGysgwt60G31s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66026.RAYrdMJMgtSNvp0ev-JGPrP5hokvQPiELGysgwt60G31s130 assertion
type: Assertion
description: [The finding of eNOS T-786C SNP could be used to significantly differentiate between the presence and severity of cerebral vasospasm (p = 0.04).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17029342
was generated by: ECO_0000203

NP66038.RARYO1JOXvimMaAHB ze0 B KpeT9DiuK6rt-FreFbDM
has assertion: NP66038.RARYO1JOXvimMaAHB ze0 B KpeT9DiuK6rt-FreFbDM130 assertion
has provenance: NP66038.RARYO1JOXvimMaAHB ze0 B KpeT9DiuK6rt-FreFbDM130 provenance
has publication info: NP66038.RARYO1JOXvimMaAHB ze0 B KpeT9DiuK6rt-FreFbDM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66038.RARYO1JOXvimMaAHB ze0 B KpeT9DiuK6rt-FreFbDM130 assertion
type: Assertion
description: [NOTCH signaling pathway is essential in T-cell development and NOTCH1 mutations are frequently present in T-cell acute lymphoblastic leukemia (T-ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16707600
was generated by: ECO_0000203

NP66043.RAUFSHNxm6qGwMZCmqfC86dSD68J3P bS3FsuCjyF2Bjc
has assertion: NP66043.RAUFSHNxm6qGwMZCmqfC86dSD68J3P bS3FsuCjyF2Bjc130 assertion
has provenance: NP66043.RAUFSHNxm6qGwMZCmqfC86dSD68J3P bS3FsuCjyF2Bjc130 provenance
has publication info: NP66043.RAUFSHNxm6qGwMZCmqfC86dSD68J3P bS3FsuCjyF2Bjc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66043.RAUFSHNxm6qGwMZCmqfC86dSD68J3P bS3FsuCjyF2Bjc130 assertion
type: Assertion
description: [In this population-based case control study (n = 455 cases; 527 controls), we examined the only identified nonsynonymous polymorphism (Ala394Thr; rs2305160) in the largest circadian gene, neuronal PAS domain protein 2 (NPAS2), in order to examine its impact on NHL 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/17096334
was generated by: ECO_0000203

NP66048.RATywdTD6rlWU6LN6TjiaENBoMpBaWcKG9LSN3ZtquHyY
has assertion: NP66048.RATywdTD6rlWU6LN6TjiaENBoMpBaWcKG9LSN3ZtquHyY130 assertion
has provenance: NP66048.RATywdTD6rlWU6LN6TjiaENBoMpBaWcKG9LSN3ZtquHyY130 provenance
has publication info: NP66048.RATywdTD6rlWU6LN6TjiaENBoMpBaWcKG9LSN3ZtquHyY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66048.RATywdTD6rlWU6LN6TjiaENBoMpBaWcKG9LSN3ZtquHyY130 assertion
type: Assertion
description: [The genes HMGCS2, FDPS, RAFTLIN, ACAD8, NPC2, and ABCG1 were associated with AD at a significance level of P < or = 0.05 in this 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/17387528
was generated by: ECO_0000203

NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw
has assertion: NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130 assertion
has provenance: NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130 provenance
has publication info: NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130 assertion
type: Assertion
description: [The results demonstrate that NPHS1 and NPHS2 mutations are also present in Chinese sporadic NS patients, suggesting that genetic changes of nephrin and podocin may play pathogenetic roles in some patients with sporadic steroid resistant NS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17211152
was generated by: ECO_0000203

NP66062.RAUj1kYZKdw-GISae-B8c 4k4UdjQU5qS4SmJn7PcNE4w
has assertion: NP66062.RAUj1kYZKdw-GISae-B8c 4k4UdjQU5qS4SmJn7PcNE4w130 assertion
has provenance: NP66062.RAUj1kYZKdw-GISae-B8c 4k4UdjQU5qS4SmJn7PcNE4w130 provenance
has publication info: NP66062.RAUj1kYZKdw-GISae-B8c 4k4UdjQU5qS4SmJn7PcNE4w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66062.RAUj1kYZKdw-GISae-B8c 4k4UdjQU5qS4SmJn7PcNE4w130 assertion
type: Assertion
description: [Our results do suggest that variants of the ANF gene might be involved in the determination of left ventricular hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17259761
was generated by: ECO_0000203

NP66067.RAXsVuXOCcpElyezNi8nTUccb9em -ANWDF9rH7G9KFow
has assertion: NP66067.RAXsVuXOCcpElyezNi8nTUccb9em -ANWDF9rH7G9KFow130 assertion
has provenance: NP66067.RAXsVuXOCcpElyezNi8nTUccb9em -ANWDF9rH7G9KFow130 provenance
has publication info: NP66067.RAXsVuXOCcpElyezNi8nTUccb9em -ANWDF9rH7G9KFow130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66067.RAXsVuXOCcpElyezNi8nTUccb9em -ANWDF9rH7G9KFow130 assertion
type: Assertion
description: [This study provides further evidence for an effect of NPSR1 on asthma, atopy and 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/19996348
was generated by: ECO_0000203

NP66068.RAU azgxiDXNud8napIjJ-UD419CCFo6mvy56IWUPo4mI
has assertion: NP66068.RAU azgxiDXNud8napIjJ-UD419CCFo6mvy56IWUPo4mI130 assertion
has provenance: NP66068.RAU azgxiDXNud8napIjJ-UD419CCFo6mvy56IWUPo4mI130 provenance
has publication info: NP66068.RAU azgxiDXNud8napIjJ-UD419CCFo6mvy56IWUPo4mI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66068.RAU azgxiDXNud8napIjJ-UD419CCFo6mvy56IWUPo4mI130 assertion
type: Assertion
description: [For ADAM33, NPSR1, and CYFIP2, the associations with asthma or asthma-related phenotypes have been studied in East Asian populations such as Chinese and Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19951440
was generated by: ECO_0000203

NP66069.RARxnmULNm6owLRJ28-tLE3HYEFBmEp9elhlyBC8Vd7dU
has assertion: NP66069.RARxnmULNm6owLRJ28-tLE3HYEFBmEp9elhlyBC8Vd7dU130 assertion
has provenance: NP66069.RARxnmULNm6owLRJ28-tLE3HYEFBmEp9elhlyBC8Vd7dU130 provenance
has publication info: NP66069.RARxnmULNm6owLRJ28-tLE3HYEFBmEp9elhlyBC8Vd7dU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66069.RARxnmULNm6owLRJ28-tLE3HYEFBmEp9elhlyBC8Vd7dU130 assertion
type: Assertion
description: [To analyze the association of G protein-coupled receptor 154 with asthma and total and mite-specific IgE levels in a population of the Caribbean Coast of Colombia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19624525
was generated by: ECO_0000203

NP66072.RAQAeYPdKGEp9xew3kNgMKWs KX6NJcJoTLJMLFEDCUyQ
has assertion: NP66072.RAQAeYPdKGEp9xew3kNgMKWs KX6NJcJoTLJMLFEDCUyQ130 assertion
has provenance: NP66072.RAQAeYPdKGEp9xew3kNgMKWs KX6NJcJoTLJMLFEDCUyQ130 provenance
has publication info: NP66072.RAQAeYPdKGEp9xew3kNgMKWs KX6NJcJoTLJMLFEDCUyQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66072.RAQAeYPdKGEp9xew3kNgMKWs KX6NJcJoTLJMLFEDCUyQ130 assertion
type: Assertion
description: [Common variants rs12649641, rs2342676 and rs6857530 in the 5' region of NPY2R are associated with obesity in Danish white 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/17019604
was generated by: ECO_0000203

NP66075.RAY9 4gwO7u5LSQs1YnA6pFGRGeNDfNnFvPSrdS38g0iU
has assertion: NP66075.RAY9 4gwO7u5LSQs1YnA6pFGRGeNDfNnFvPSrdS38g0iU130 assertion
has provenance: NP66075.RAY9 4gwO7u5LSQs1YnA6pFGRGeNDfNnFvPSrdS38g0iU130 provenance
has publication info: NP66075.RAY9 4gwO7u5LSQs1YnA6pFGRGeNDfNnFvPSrdS38g0iU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66075.RAY9 4gwO7u5LSQs1YnA6pFGRGeNDfNnFvPSrdS38g0iU130 assertion
type: Assertion
description: [Associations between obesity-related phenotypes and four genes in these pathways - leptin (LEP), leptin receptor (LEPR), neuropeptide Y2 receptor (NPY2R) and peptide YY (PYY) were examined in CARDIA Study participants (aged 18-30 at recruitment in 1985-6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20642810
was generated by: ECO_0000203

NP66077.RAfNb-rlhfm7aAI-CP9b5ktl-i9LJxTYsGH2OqReeOAYg
has assertion: NP66077.RAfNb-rlhfm7aAI-CP9b5ktl-i9LJxTYsGH2OqReeOAYg130 assertion
has provenance: NP66077.RAfNb-rlhfm7aAI-CP9b5ktl-i9LJxTYsGH2OqReeOAYg130 provenance
has publication info: NP66077.RAfNb-rlhfm7aAI-CP9b5ktl-i9LJxTYsGH2OqReeOAYg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66077.RAfNb-rlhfm7aAI-CP9b5ktl-i9LJxTYsGH2OqReeOAYg130 assertion
type: Assertion
description: [Association studies of BMI and type 2 diabetes in the neuropeptide Y pathway: a possible role for NPY2R as a candidate gene for type 2 diabetes in 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/17325259
was generated by: ECO_0000203

NP66084.RAQYagbAFNvAPrAZYBo7rqd8KWtakZ z4HP b2I2Qc0yM
has assertion: NP66084.RAQYagbAFNvAPrAZYBo7rqd8KWtakZ z4HP b2I2Qc0yM130 assertion
has provenance: NP66084.RAQYagbAFNvAPrAZYBo7rqd8KWtakZ z4HP b2I2Qc0yM130 provenance
has publication info: NP66084.RAQYagbAFNvAPrAZYBo7rqd8KWtakZ z4HP b2I2Qc0yM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66084.RAQYagbAFNvAPrAZYBo7rqd8KWtakZ z4HP b2I2Qc0yM130 assertion
type: Assertion
description: [Polymorphisms of drug-metabolizing genes and risk of 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/19899130
was generated by: ECO_0000203

NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY
has assertion: NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130 assertion
has provenance: NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130 provenance
has publication info: NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130 assertion
type: Assertion
description: [our data suggested that CYP1B1 germ line-inactivating mutations might increase the incidence of HCA in women with HNF1alpha 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/17363580
was generated by: ECO_0000203

NP66088.RAQsKVCKy0P393bEH3FW1y jvu3X6IDxt2aLSi0tGNSrc
has assertion: NP66088.RAQsKVCKy0P393bEH3FW1y jvu3X6IDxt2aLSi0tGNSrc130 assertion
has provenance: NP66088.RAQsKVCKy0P393bEH3FW1y jvu3X6IDxt2aLSi0tGNSrc130 provenance
has publication info: NP66088.RAQsKVCKy0P393bEH3FW1y jvu3X6IDxt2aLSi0tGNSrc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66088.RAQsKVCKy0P393bEH3FW1y jvu3X6IDxt2aLSi0tGNSrc130 assertion
type: Assertion
description: [The results of our study of Turkish prostate cancer patients suggests that mutation of the NQO1 gene may effect the serum PSA and alkaline phosphatase 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/18225579
was generated by: ECO_0000203

NP66089.RAQY48oSy-Kxf-Oerd61qmE1UR0RQ4F419J8vRDc2DOoU
has assertion: NP66089.RAQY48oSy-Kxf-Oerd61qmE1UR0RQ4F419J8vRDc2DOoU130 assertion
has provenance: NP66089.RAQY48oSy-Kxf-Oerd61qmE1UR0RQ4F419J8vRDc2DOoU130 provenance
has publication info: NP66089.RAQY48oSy-Kxf-Oerd61qmE1UR0RQ4F419J8vRDc2DOoU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66089.RAQY48oSy-Kxf-Oerd61qmE1UR0RQ4F419J8vRDc2DOoU130 assertion
type: Assertion
description: [These results show that genetic variation in the PXR encoding gene, which has been associated with altered activity of PXR, is strongly associated with susceptibility to IBD, CD, and UC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16472590
was generated by: ECO_0000203

NP66100.RAWfPgRFayi-C6M-soIsFKtcT5F5tZTNilJnzW-f18lSw
has assertion: NP66100.RAWfPgRFayi-C6M-soIsFKtcT5F5tZTNilJnzW-f18lSw130 assertion
has provenance: NP66100.RAWfPgRFayi-C6M-soIsFKtcT5F5tZTNilJnzW-f18lSw130 provenance
has publication info: NP66100.RAWfPgRFayi-C6M-soIsFKtcT5F5tZTNilJnzW-f18lSw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66100.RAWfPgRFayi-C6M-soIsFKtcT5F5tZTNilJnzW-f18lSw130 assertion
type: Assertion
description: [These new findings suggest that observed associations between NRG1 and schizophrenia may be mediated through functional interaction not just with ERBB4, but with other members of the NRG and ERBB 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/17598910
was generated by: ECO_0000203

NP66101.RARzr54uQxjq7MlD NxeS-mreM2uY7EjIHMmz s8pcv-g
has assertion: NP66101.RARzr54uQxjq7MlD NxeS-mreM2uY7EjIHMmz s8pcv-g130 assertion
has provenance: NP66101.RARzr54uQxjq7MlD NxeS-mreM2uY7EjIHMmz s8pcv-g130 provenance
has publication info: NP66101.RARzr54uQxjq7MlD NxeS-mreM2uY7EjIHMmz s8pcv-g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66101.RARzr54uQxjq7MlD NxeS-mreM2uY7EjIHMmz s8pcv-g130 assertion
type: Assertion
description: [The result supports that the NRG3 gene is a susceptibility gene 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/18708184
was generated by: ECO_0000203

NP66109.RAXgYaB5dRNKTzsL3jRfvgO7bBKvCVwmO9KpA n6vW6WQ
has assertion: NP66109.RAXgYaB5dRNKTzsL3jRfvgO7bBKvCVwmO9KpA n6vW6WQ130 assertion
has provenance: NP66109.RAXgYaB5dRNKTzsL3jRfvgO7bBKvCVwmO9KpA n6vW6WQ130 provenance
has publication info: NP66109.RAXgYaB5dRNKTzsL3jRfvgO7bBKvCVwmO9KpA n6vW6WQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66109.RAXgYaB5dRNKTzsL3jRfvgO7bBKvCVwmO9KpA n6vW6WQ130 assertion
type: Assertion
description: [Association of polymorphisms in the MTH1 gene with small cell lung carcinoma 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/16774934
was generated by: ECO_0000203

NP66110.RAU7nLPuWm9jvVcxPSundefmaULRQ6SnOIUdvR96upvVQ
has assertion: NP66110.RAU7nLPuWm9jvVcxPSundefmaULRQ6SnOIUdvR96upvVQ130 assertion
has provenance: NP66110.RAU7nLPuWm9jvVcxPSundefmaULRQ6SnOIUdvR96upvVQ130 provenance
has publication info: NP66110.RAU7nLPuWm9jvVcxPSundefmaULRQ6SnOIUdvR96upvVQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66110.RAU7nLPuWm9jvVcxPSundefmaULRQ6SnOIUdvR96upvVQ130 assertion
type: Assertion
description: [The observations suggest that NYX may have independent effects on myopia and night blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17392683
was generated by: ECO_0000203

NP66111.RAX7zRtALkD5qyI1JJLf6yHcWTiRKfz9EWHjJ7STWau6k
has assertion: NP66111.RAX7zRtALkD5qyI1JJLf6yHcWTiRKfz9EWHjJ7STWau6k130 assertion
has provenance: NP66111.RAX7zRtALkD5qyI1JJLf6yHcWTiRKfz9EWHjJ7STWau6k130 provenance
has publication info: NP66111.RAX7zRtALkD5qyI1JJLf6yHcWTiRKfz9EWHjJ7STWau6k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66111.RAX7zRtALkD5qyI1JJLf6yHcWTiRKfz9EWHjJ7STWau6k130 assertion
type: Assertion
description: [Polymorphisms in oxidative stress genes and risk for 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/16543247
was generated by: ECO_0000203

NP66117.RATAjIqYaOZoabCFqyhCzjaEDdec- W7619TuSMstC52k
has assertion: NP66117.RATAjIqYaOZoabCFqyhCzjaEDdec- W7619TuSMstC52k130 assertion
has provenance: NP66117.RATAjIqYaOZoabCFqyhCzjaEDdec- W7619TuSMstC52k130 provenance
has publication info: NP66117.RATAjIqYaOZoabCFqyhCzjaEDdec- W7619TuSMstC52k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66117.RATAjIqYaOZoabCFqyhCzjaEDdec- W7619TuSMstC52k130 assertion
type: Assertion
description: [Rapid detection of the hOGG1 Ser326Cys polymorphism using LightCycler technology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18569589
was generated by: ECO_0000203

NP66118.RAYLAJMkX82oQLRxnrYDArLyGmfwJJ6DBUhEa0-ecA8os
has assertion: NP66118.RAYLAJMkX82oQLRxnrYDArLyGmfwJJ6DBUhEa0-ecA8os130 assertion
has provenance: NP66118.RAYLAJMkX82oQLRxnrYDArLyGmfwJJ6DBUhEa0-ecA8os130 provenance
has publication info: NP66118.RAYLAJMkX82oQLRxnrYDArLyGmfwJJ6DBUhEa0-ecA8os130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66118.RAYLAJMkX82oQLRxnrYDArLyGmfwJJ6DBUhEa0-ecA8os130 assertion
type: Assertion
description: [Association of hOGG1 genotype with life style and oxidative DNA damage among Chinese ethnic 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/19350226
was generated by: ECO_0000203

NP66119.RAfxFUd58369d5xVcZ4fk-tmk-fuxz9fBksxfxRHueCkQ
has assertion: NP66119.RAfxFUd58369d5xVcZ4fk-tmk-fuxz9fBksxfxRHueCkQ130 assertion
has provenance: NP66119.RAfxFUd58369d5xVcZ4fk-tmk-fuxz9fBksxfxRHueCkQ130 provenance
has publication info: NP66119.RAfxFUd58369d5xVcZ4fk-tmk-fuxz9fBksxfxRHueCkQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66119.RAfxFUd58369d5xVcZ4fk-tmk-fuxz9fBksxfxRHueCkQ130 assertion
type: Assertion
description: [Biomarkers of nucleic acid oxidation, polymorphism in, and expression of, hOGG1 gene in styrene-exposed workers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19563869
was generated by: ECO_0000203

NP66121.RAVBBKL7wgJeUwOZkMh0nI7Wu8xq3jxfvdVJXwgB ilt8
has assertion: NP66121.RAVBBKL7wgJeUwOZkMh0nI7Wu8xq3jxfvdVJXwgB ilt8130 assertion
has provenance: NP66121.RAVBBKL7wgJeUwOZkMh0nI7Wu8xq3jxfvdVJXwgB ilt8130 provenance
has publication info: NP66121.RAVBBKL7wgJeUwOZkMh0nI7Wu8xq3jxfvdVJXwgB ilt8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66121.RAVBBKL7wgJeUwOZkMh0nI7Wu8xq3jxfvdVJXwgB ilt8130 assertion
type: Assertion
description: [Oxidative damage to biological macromolecules in Prague bus drivers and garagemen: impact of air pollution and genetic 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/20723587
was generated by: ECO_0000203

NP66122.RAVzTFO2UhWUKBhb4qM0vcEJ4GvNRMPWLPq0CgMGtgeuI
has assertion: NP66122.RAVzTFO2UhWUKBhb4qM0vcEJ4GvNRMPWLPq0CgMGtgeuI130 assertion
has provenance: NP66122.RAVzTFO2UhWUKBhb4qM0vcEJ4GvNRMPWLPq0CgMGtgeuI130 provenance
has publication info: NP66122.RAVzTFO2UhWUKBhb4qM0vcEJ4GvNRMPWLPq0CgMGtgeuI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66122.RAVzTFO2UhWUKBhb4qM0vcEJ4GvNRMPWLPq0CgMGtgeuI130 assertion
type: Assertion
description: [hOGG1 SER326CYS genetic polymorphism 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/15834708
was generated by: ECO_0000203

NP66124.RAabutIILu8A2hB0tsKBcjGv49BNswWhtlXdJiSJT9GuY
has assertion: NP66124.RAabutIILu8A2hB0tsKBcjGv49BNswWhtlXdJiSJT9GuY130 assertion
has provenance: NP66124.RAabutIILu8A2hB0tsKBcjGv49BNswWhtlXdJiSJT9GuY130 provenance
has publication info: NP66124.RAabutIILu8A2hB0tsKBcjGv49BNswWhtlXdJiSJT9GuY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66124.RAabutIILu8A2hB0tsKBcjGv49BNswWhtlXdJiSJT9GuY130 assertion
type: Assertion
description: [Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to 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/16891421
was generated by: ECO_0000203

NP66125.RAfWbz yIadbjdP-EDrmmBDUX-ar5rEKuiHdPr1osrZvU
has assertion: NP66125.RAfWbz yIadbjdP-EDrmmBDUX-ar5rEKuiHdPr1osrZvU130 assertion
has provenance: NP66125.RAfWbz yIadbjdP-EDrmmBDUX-ar5rEKuiHdPr1osrZvU130 provenance
has publication info: NP66125.RAfWbz yIadbjdP-EDrmmBDUX-ar5rEKuiHdPr1osrZvU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66125.RAfWbz yIadbjdP-EDrmmBDUX-ar5rEKuiHdPr1osrZvU130 assertion
type: Assertion
description: [The 2',3'-cyclic nucleotide 3'-phosphodiesterase and oligodendrocyte lineage transcription factor 2 genes do not appear to be associated with schizophrenia 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/17010574
was generated by: ECO_0000203

NP66128.RATIZaUFfrQDR3UVUT3q5JvFFsUNTrymt3fjqQ1CWu8Cc
has assertion: NP66128.RATIZaUFfrQDR3UVUT3q5JvFFsUNTrymt3fjqQ1CWu8Cc130 assertion
has provenance: NP66128.RATIZaUFfrQDR3UVUT3q5JvFFsUNTrymt3fjqQ1CWu8Cc130 provenance
has publication info: NP66128.RATIZaUFfrQDR3UVUT3q5JvFFsUNTrymt3fjqQ1CWu8Cc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66128.RATIZaUFfrQDR3UVUT3q5JvFFsUNTrymt3fjqQ1CWu8Cc130 assertion
type: Assertion
description: [Association of the kappa-opioid system 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/16924269
was generated by: ECO_0000203

NP66130.RAYo1YyfK0ujZFFbPMCqDnjx4-F WI8IOs6bXURYZfsZ4
has assertion: NP66130.RAYo1YyfK0ujZFFbPMCqDnjx4-F WI8IOs6bXURYZfsZ4130 assertion
has provenance: NP66130.RAYo1YyfK0ujZFFbPMCqDnjx4-F WI8IOs6bXURYZfsZ4130 provenance
has publication info: NP66130.RAYo1YyfK0ujZFFbPMCqDnjx4-F WI8IOs6bXURYZfsZ4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66130.RAYo1YyfK0ujZFFbPMCqDnjx4-F WI8IOs6bXURYZfsZ4130 assertion
type: Assertion
description: [The frequency of the minor allele was significantly lower in the subjects with chronic pain when compared with the group with acute postoperative pain (0.079 versus 0.158; P = 0.009 by chi2 test).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17000822
was generated by: ECO_0000203

NP66133.RAYht2sMxNOQu3u67UA5QTcLZ7n-4I1 edgbLV2vfqGhQ
has assertion: NP66133.RAYht2sMxNOQu3u67UA5QTcLZ7n-4I1 edgbLV2vfqGhQ130 assertion
has provenance: NP66133.RAYht2sMxNOQu3u67UA5QTcLZ7n-4I1 edgbLV2vfqGhQ130 provenance
has publication info: NP66133.RAYht2sMxNOQu3u67UA5QTcLZ7n-4I1 edgbLV2vfqGhQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66133.RAYht2sMxNOQu3u67UA5QTcLZ7n-4I1 edgbLV2vfqGhQ130 assertion
type: Assertion
description: [Postoperative pain management following orthognathic surgery in consideration of individual differences--is the antinociceptive effect of fentanyl related to the genotype involving nucleotide at OPRM1?.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19764432
was generated by: ECO_0000203

NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY
has assertion: NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130 assertion
has provenance: NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130 provenance
has publication info: NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66148.RAXPaFFLGpUCMu4wjhbvRWpBMgzeCWlAvh30NtGEFpFDY130 assertion
type: Assertion
description: [We investigated 29 single nucleotide polymorphisms (SNPs) within the P2RX7 gene and adjacent genes in a sample of 1000 German Caucasian patients suffering from recurrent major depressive disorder (MDD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16822851
was generated by: ECO_0000203

NP66151.RARrws2cHQdHEDt5zhs7B pVkUszx31uWmyyas PsDmjY
has assertion: NP66151.RARrws2cHQdHEDt5zhs7B pVkUszx31uWmyyas PsDmjY130 assertion
has provenance: NP66151.RARrws2cHQdHEDt5zhs7B pVkUszx31uWmyyas PsDmjY130 provenance
has publication info: NP66151.RARrws2cHQdHEDt5zhs7B pVkUszx31uWmyyas PsDmjY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66151.RARrws2cHQdHEDt5zhs7B pVkUszx31uWmyyas PsDmjY130 assertion
type: Assertion
description: [Increased risk of acute myocardial infarction and elevated levels of C-reactive protein in carriers of the Thr-87 variant of the ATP receptor P2Y11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17135283
was generated by: ECO_0000203

NP66152.RAWknVlN82kITVFkApNmcuVRaNxTBy1nSP apylxEs9Qw
has assertion: NP66152.RAWknVlN82kITVFkApNmcuVRaNxTBy1nSP apylxEs9Qw130 assertion
has provenance: NP66152.RAWknVlN82kITVFkApNmcuVRaNxTBy1nSP apylxEs9Qw130 provenance
has publication info: NP66152.RAWknVlN82kITVFkApNmcuVRaNxTBy1nSP apylxEs9Qw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66152.RAWknVlN82kITVFkApNmcuVRaNxTBy1nSP apylxEs9Qw130 assertion
type: Assertion
description: [PADI4 gene in multiple sclerosis: a family-based 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/16828881
was generated by: ECO_0000203

NP66165.RAU6f-MkU OhtL2BbHIE f7fWXNoR3kvI6Vr Etrfav6I
has assertion: NP66165.RAU6f-MkU OhtL2BbHIE f7fWXNoR3kvI6Vr Etrfav6I130 assertion
has provenance: NP66165.RAU6f-MkU OhtL2BbHIE f7fWXNoR3kvI6Vr Etrfav6I130 provenance
has publication info: NP66165.RAU6f-MkU OhtL2BbHIE f7fWXNoR3kvI6Vr Etrfav6I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66165.RAU6f-MkU OhtL2BbHIE f7fWXNoR3kvI6Vr Etrfav6I130 assertion
type: Assertion
description: [The ADPRT and XRCC1 polymorphisms confer host susceptibility to GCA, which might result from reduced ADPRT-XRCC1 interaction and attenuated base excision repair capacity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16890595
was generated by: ECO_0000203

NP66170.RAd2 4VkzCRFzJGI7SAZ0YWtHcSrOSfNOiEQCFPfF5JRg
has assertion: NP66170.RAd2 4VkzCRFzJGI7SAZ0YWtHcSrOSfNOiEQCFPfF5JRg130 assertion
has provenance: NP66170.RAd2 4VkzCRFzJGI7SAZ0YWtHcSrOSfNOiEQCFPfF5JRg130 provenance
has publication info: NP66170.RAd2 4VkzCRFzJGI7SAZ0YWtHcSrOSfNOiEQCFPfF5JRg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66170.RAd2 4VkzCRFzJGI7SAZ0YWtHcSrOSfNOiEQCFPfF5JRg130 assertion
type: Assertion
description: [We investigated whether polymorphisms at the visfatin/PBEF locus influence the risk of 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/17189536
was generated by: ECO_0000203

NP66174.RAX5RtTpJ1Zin5r22TdooypwUGte08kmY-zD-VtRssnG0
has assertion: NP66174.RAX5RtTpJ1Zin5r22TdooypwUGte08kmY-zD-VtRssnG0130 assertion
has provenance: NP66174.RAX5RtTpJ1Zin5r22TdooypwUGte08kmY-zD-VtRssnG0130 provenance
has publication info: NP66174.RAX5RtTpJ1Zin5r22TdooypwUGte08kmY-zD-VtRssnG0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66174.RAX5RtTpJ1Zin5r22TdooypwUGte08kmY-zD-VtRssnG0130 assertion
type: Assertion
description: [were also negative when the quantitative traits of weight and BMI were tested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20451405
was generated by: ECO_0000203

NP66179.RAQUBpAqPxMJrwvLAoxVp0AOX383ZhMn gFMHdI1QZZSs
has assertion: NP66179.RAQUBpAqPxMJrwvLAoxVp0AOX383ZhMn gFMHdI1QZZSs130 assertion
has provenance: NP66179.RAQUBpAqPxMJrwvLAoxVp0AOX383ZhMn gFMHdI1QZZSs130 provenance
has publication info: NP66179.RAQUBpAqPxMJrwvLAoxVp0AOX383ZhMn gFMHdI1QZZSs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66179.RAQUBpAqPxMJrwvLAoxVp0AOX383ZhMn gFMHdI1QZZSs130 assertion
type: Assertion
description: [Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to 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/16894060
was generated by: ECO_0000203

NP66187.RAaOtuu4iuxk7Qm01lAy192 84zdUrEfXC4cuIltUQ7jw
has assertion: NP66187.RAaOtuu4iuxk7Qm01lAy192 84zdUrEfXC4cuIltUQ7jw130 assertion
has provenance: NP66187.RAaOtuu4iuxk7Qm01lAy192 84zdUrEfXC4cuIltUQ7jw130 provenance
has publication info: NP66187.RAaOtuu4iuxk7Qm01lAy192 84zdUrEfXC4cuIltUQ7jw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66187.RAaOtuu4iuxk7Qm01lAy192 84zdUrEfXC4cuIltUQ7jw130 assertion
type: Assertion
description: [Programmed cell death 1 gene polymorphisms is associated with ankylosing spondylitis in 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/20012629
was generated by: ECO_0000203

NP66192.RAXTAXTGrKfgQomXh1eXAiR2vBqk9oVskrp6kW3Duf76c
has assertion: NP66192.RAXTAXTGrKfgQomXh1eXAiR2vBqk9oVskrp6kW3Duf76c130 assertion
has provenance: NP66192.RAXTAXTGrKfgQomXh1eXAiR2vBqk9oVskrp6kW3Duf76c130 provenance
has publication info: NP66192.RAXTAXTGrKfgQomXh1eXAiR2vBqk9oVskrp6kW3Duf76c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66192.RAXTAXTGrKfgQomXh1eXAiR2vBqk9oVskrp6kW3Duf76c130 assertion
type: Assertion
description: [Thus, we found significant associations with both the diagnosis of MDD and remission in response to antidepressants with SNPs in the PDE11A 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/17008408
was generated by: ECO_0000203

NP66200.RAXl26kblkRbbdzCKmjup hdlF5K0Ny4TQwDHMwwR4ly8
has assertion: NP66200.RAXl26kblkRbbdzCKmjup hdlF5K0Ny4TQwDHMwwR4ly8130 assertion
has provenance: NP66200.RAXl26kblkRbbdzCKmjup hdlF5K0Ny4TQwDHMwwR4ly8130 provenance
has publication info: NP66200.RAXl26kblkRbbdzCKmjup hdlF5K0Ny4TQwDHMwwR4ly8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66200.RAXl26kblkRbbdzCKmjup hdlF5K0Ny4TQwDHMwwR4ly8130 assertion
type: Assertion
description: [Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing 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/17264841
was generated by: ECO_0000203

NP66201.RAdEMqCssz2rFwQ q0VhCMPr0JinV0sfmeszNxAuP1GIg
has assertion: NP66201.RAdEMqCssz2rFwQ q0VhCMPr0JinV0sfmeszNxAuP1GIg130 assertion
has provenance: NP66201.RAdEMqCssz2rFwQ q0VhCMPr0JinV0sfmeszNxAuP1GIg130 provenance
has publication info: NP66201.RAdEMqCssz2rFwQ q0VhCMPr0JinV0sfmeszNxAuP1GIg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66201.RAdEMqCssz2rFwQ q0VhCMPr0JinV0sfmeszNxAuP1GIg130 assertion
type: Assertion
description: [Human clock, PER1 and PER2 polymorphisms: lack of association with cocaine dependence susceptibility and cocaine-induced paranoia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17106427
was generated by: ECO_0000203

NP66204.RAX0I9o-QznFmp2uy173ms1q4VbiL9jzipb mmD1fBfaw
has assertion: NP66204.RAX0I9o-QznFmp2uy173ms1q4VbiL9jzipb mmD1fBfaw130 assertion
has provenance: NP66204.RAX0I9o-QznFmp2uy173ms1q4VbiL9jzipb mmD1fBfaw130 provenance
has publication info: NP66204.RAX0I9o-QznFmp2uy173ms1q4VbiL9jzipb mmD1fBfaw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66204.RAX0I9o-QznFmp2uy173ms1q4VbiL9jzipb mmD1fBfaw130 assertion
type: Assertion
description: [Our findings suggest that HTR5A gene could play an important role in the pathogenesis of bipolar disorder 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/19328558
was generated by: ECO_0000203

NP66208.RAafnGXrE5qYXwgHGfJQdYLtIHRu49sLdrWywN0zFU2ZA
has assertion: NP66208.RAafnGXrE5qYXwgHGfJQdYLtIHRu49sLdrWywN0zFU2ZA130 assertion
has provenance: NP66208.RAafnGXrE5qYXwgHGfJQdYLtIHRu49sLdrWywN0zFU2ZA130 provenance
has publication info: NP66208.RAafnGXrE5qYXwgHGfJQdYLtIHRu49sLdrWywN0zFU2ZA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66208.RAafnGXrE5qYXwgHGfJQdYLtIHRu49sLdrWywN0zFU2ZA130 assertion
type: Assertion
description: [Mutations of the KRAS, BRAF, and PIK3CA genes have been reported in colorectal cancer (CRC), associated with resistance to epidermal growth factor receptor (EGFR)-targeted monoclonal antibody 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/20652941
was generated by: ECO_0000203

NP66213.RAevPPYgBL1d6c32xK2g9GMIrQeksdvpuGQuImQkEotLo
has assertion: NP66213.RAevPPYgBL1d6c32xK2g9GMIrQeksdvpuGQuImQkEotLo130 assertion
has provenance: NP66213.RAevPPYgBL1d6c32xK2g9GMIrQeksdvpuGQuImQkEotLo130 provenance
has publication info: NP66213.RAevPPYgBL1d6c32xK2g9GMIrQeksdvpuGQuImQkEotLo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66213.RAevPPYgBL1d6c32xK2g9GMIrQeksdvpuGQuImQkEotLo130 assertion
type: Assertion
description: [BRAF genotype is correlated with PFS and OS in KRAS wild type mCRC patients, which is independent of cetuximab treatment. PIK3CA mutation, loss of PTEN expression, EGFR GCN and HER2 GCN have no predictive value for response to treatment with cetuximab, neither individually nor in combination with other markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20413299
was generated by: ECO_0000203

NP66215.RAa8dKaFhGCIB1hblI f76 BtHn6Lv6gbkzbikyj65zug
has assertion: NP66215.RAa8dKaFhGCIB1hblI f76 BtHn6Lv6gbkzbikyj65zug130 assertion
has provenance: NP66215.RAa8dKaFhGCIB1hblI f76 BtHn6Lv6gbkzbikyj65zug130 provenance
has publication info: NP66215.RAa8dKaFhGCIB1hblI f76 BtHn6Lv6gbkzbikyj65zug130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66215.RAa8dKaFhGCIB1hblI f76 BtHn6Lv6gbkzbikyj65zug130 assertion
type: Assertion
description: [ This study is one of the first comprehensive mutational analyses of major genes in a specific signaling pathway in a sizeable cohort of lung adenocarcinomas. Our results suggest the majority of gain-of-function mutations within kinase genes in the EGFR signaling pathway have already been identified. Our findings also implicate FGFR4 in the pathogenesis of a subset of lung adenocarcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17487277
was generated by: ECO_0000203

NP66221.RAVUm eANY3G7C1gXultGRVdoiX 6HysvVVxkyDxTH EU
has assertion: NP66221.RAVUm eANY3G7C1gXultGRVdoiX 6HysvVVxkyDxTH EU130 assertion
has provenance: NP66221.RAVUm eANY3G7C1gXultGRVdoiX 6HysvVVxkyDxTH EU130 provenance
has publication info: NP66221.RAVUm eANY3G7C1gXultGRVdoiX 6HysvVVxkyDxTH EU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66221.RAVUm eANY3G7C1gXultGRVdoiX 6HysvVVxkyDxTH EU130 assertion
type: Assertion
description: [Association study of NRG1, DTNBP1, RGS4, G72/G30, and PIP5K2A with schizophrenia and symptom severity in a Hungarian 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/19937977
was generated by: ECO_0000203

NP66229.RAdn-wQTNayEfx0GA GFIaTJwLzSAo1HaYBNnD0h eq9s
has assertion: NP66229.RAdn-wQTNayEfx0GA GFIaTJwLzSAo1HaYBNnD0h eq9s130 assertion
has provenance: NP66229.RAdn-wQTNayEfx0GA GFIaTJwLzSAo1HaYBNnD0h eq9s130 provenance
has publication info: NP66229.RAdn-wQTNayEfx0GA GFIaTJwLzSAo1HaYBNnD0h eq9s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66229.RAdn-wQTNayEfx0GA GFIaTJwLzSAo1HaYBNnD0h eq9s130 assertion
type: Assertion
description: [There was a significant difference in the frequency distribution of the urokinase gene 3-UTR C/T polymorphism in bladder cancer patients as compared to the normal control group (p < 0.05), but no significant difference in allelic frequencies or in carriage rates between bladder cancer patients and normal controls were observed. Our study suggests that uroki]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16825821
was generated by: ECO_0000203

NP66233.RAUE0wj7frDHJefT51vnKkXm1NKQBlzjXv2zjC8jmMtAs
has assertion: NP66233.RAUE0wj7frDHJefT51vnKkXm1NKQBlzjXv2zjC8jmMtAs130 assertion
has provenance: NP66233.RAUE0wj7frDHJefT51vnKkXm1NKQBlzjXv2zjC8jmMtAs130 provenance
has publication info: NP66233.RAUE0wj7frDHJefT51vnKkXm1NKQBlzjXv2zjC8jmMtAs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66233.RAUE0wj7frDHJefT51vnKkXm1NKQBlzjXv2zjC8jmMtAs130 assertion
type: Assertion
description: [TagSNP evaluation for the association of 42 inflammation loci and vascular disease: evidence of IL6, FGB, ALOX5, NFKBIA, and IL4R loci effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17115186
was generated by: ECO_0000203

NP66234.RAcRvFeu1QDQwgPSP0c-xGf27cLIzJ0dZVCpdsLv49xrE
has assertion: NP66234.RAcRvFeu1QDQwgPSP0c-xGf27cLIzJ0dZVCpdsLv49xrE130 assertion
has provenance: NP66234.RAcRvFeu1QDQwgPSP0c-xGf27cLIzJ0dZVCpdsLv49xrE130 provenance
has publication info: NP66234.RAcRvFeu1QDQwgPSP0c-xGf27cLIzJ0dZVCpdsLv49xrE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66234.RAcRvFeu1QDQwgPSP0c-xGf27cLIzJ0dZVCpdsLv49xrE130 assertion
type: Assertion
description: [PLP1 and GPM6B intragenic copy number analysis by MAPH in 262 patients with hypomyelinating leukodystrophies: Identification of one partial triplication and two partial deletions of PLP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16416265
was generated by: ECO_0000203

NP66237.RAQHpVCiEujOnCA2VCIP4CQVOCO9kAypffkaBMhoX4178
has assertion: NP66237.RAQHpVCiEujOnCA2VCIP4CQVOCO9kAypffkaBMhoX4178130 assertion
has provenance: NP66237.RAQHpVCiEujOnCA2VCIP4CQVOCO9kAypffkaBMhoX4178130 provenance
has publication info: NP66237.RAQHpVCiEujOnCA2VCIP4CQVOCO9kAypffkaBMhoX4178130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66237.RAQHpVCiEujOnCA2VCIP4CQVOCO9kAypffkaBMhoX4178130 assertion
type: Assertion
description: [Variation in the adiponutrin gene influences its expression and associates 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/16505250
was generated by: ECO_0000203

NP66240.RAecVDDiGnBTYpR2UgjV8Btfoezs2IDAGtN361LZZWyoo
has assertion: NP66240.RAecVDDiGnBTYpR2UgjV8Btfoezs2IDAGtN361LZZWyoo130 assertion
has provenance: NP66240.RAecVDDiGnBTYpR2UgjV8Btfoezs2IDAGtN361LZZWyoo130 provenance
has publication info: NP66240.RAecVDDiGnBTYpR2UgjV8Btfoezs2IDAGtN361LZZWyoo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66240.RAecVDDiGnBTYpR2UgjV8Btfoezs2IDAGtN361LZZWyoo130 assertion
type: Assertion
description: [The smallest region of allelic imbalance contains the podocalyxin-like (PODXL) gene, which we evaluate here as a candidate prostate cancer aggressiveness gene mapping to 7q32-q33.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16434482
was generated by: ECO_0000203

NP66241.RAVxOL9Hc6IeY7 yRcsP91l4SZkJ0ZKCcTxGrig0UrAMw
has assertion: NP66241.RAVxOL9Hc6IeY7 yRcsP91l4SZkJ0ZKCcTxGrig0UrAMw130 assertion
has provenance: NP66241.RAVxOL9Hc6IeY7 yRcsP91l4SZkJ0ZKCcTxGrig0UrAMw130 provenance
has publication info: NP66241.RAVxOL9Hc6IeY7 yRcsP91l4SZkJ0ZKCcTxGrig0UrAMw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66241.RAVxOL9Hc6IeY7 yRcsP91l4SZkJ0ZKCcTxGrig0UrAMw130 assertion
type: Assertion
description: [Polbeta may play a role in the breast carcinogenesis and the Lys289Met polymorphism of the polbeta gene may be considered as an independent, early, molecular diagnostic marker 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/17131038
was generated by: ECO_0000203

NP66243.RAfb4vmHHkGtrQ2GkY74PMVz9ulQOg6VAaczKhgmbtPpE
has assertion: NP66243.RAfb4vmHHkGtrQ2GkY74PMVz9ulQOg6VAaczKhgmbtPpE130 assertion
has provenance: NP66243.RAfb4vmHHkGtrQ2GkY74PMVz9ulQOg6VAaczKhgmbtPpE130 provenance
has publication info: NP66243.RAfb4vmHHkGtrQ2GkY74PMVz9ulQOg6VAaczKhgmbtPpE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66243.RAfb4vmHHkGtrQ2GkY74PMVz9ulQOg6VAaczKhgmbtPpE130 assertion
type: Assertion
description: [An intronic polymorphism associated with increased XRCC1 expression, reduced apoptosis and familial 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/16596326
was generated by: ECO_0000203

NP66248.RAa7ZwBIps-SCZN B4Vdsrwb7yyoDlgW6hKYCaluFpTEM
has assertion: NP66248.RAa7ZwBIps-SCZN B4Vdsrwb7yyoDlgW6hKYCaluFpTEM130 assertion
has provenance: NP66248.RAa7ZwBIps-SCZN B4Vdsrwb7yyoDlgW6hKYCaluFpTEM130 provenance
has publication info: NP66248.RAa7ZwBIps-SCZN B4Vdsrwb7yyoDlgW6hKYCaluFpTEM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66248.RAa7ZwBIps-SCZN B4Vdsrwb7yyoDlgW6hKYCaluFpTEM130 assertion
type: Assertion
description: [Genetic variation in base excision repair genes and the 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/17283177
was generated by: ECO_0000203

NP66251.RAcPpqoVsn-5gi2F23pZ0MIoSzILFVNzg4S53ZI9T1IL0
has assertion: NP66251.RAcPpqoVsn-5gi2F23pZ0MIoSzILFVNzg4S53ZI9T1IL0130 assertion
has provenance: NP66251.RAcPpqoVsn-5gi2F23pZ0MIoSzILFVNzg4S53ZI9T1IL0130 provenance
has publication info: NP66251.RAcPpqoVsn-5gi2F23pZ0MIoSzILFVNzg4S53ZI9T1IL0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66251.RAcPpqoVsn-5gi2F23pZ0MIoSzILFVNzg4S53ZI9T1IL0130 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

NP66253.RAasr18v-SIpMRGgCNnsJqX3DrvgTzc7ykOqHGfDuml-s
has assertion: NP66253.RAasr18v-SIpMRGgCNnsJqX3DrvgTzc7ykOqHGfDuml-s130 assertion
has provenance: NP66253.RAasr18v-SIpMRGgCNnsJqX3DrvgTzc7ykOqHGfDuml-s130 provenance
has publication info: NP66253.RAasr18v-SIpMRGgCNnsJqX3DrvgTzc7ykOqHGfDuml-s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66253.RAasr18v-SIpMRGgCNnsJqX3DrvgTzc7ykOqHGfDuml-s130 assertion
type: Assertion
description: [POLG1 in idiopathic Parkinson 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/16943369
was generated by: ECO_0000203

NP66255.RAdL0CRc 6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc
has assertion: NP66255.RAdL0CRc 6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130 assertion
has provenance: NP66255.RAdL0CRc 6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130 provenance
has publication info: NP66255.RAdL0CRc 6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66255.RAdL0CRc 6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130 assertion
type: Assertion
description: [This prompted us to carry out a detailed analysis of the coding region and intron-exon boundaries of POLG1 in Finnish patients with idiopathic sporadic Parkinson disease (PD) and in nonparkinsonian 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/17846414
was generated by: ECO_0000203

NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ Ls
has assertion: NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ Ls130 assertion
has provenance: NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ Ls130 provenance
has publication info: NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ Ls130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66259.RAQViamxkkx1itWa3i8Ow4mtNDY4evORvX0QqpAKLQ Ls130 assertion
type: Assertion
description: [The polymorphism of Glu298Asp eNOS gene in dead cases may be useful for determining the cause of death in CHD cases 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/16683402
was generated by: ECO_0000203

NP66260.RATdfR4yvzq22CZlosJVEfy2Rl4nlw6bj-80XbLxEI4XM
has assertion: NP66260.RATdfR4yvzq22CZlosJVEfy2Rl4nlw6bj-80XbLxEI4XM130 assertion
has provenance: NP66260.RATdfR4yvzq22CZlosJVEfy2Rl4nlw6bj-80XbLxEI4XM130 provenance
has publication info: NP66260.RATdfR4yvzq22CZlosJVEfy2Rl4nlw6bj-80XbLxEI4XM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66260.RATdfR4yvzq22CZlosJVEfy2Rl4nlw6bj-80XbLxEI4XM130 assertion
type: Assertion
description: [Association of polymorphisms in the paraoxonase 1 gene with breast cancer incidence in the CPS-II Nutrition Cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16775186
was generated by: ECO_0000203

NP66274.RASqogwrWvPbAREwK3QlZTpD9hEr6sO50wrmyJ2GPN01E
has assertion: NP66274.RASqogwrWvPbAREwK3QlZTpD9hEr6sO50wrmyJ2GPN01E130 assertion
has provenance: NP66274.RASqogwrWvPbAREwK3QlZTpD9hEr6sO50wrmyJ2GPN01E130 provenance
has publication info: NP66274.RASqogwrWvPbAREwK3QlZTpD9hEr6sO50wrmyJ2GPN01E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66274.RASqogwrWvPbAREwK3QlZTpD9hEr6sO50wrmyJ2GPN01E130 assertion
type: Assertion
description: [Polymorphisms in the KDR and POSTN genes: association with breast cancer susceptibility and 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/16807673
was generated by: ECO_0000203

NP66276.RAXuXxFZzex6L0MwBk2ZqfOcO7iSfExDVT-mrRypyyzUs
has assertion: NP66276.RAXuXxFZzex6L0MwBk2ZqfOcO7iSfExDVT-mrRypyyzUs130 assertion
has provenance: NP66276.RAXuXxFZzex6L0MwBk2ZqfOcO7iSfExDVT-mrRypyyzUs130 provenance
has publication info: NP66276.RAXuXxFZzex6L0MwBk2ZqfOcO7iSfExDVT-mrRypyyzUs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66276.RAXuXxFZzex6L0MwBk2ZqfOcO7iSfExDVT-mrRypyyzUs130 assertion
type: Assertion
description: [Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in 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/16934875
was generated by: ECO_0000203

NP66277.RAfCsN8U3spQI-apt4oLA NzJ4lDlnn44ecKetBLZbATs
has assertion: NP66277.RAfCsN8U3spQI-apt4oLA NzJ4lDlnn44ecKetBLZbATs130 assertion
has provenance: NP66277.RAfCsN8U3spQI-apt4oLA NzJ4lDlnn44ecKetBLZbATs130 provenance
has publication info: NP66277.RAfCsN8U3spQI-apt4oLA NzJ4lDlnn44ecKetBLZbATs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66277.RAfCsN8U3spQI-apt4oLA NzJ4lDlnn44ecKetBLZbATs130 assertion
type: Assertion
description: [Single nucleotide polymorphisms of PPARD in combination with the Gly482Ser substitution of PGC-1A and the Pro12Ala substitution of PPARG2 predict the conversion from impaired glucose tolerance to type 2 diabetes: the STOP-NIDDM trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16804087
was generated by: ECO_0000203

NP66284.RAazoXw8egLTMhwrhPLxwHhZdFTlc3U3AhFqVDDaibh-A
has assertion: NP66284.RAazoXw8egLTMhwrhPLxwHhZdFTlc3U3AhFqVDDaibh-A130 assertion
has provenance: NP66284.RAazoXw8egLTMhwrhPLxwHhZdFTlc3U3AhFqVDDaibh-A130 provenance
has publication info: NP66284.RAazoXw8egLTMhwrhPLxwHhZdFTlc3U3AhFqVDDaibh-A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66284.RAazoXw8egLTMhwrhPLxwHhZdFTlc3U3AhFqVDDaibh-A130 assertion
type: Assertion
description: [This study has shown that both Pro12Ala and His447His polymorphisms of PPAR-gamma are associated with PCOS 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/19549442
was generated by: ECO_0000203

NP66285.RAWgdsKibxM3QuHk3GuNEdjuqrKfNL71aiAkMF-ype1PE
has assertion: NP66285.RAWgdsKibxM3QuHk3GuNEdjuqrKfNL71aiAkMF-ype1PE130 assertion
has provenance: NP66285.RAWgdsKibxM3QuHk3GuNEdjuqrKfNL71aiAkMF-ype1PE130 provenance
has publication info: NP66285.RAWgdsKibxM3QuHk3GuNEdjuqrKfNL71aiAkMF-ype1PE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66285.RAWgdsKibxM3QuHk3GuNEdjuqrKfNL71aiAkMF-ype1PE130 assertion
type: Assertion
description: [The role of genetic variation in peroxisome proliferator-activated receptors in the polycystic ovary syndrome (PCOS): an original case-control study followed by systematic review and meta-analysis of existing evidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19681917
was generated by: ECO_0000203

NP66286.RAcX9HLwWZ1IkRutLp82j39dbKLhGkW2aqhsEks946GL8
has assertion: NP66286.RAcX9HLwWZ1IkRutLp82j39dbKLhGkW2aqhsEks946GL8130 assertion
has provenance: NP66286.RAcX9HLwWZ1IkRutLp82j39dbKLhGkW2aqhsEks946GL8130 provenance
has publication info: NP66286.RAcX9HLwWZ1IkRutLp82j39dbKLhGkW2aqhsEks946GL8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66286.RAcX9HLwWZ1IkRutLp82j39dbKLhGkW2aqhsEks946GL8130 assertion
type: Assertion
description: [A population-attributable risk of approximately 50% for the Pro12Pro genotype indicates that testing for the Pro12Ala of the PPARG gene in addition to the already identified clinical risk factors may become a useful tool to further reduce the risk of PPARgamma agonist-induced fluid retention and edema in patients with 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/16822823
was generated by: ECO_0000203

NP66292.RARj3Yt-BoKCMiqMj9W3CJLLpwl5yjMXpMUAWEBzBW-gc
has assertion: NP66292.RARj3Yt-BoKCMiqMj9W3CJLLpwl5yjMXpMUAWEBzBW-gc130 assertion
has provenance: NP66292.RARj3Yt-BoKCMiqMj9W3CJLLpwl5yjMXpMUAWEBzBW-gc130 provenance
has publication info: NP66292.RARj3Yt-BoKCMiqMj9W3CJLLpwl5yjMXpMUAWEBzBW-gc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66292.RARj3Yt-BoKCMiqMj9W3CJLLpwl5yjMXpMUAWEBzBW-gc130 assertion
type: Assertion
description: [Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial 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/16704985
was generated by: ECO_0000203

NP66310.RAW0ZSvHCB43PeU5CghFgNj6k-wS8SNtbEScfHcic9QB8
has assertion: NP66310.RAW0ZSvHCB43PeU5CghFgNj6k-wS8SNtbEScfHcic9QB8130 assertion
has provenance: NP66310.RAW0ZSvHCB43PeU5CghFgNj6k-wS8SNtbEScfHcic9QB8130 provenance
has publication info: NP66310.RAW0ZSvHCB43PeU5CghFgNj6k-wS8SNtbEScfHcic9QB8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66310.RAW0ZSvHCB43PeU5CghFgNj6k-wS8SNtbEScfHcic9QB8130 assertion
type: Assertion
description: [Germline mutations of the perforin gene are a frequent occurrence in childhood anaplastic large cell 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/17477373
was generated by: ECO_0000203

NP66312.RAVDXSdYXcH3r4EzTi8Gjlnuo84gH5Qmt8KvsolG5xTf0
has assertion: NP66312.RAVDXSdYXcH3r4EzTi8Gjlnuo84gH5Qmt8KvsolG5xTf0130 assertion
has provenance: NP66312.RAVDXSdYXcH3r4EzTi8Gjlnuo84gH5Qmt8KvsolG5xTf0130 provenance
has publication info: NP66312.RAVDXSdYXcH3r4EzTi8Gjlnuo84gH5Qmt8KvsolG5xTf0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66312.RAVDXSdYXcH3r4EzTi8Gjlnuo84gH5Qmt8KvsolG5xTf0130 assertion
type: Assertion
description: [We study the association between three protein kinase C, eta gene polymorphisms (+8134C/T, rs912620, rs959728), and susceptibility to 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/17957454
was generated by: ECO_0000203

NP66319.RAWDMOx6FkTHYDy-KL8BM700bWTOQLaLDbFa VaTudI0o
has assertion: NP66319.RAWDMOx6FkTHYDy-KL8BM700bWTOQLaLDbFa VaTudI0o130 assertion
has provenance: NP66319.RAWDMOx6FkTHYDy-KL8BM700bWTOQLaLDbFa VaTudI0o130 provenance
has publication info: NP66319.RAWDMOx6FkTHYDy-KL8BM700bWTOQLaLDbFa VaTudI0o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66319.RAWDMOx6FkTHYDy-KL8BM700bWTOQLaLDbFa VaTudI0o130 assertion
type: Assertion
description: [Prion protein gene codon 129 modulates clinical course of neurological Wilson 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/16543824
was generated by: ECO_0000203

NP66324.RAWa1XmJHlEXwQkec 59LuTuMwCKAJK1 9W0l RFva4Xk
has assertion: NP66324.RAWa1XmJHlEXwQkec 59LuTuMwCKAJK1 9W0l RFva4Xk130 assertion
has provenance: NP66324.RAWa1XmJHlEXwQkec 59LuTuMwCKAJK1 9W0l RFva4Xk130 provenance
has publication info: NP66324.RAWa1XmJHlEXwQkec 59LuTuMwCKAJK1 9W0l RFva4Xk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66324.RAWa1XmJHlEXwQkec 59LuTuMwCKAJK1 9W0l RFva4Xk130 assertion
type: Assertion
description: [TNF-alpha 308 G/A, PAI-1 4G/4G, and EPCR mutations influence the risk of severe sepsis 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/16444434
was generated by: ECO_0000203

NP66328.RAYxdOxBBzPKNFy8v3M1FUfX8YJF4F-vCl1 9oKLK-6J8
has assertion: NP66328.RAYxdOxBBzPKNFy8v3M1FUfX8YJF4F-vCl1 9oKLK-6J8130 assertion
has provenance: NP66328.RAYxdOxBBzPKNFy8v3M1FUfX8YJF4F-vCl1 9oKLK-6J8130 provenance
has publication info: NP66328.RAYxdOxBBzPKNFy8v3M1FUfX8YJF4F-vCl1 9oKLK-6J8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66328.RAYxdOxBBzPKNFy8v3M1FUfX8YJF4F-vCl1 9oKLK-6J8130 assertion
type: Assertion
description: [PRPF31 is one of four pre-mRNA splicing factors identified as causing autosomal dominant retinitis pigmentosa, with incomplete penetrance being the unique feature associated with mutations in this 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/17325180
was generated by: ECO_0000203

NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ
has assertion: NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130 assertion
has provenance: NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130 provenance
has publication info: NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130 assertion
type: Assertion
description: [Mutations in PRPF31, RHO, and PRPH2 were found in low frequencies (1 of 9 autosomal dominant RP families) in Chinese patients, and the PRPF31 and PRPH2 truncating mutations were novel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19506198
was generated by: ECO_0000203

NP66335.RAS8tPAH5r5chFKI7CAXCvUTvTaJoACv56BCUYBjsgEFk
has assertion: NP66335.RAS8tPAH5r5chFKI7CAXCvUTvTaJoACv56BCUYBjsgEFk130 assertion
has provenance: NP66335.RAS8tPAH5r5chFKI7CAXCvUTvTaJoACv56BCUYBjsgEFk130 provenance
has publication info: NP66335.RAS8tPAH5r5chFKI7CAXCvUTvTaJoACv56BCUYBjsgEFk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66335.RAS8tPAH5r5chFKI7CAXCvUTvTaJoACv56BCUYBjsgEFk130 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

NP66337.RAft3js1w9BMfmauq0sCV5TZx4frr5CoqqsVdmr3ENbMg
has assertion: NP66337.RAft3js1w9BMfmauq0sCV5TZx4frr5CoqqsVdmr3ENbMg130 assertion
has provenance: NP66337.RAft3js1w9BMfmauq0sCV5TZx4frr5CoqqsVdmr3ENbMg130 provenance
has publication info: NP66337.RAft3js1w9BMfmauq0sCV5TZx4frr5CoqqsVdmr3ENbMg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66337.RAft3js1w9BMfmauq0sCV5TZx4frr5CoqqsVdmr3ENbMg130 assertion
type: Assertion
description: [Our goal was to identify a potential contribution of the PSMD9 gene to type 2 diabetes in Italians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17516568
was generated by: ECO_0000203

NP66339.RASe7jEvEI 44LW8sKSFkTfHTN8Uis8wVLsAZoNBB1fz8
has assertion: NP66339.RASe7jEvEI 44LW8sKSFkTfHTN8Uis8wVLsAZoNBB1fz8130 assertion
has provenance: NP66339.RASe7jEvEI 44LW8sKSFkTfHTN8Uis8wVLsAZoNBB1fz8130 provenance
has publication info: NP66339.RASe7jEvEI 44LW8sKSFkTfHTN8Uis8wVLsAZoNBB1fz8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66339.RASe7jEvEI 44LW8sKSFkTfHTN8Uis8wVLsAZoNBB1fz8130 assertion
type: Assertion
description: [Polymorphisms in interleukin-15 gene on chromosome 4q31.2 are associated with psoriasis vulgaris 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/17554368
was generated by: ECO_0000203

NP66340.RAYnH2SuKxiIwyF2pn03tJbO6F7bxts7jiDpvKPhQxVFs
has assertion: NP66340.RAYnH2SuKxiIwyF2pn03tJbO6F7bxts7jiDpvKPhQxVFs130 assertion
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has publication info: NP66340.RAYnH2SuKxiIwyF2pn03tJbO6F7bxts7jiDpvKPhQxVFs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66340.RAYnH2SuKxiIwyF2pn03tJbO6F7bxts7jiDpvKPhQxVFs130 assertion
type: Assertion
description: [Autoinflammatory gene mutations in 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/17213252
was generated by: ECO_0000203

NP66341.RAU5o9lRNthCjT2T8oGoQMw1mSl0502jXut-zzgY4np6s
has assertion: NP66341.RAU5o9lRNthCjT2T8oGoQMw1mSl0502jXut-zzgY4np6s130 assertion
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has publication info: NP66341.RAU5o9lRNthCjT2T8oGoQMw1mSl0502jXut-zzgY4np6s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66341.RAU5o9lRNthCjT2T8oGoQMw1mSl0502jXut-zzgY4np6s130 assertion
type: Assertion
description: [The relationship between microsatellite instability and PTEN gene mutations in endometrial 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/16506206
was generated by: ECO_0000203

NP66347.RAZibG3jpSwgZRuvbO0KZr3YQ8FvX8iz3QXFrTATR QjA
has assertion: NP66347.RAZibG3jpSwgZRuvbO0KZr3YQ8FvX8iz3QXFrTATR QjA130 assertion
has provenance: NP66347.RAZibG3jpSwgZRuvbO0KZr3YQ8FvX8iz3QXFrTATR QjA130 provenance
has publication info: NP66347.RAZibG3jpSwgZRuvbO0KZr3YQ8FvX8iz3QXFrTATR QjA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66347.RAZibG3jpSwgZRuvbO0KZr3YQ8FvX8iz3QXFrTATR QjA130 assertion
type: Assertion
description: [Aspirin resistance in coronary artery disease is correlated to elevated markers for oxidative stress but not to the expression of cyclooxygenase (COX) 1/2, a novel COX-1 polymorphism or the PlA(1/2) 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/16702043
was generated by: ECO_0000203

NP66352.RAfpjz3KUcgpr4mLy5pu0Ak64aEzscFqxemuEPkwFYVC0
has assertion: NP66352.RAfpjz3KUcgpr4mLy5pu0Ak64aEzscFqxemuEPkwFYVC0130 assertion
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has publication info: NP66352.RAfpjz3KUcgpr4mLy5pu0Ak64aEzscFqxemuEPkwFYVC0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66352.RAfpjz3KUcgpr4mLy5pu0Ak64aEzscFqxemuEPkwFYVC0130 assertion
type: Assertion
description: [The COX-2 G/C -765 polymorphism may modulate the occurrence of cerebrovascular ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16479190
was generated by: ECO_0000203

NP66365.RAeBgck hg7nXGn5fRNiLIHL3VWzR12LfHdiGP9Q3VxqM
has assertion: NP66365.RAeBgck hg7nXGn5fRNiLIHL3VWzR12LfHdiGP9Q3VxqM130 assertion
has provenance: NP66365.RAeBgck hg7nXGn5fRNiLIHL3VWzR12LfHdiGP9Q3VxqM130 provenance
has publication info: NP66365.RAeBgck hg7nXGn5fRNiLIHL3VWzR12LfHdiGP9Q3VxqM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66365.RAeBgck hg7nXGn5fRNiLIHL3VWzR12LfHdiGP9Q3VxqM130 assertion
type: Assertion
description: [-765C carrier status should be considered as another susceptibility marker for gastric adenocarcinoma development in patients with atrophy or intestinal metaplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17006983
was generated by: ECO_0000203

NP66380.RATeV93SYwLiPVi2tjAo1HpygEqJ66TTsOSAZTbUP8yfY
has assertion: NP66380.RATeV93SYwLiPVi2tjAo1HpygEqJ66TTsOSAZTbUP8yfY130 assertion
has provenance: NP66380.RATeV93SYwLiPVi2tjAo1HpygEqJ66TTsOSAZTbUP8yfY130 provenance
has publication info: NP66380.RATeV93SYwLiPVi2tjAo1HpygEqJ66TTsOSAZTbUP8yfY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP66380.RATeV93SYwLiPVi2tjAo1HpygEqJ66TTsOSAZTbUP8yfY130 assertion
type: Assertion
description: [Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German 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/16339849
was generated by: ECO_0000203

NP66381.RAYDN-z3maH-2ttYHKKHYOU3enUnzwQ85YpWmZKYryEd4
has assertion: NP66381.RAYDN-z3maH-2ttYHKKHYOU3enUnzwQ85YpWmZKYryEd4130 assertion
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has publication info: NP66381.RAYDN-z3maH-2ttYHKKHYOU3enUnzwQ85YpWmZKYryEd4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66381.RAYDN-z3maH-2ttYHKKHYOU3enUnzwQ85YpWmZKYryEd4130 assertion
type: Assertion
description: [Association of functional variants of PTPN22 and tp53 in psoriatic 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/16507123
was generated by: ECO_0000203

NP66390.RAfH-NfmphosfrBwMX3p5cxjllupthXZByHYrv309bJOE
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has publication info: NP66390.RAfH-NfmphosfrBwMX3p5cxjllupthXZByHYrv309bJOE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66390.RAfH-NfmphosfrBwMX3p5cxjllupthXZByHYrv309bJOE130 assertion
type: Assertion
description: [A recent study has reported that MAGI1, MAGI2, and protein tyrosine phosphatase, receptor-type, Z polypeptide 1 (PTPRZ1; located on 7q31.3) gene products regulate the NRG1-ERBB4 signaling pathway, and PTPRZ1 is associated with schizophrenia in a Caucasian 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/18186075
was generated by: ECO_0000203

NP66392.RAVE-LG9FH4ASXD5N0EP 8eYbSJaHN0Qo71U-GevP3EeI
has assertion: NP66392.RAVE-LG9FH4ASXD5N0EP 8eYbSJaHN0Qo71U-GevP3EeI130 assertion
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has publication info: NP66392.RAVE-LG9FH4ASXD5N0EP 8eYbSJaHN0Qo71U-GevP3EeI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66392.RAVE-LG9FH4ASXD5N0EP 8eYbSJaHN0Qo71U-GevP3EeI130 assertion
type: Assertion
description: [We investigated whether putatively functional single nucleotide polymorphisms (SNPs) in genes related to CIN (CENPF, ESPL1, NEK2, PTTG1, ZWILCH, ZWINT) affect breast cancer (BC) risk and clinical outcome in a Swedish cohort of 749 incident BC cases with detailed clinical data and up to 15 years of follow-up and 1493 matched 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/19008095
was generated by: ECO_0000203

NP66393.RAaLkagVaFK1eM5umAkeJoFF2qv-VXDtrdhZCso44vDLg
has assertion: NP66393.RAaLkagVaFK1eM5umAkeJoFF2qv-VXDtrdhZCso44vDLg130 assertion
has provenance: NP66393.RAaLkagVaFK1eM5umAkeJoFF2qv-VXDtrdhZCso44vDLg130 provenance
has publication info: NP66393.RAaLkagVaFK1eM5umAkeJoFF2qv-VXDtrdhZCso44vDLg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66393.RAaLkagVaFK1eM5umAkeJoFF2qv-VXDtrdhZCso44vDLg130 assertion
type: Assertion
description: [Our findings support previous data showing that VDR SNPs modulate the risk for TB in West Africans and suggest that variation within DC-SIGN and PTX3 also affect the disease 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/17611589
was generated by: ECO_0000203

NP66395.RAX8EXAcqT4M6qqBUncP UJMoNGxM42Pz3MWYJnVlU7ow
has assertion: NP66395.RAX8EXAcqT4M6qqBUncP UJMoNGxM42Pz3MWYJnVlU7ow130 assertion
has provenance: NP66395.RAX8EXAcqT4M6qqBUncP UJMoNGxM42Pz3MWYJnVlU7ow130 provenance
has publication info: NP66395.RAX8EXAcqT4M6qqBUncP UJMoNGxM42Pz3MWYJnVlU7ow130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66395.RAX8EXAcqT4M6qqBUncP UJMoNGxM42Pz3MWYJnVlU7ow130 assertion
type: Assertion
description: [the analysis of a very large data set suggests that genetic polymorphisms in PVRL2 may influence MS severity and supports the possibility that viral factors may contribute to the clinical course of MS, consistent with previous reports.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16738668
was generated by: ECO_0000203

NP66404.RAfrQXVpBSiR 7ablUMJA3Wmp0qKjsRSy3QlVTZdutZk8
has assertion: NP66404.RAfrQXVpBSiR 7ablUMJA3Wmp0qKjsRSy3QlVTZdutZk8130 assertion
has provenance: NP66404.RAfrQXVpBSiR 7ablUMJA3Wmp0qKjsRSy3QlVTZdutZk8130 provenance
has publication info: NP66404.RAfrQXVpBSiR 7ablUMJA3Wmp0qKjsRSy3QlVTZdutZk8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66404.RAfrQXVpBSiR 7ablUMJA3Wmp0qKjsRSy3QlVTZdutZk8130 assertion
type: Assertion
description: [Some common mutations of RAD50 and NBS1 in western populations do not contribute significantly to Chinese non-BRCA1/2 hereditary 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/19904603
was generated by: ECO_0000203

NP66405.RAUPasmkVAfV5LLSFhPaA6qU0lCJAheVdO44556OqrXJQ
has assertion: NP66405.RAUPasmkVAfV5LLSFhPaA6qU0lCJAheVdO44556OqrXJQ130 assertion
has provenance: NP66405.RAUPasmkVAfV5LLSFhPaA6qU0lCJAheVdO44556OqrXJQ130 provenance
has publication info: NP66405.RAUPasmkVAfV5LLSFhPaA6qU0lCJAheVdO44556OqrXJQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66405.RAUPasmkVAfV5LLSFhPaA6qU0lCJAheVdO44556OqrXJQ130 assertion
type: Assertion
description: [Rad50 c.687delT does not contribute significantly to familial breast cancer in a 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/19190165
was generated by: ECO_0000203

NP66409.RAX6iBzS5Q7mpiO71bdDeQO5 bP lJ0XZ-5mIEeSTrrVs
has assertion: NP66409.RAX6iBzS5Q7mpiO71bdDeQO5 bP lJ0XZ-5mIEeSTrrVs130 assertion
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has publication info: NP66409.RAX6iBzS5Q7mpiO71bdDeQO5 bP lJ0XZ-5mIEeSTrrVs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66409.RAX6iBzS5Q7mpiO71bdDeQO5 bP lJ0XZ-5mIEeSTrrVs130 assertion
type: Assertion
description: [Comprehensive screen of genetic variation in DNA repair pathway genes and postmenopausal 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/20496165
was generated by: ECO_0000203

NP66421.RASccNTcAWKfV4-KAi22IgBP8MU7M4mc1gzrhg5ROc-dA
has assertion: NP66421.RASccNTcAWKfV4-KAi22IgBP8MU7M4mc1gzrhg5ROc-dA130 assertion
has provenance: NP66421.RASccNTcAWKfV4-KAi22IgBP8MU7M4mc1gzrhg5ROc-dA130 provenance
has publication info: NP66421.RASccNTcAWKfV4-KAi22IgBP8MU7M4mc1gzrhg5ROc-dA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66421.RASccNTcAWKfV4-KAi22IgBP8MU7M4mc1gzrhg5ROc-dA130 assertion
type: Assertion
description: [Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related 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/16857995
was generated by: ECO_0000203

NP66422.RAW7Af-RFn9mXKsmODyqgePS7K9evk9kiwMqCJAbivhzY
has assertion: NP66422.RAW7Af-RFn9mXKsmODyqgePS7K9evk9kiwMqCJAbivhzY130 assertion
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has publication info: NP66422.RAW7Af-RFn9mXKsmODyqgePS7K9evk9kiwMqCJAbivhzY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66422.RAW7Af-RFn9mXKsmODyqgePS7K9evk9kiwMqCJAbivhzY130 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

NP66423.RAcY1PuWrpuOHfTyfMhTUDrycn C9kr9IrYDHAtS64Jb0
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type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66423.RAcY1PuWrpuOHfTyfMhTUDrycn C9kr9IrYDHAtS64Jb0130 assertion
type: Assertion
description: [A combined effect of the KPNA3 and KPNB3 genes on susceptibility to 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/16644122
was generated by: ECO_0000203

NP66430.RAVkG8GAI76--CgToPYkTwFYaHDXF-mfvTWHMgALInuJA
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has provenance: NP66430.RAVkG8GAI76--CgToPYkTwFYaHDXF-mfvTWHMgALInuJA130 provenance
has publication info: NP66430.RAVkG8GAI76--CgToPYkTwFYaHDXF-mfvTWHMgALInuJA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66430.RAVkG8GAI76--CgToPYkTwFYaHDXF-mfvTWHMgALInuJA130 assertion
type: Assertion
description: [Significant effect of homologous recombination DNA repair gene polymorphisms on pancreatic cancer 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/16540687
was generated by: ECO_0000203

NP66434.RAf0hWnZyxuJHs aFfY1yXFQLCbxsMDHGLq2q6iBtlZf8
has assertion: NP66434.RAf0hWnZyxuJHs aFfY1yXFQLCbxsMDHGLq2q6iBtlZf8130 assertion
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has publication info: NP66434.RAf0hWnZyxuJHs aFfY1yXFQLCbxsMDHGLq2q6iBtlZf8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66434.RAf0hWnZyxuJHs aFfY1yXFQLCbxsMDHGLq2q6iBtlZf8130 assertion
type: Assertion
description: [Rgs 2 gene polymorphisms as modulators of anxiety in humans?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16736243
was generated by: ECO_0000203

NP66440.RAcJseFUwi42RV39rvGFKt7rBDSBvfng67EQUBD-ASY5Y
has assertion: NP66440.RAcJseFUwi42RV39rvGFKt7rBDSBvfng67EQUBD-ASY5Y130 assertion
has provenance: NP66440.RAcJseFUwi42RV39rvGFKt7rBDSBvfng67EQUBD-ASY5Y130 provenance
has publication info: NP66440.RAcJseFUwi42RV39rvGFKt7rBDSBvfng67EQUBD-ASY5Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66440.RAcJseFUwi42RV39rvGFKt7rBDSBvfng67EQUBD-ASY5Y130 assertion
type: Assertion
description: [The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17224235
was generated by: ECO_0000203

NP66443.RAYh4iZ8hGspS8aZ4e-KtzkO HyKrxWiBqqsqSj2Cg2Ms
has assertion: NP66443.RAYh4iZ8hGspS8aZ4e-KtzkO HyKrxWiBqqsqSj2Cg2Ms130 assertion
has provenance: NP66443.RAYh4iZ8hGspS8aZ4e-KtzkO HyKrxWiBqqsqSj2Cg2Ms130 provenance
has publication info: NP66443.RAYh4iZ8hGspS8aZ4e-KtzkO HyKrxWiBqqsqSj2Cg2Ms130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66443.RAYh4iZ8hGspS8aZ4e-KtzkO HyKrxWiBqqsqSj2Cg2Ms130 assertion
type: Assertion
description: [In an effort to identify additional gene polymorphisms in which variants have been implicated in asthma, we investigated the genetic polymorphisms in RUNX1 to evaluate it as a potential candidate gene for a host genetic study of asthma and IgE 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/17079875
was generated by: ECO_0000203

NP66447.RAWTXJtv35e6EsRkPSDqQyCxRmgDa9Po8cMxId70Ax8HA
has assertion: NP66447.RAWTXJtv35e6EsRkPSDqQyCxRmgDa9Po8cMxId70Ax8HA130 assertion
has provenance: NP66447.RAWTXJtv35e6EsRkPSDqQyCxRmgDa9Po8cMxId70Ax8HA130 provenance
has publication info: NP66447.RAWTXJtv35e6EsRkPSDqQyCxRmgDa9Po8cMxId70Ax8HA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66447.RAWTXJtv35e6EsRkPSDqQyCxRmgDa9Po8cMxId70Ax8HA130 assertion
type: Assertion
description: [The p11 protein (also called S100A10), which plays a pivotal role in the dynamic modulation of serotonergic 1B receptor function, has been implicated in the pathogenesis of major depressive disorder (MDD) and the therapeutic mechanisms of antidepressant 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/18838110
was generated by: ECO_0000203

NP66450.RAR2pWEDMmnVtk9hlNcjLDO7MlK3Ae-5nEnNmV-Rr1ac0
has assertion: NP66450.RAR2pWEDMmnVtk9hlNcjLDO7MlK3Ae-5nEnNmV-Rr1ac0130 assertion
has provenance: NP66450.RAR2pWEDMmnVtk9hlNcjLDO7MlK3Ae-5nEnNmV-Rr1ac0130 provenance
has publication info: NP66450.RAR2pWEDMmnVtk9hlNcjLDO7MlK3Ae-5nEnNmV-Rr1ac0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66450.RAR2pWEDMmnVtk9hlNcjLDO7MlK3Ae-5nEnNmV-Rr1ac0130 assertion
type: Assertion
description: [Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset 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/17373700
was generated by: ECO_0000203

NP66454.RAaJx9mXLPbvT7SqTiQ k7LBNm1izO x 5BPohtzrBEgk
has assertion: NP66454.RAaJx9mXLPbvT7SqTiQ k7LBNm1izO x 5BPohtzrBEgk130 assertion
has provenance: NP66454.RAaJx9mXLPbvT7SqTiQ k7LBNm1izO x 5BPohtzrBEgk130 provenance
has publication info: NP66454.RAaJx9mXLPbvT7SqTiQ k7LBNm1izO x 5BPohtzrBEgk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66454.RAaJx9mXLPbvT7SqTiQ k7LBNm1izO x 5BPohtzrBEgk130 assertion
type: Assertion
description: [The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17347258
was generated by: ECO_0000203

NP66458.RAadiuoCfqU75583chXwet7v9kw1c7soAXbRgO 29FGt8
has assertion: NP66458.RAadiuoCfqU75583chXwet7v9kw1c7soAXbRgO 29FGt8130 assertion
has provenance: NP66458.RAadiuoCfqU75583chXwet7v9kw1c7soAXbRgO 29FGt8130 provenance
has publication info: NP66458.RAadiuoCfqU75583chXwet7v9kw1c7soAXbRgO 29FGt8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66458.RAadiuoCfqU75583chXwet7v9kw1c7soAXbRgO 29FGt8130 assertion
type: Assertion
description: [The CFTR gene was first analyzed in all patients by denaturing high-performance liquid chromatography followed by direct sequencing; whereas, the sodium channel non-voltage-gated 1 alpha (SCNN1A), sodium channel non-voltage-gated 1 beta (SCNN1B), and sodium channel non-voltage-gated 1 gamma (SCNN1G) subunits of the ENaC gene were analyzed by sequencing in the five patients who carried only one CF 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/19017867
was generated by: ECO_0000203

NP66460.RAaOzdORfOJ2zdGgEsMO0Y tm74vu8cnKIxqu8rKvJ6F0
has assertion: NP66460.RAaOzdORfOJ2zdGgEsMO0Y tm74vu8cnKIxqu8rKvJ6F0130 assertion
has provenance: NP66460.RAaOzdORfOJ2zdGgEsMO0Y tm74vu8cnKIxqu8rKvJ6F0130 provenance
has publication info: NP66460.RAaOzdORfOJ2zdGgEsMO0Y tm74vu8cnKIxqu8rKvJ6F0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66460.RAaOzdORfOJ2zdGgEsMO0Y tm74vu8cnKIxqu8rKvJ6F0130 assertion
type: Assertion
description: [These findings indicate that SDC3 polymorphisms could contribute to the link between female hyperandrogenism and obesity and suggest a novel potential role for SDC3 as a modulator of gonadal steroid function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19820907
was generated by: ECO_0000203

NP66462.RAVpTZeUvv7sl1UhyCTtYmoNBAbL0CICMxSTRgyQ PF54
has assertion: NP66462.RAVpTZeUvv7sl1UhyCTtYmoNBAbL0CICMxSTRgyQ PF54130 assertion
has provenance: NP66462.RAVpTZeUvv7sl1UhyCTtYmoNBAbL0CICMxSTRgyQ PF54130 provenance
has publication info: NP66462.RAVpTZeUvv7sl1UhyCTtYmoNBAbL0CICMxSTRgyQ PF54130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66462.RAVpTZeUvv7sl1UhyCTtYmoNBAbL0CICMxSTRgyQ PF54130 assertion
type: Assertion
description: [Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset 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/17373700
was generated by: ECO_0000203

NP66466.RAT1taoe6RPDpv 7-s-XsfwyCIcKifd9cGaa-YgZrpagk
has assertion: NP66466.RAT1taoe6RPDpv 7-s-XsfwyCIcKifd9cGaa-YgZrpagk130 assertion
has provenance: NP66466.RAT1taoe6RPDpv 7-s-XsfwyCIcKifd9cGaa-YgZrpagk130 provenance
has publication info: NP66466.RAT1taoe6RPDpv 7-s-XsfwyCIcKifd9cGaa-YgZrpagk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66466.RAT1taoe6RPDpv 7-s-XsfwyCIcKifd9cGaa-YgZrpagk130 assertion
type: Assertion
description: [Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19578796
was generated by: ECO_0000203

NP66472.RASkiSKmKMRRenZ834L0yCNJjptvYaoq1uclKamAyjW24
has assertion: NP66472.RASkiSKmKMRRenZ834L0yCNJjptvYaoq1uclKamAyjW24130 assertion
has provenance: NP66472.RASkiSKmKMRRenZ834L0yCNJjptvYaoq1uclKamAyjW24130 provenance
has publication info: NP66472.RASkiSKmKMRRenZ834L0yCNJjptvYaoq1uclKamAyjW24130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66472.RASkiSKmKMRRenZ834L0yCNJjptvYaoq1uclKamAyjW24130 assertion
type: Assertion
description: [This study provides a possible association between the selectin gene polymorphisms and the rapid progression to ESRD in IgAN 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/16974056
was generated by: ECO_0000203

NP66474.RAUGDMEd9hc4tPiAoGCmd4it XmTL2CaWYGweNGAccQ6Q
has assertion: NP66474.RAUGDMEd9hc4tPiAoGCmd4it XmTL2CaWYGweNGAccQ6Q130 assertion
has provenance: NP66474.RAUGDMEd9hc4tPiAoGCmd4it XmTL2CaWYGweNGAccQ6Q130 provenance
has publication info: NP66474.RAUGDMEd9hc4tPiAoGCmd4it XmTL2CaWYGweNGAccQ6Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66474.RAUGDMEd9hc4tPiAoGCmd4it XmTL2CaWYGweNGAccQ6Q130 assertion
type: Assertion
description: [s l-selectin gene polymorphisms are associated with GD susceptibility in Chinese 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/17465998
was generated by: ECO_0000203

NP66476.RAZho- xBdQiprt D1eBU0VfAEvBAHwtM8mL6xJwSru9Y
has assertion: NP66476.RAZho- xBdQiprt D1eBU0VfAEvBAHwtM8mL6xJwSru9Y130 assertion
has provenance: NP66476.RAZho- xBdQiprt D1eBU0VfAEvBAHwtM8mL6xJwSru9Y130 provenance
has publication info: NP66476.RAZho- xBdQiprt D1eBU0VfAEvBAHwtM8mL6xJwSru9Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66476.RAZho- xBdQiprt D1eBU0VfAEvBAHwtM8mL6xJwSru9Y130 assertion
type: Assertion
description: [Increased sP-selectin concentrations are associated with VTE and genotype status. sP-selectin concentrations are lower in individuals carrying the P-selectin Pro715 variant than in those without this 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/17510305
was generated by: ECO_0000203

NP66480.RAWUAsiRugDhBCouWGEOWBwdge9Xt2NpmkIPyxdvO0zgI
has assertion: NP66480.RAWUAsiRugDhBCouWGEOWBwdge9Xt2NpmkIPyxdvO0zgI130 assertion
has provenance: NP66480.RAWUAsiRugDhBCouWGEOWBwdge9Xt2NpmkIPyxdvO0zgI130 provenance
has publication info: NP66480.RAWUAsiRugDhBCouWGEOWBwdge9Xt2NpmkIPyxdvO0zgI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66480.RAWUAsiRugDhBCouWGEOWBwdge9Xt2NpmkIPyxdvO0zgI130 assertion
type: Assertion
description: [Relationship between alpha-1 antitrypsin deficient genotypes S and Z and lung cancer in Jordanian 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/16501672
was generated by: ECO_0000203

NP66482.RAU728EAW79Bg4JOs5YSrCFr7jVI8zt6cW0wLmsw5dqiI
has assertion: NP66482.RAU728EAW79Bg4JOs5YSrCFr7jVI8zt6cW0wLmsw5dqiI130 assertion
has provenance: NP66482.RAU728EAW79Bg4JOs5YSrCFr7jVI8zt6cW0wLmsw5dqiI130 provenance
has publication info: NP66482.RAU728EAW79Bg4JOs5YSrCFr7jVI8zt6cW0wLmsw5dqiI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66482.RAU728EAW79Bg4JOs5YSrCFr7jVI8zt6cW0wLmsw5dqiI130 assertion
type: Assertion
description: [We confirm previous observations that variants of the beta adrenergic receptor and of nitric oxide synthase are associated with prematurity, and suggest that genetic variants of the placental antifibrinolytic plasminogen activator inhibitor-2, and thrombomodulin and alpha adducin may be contributors to risk of spontaneous preterm birth. LEVEL OF EVIDENCE: 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/17267840
was generated by: ECO_0000203

NP66484.RATcrfCArqcuOKEd8OQ0I-gBDaxcNuIsrKeXZQjr65iLU
has assertion: NP66484.RATcrfCArqcuOKEd8OQ0I-gBDaxcNuIsrKeXZQjr65iLU130 assertion
has provenance: NP66484.RATcrfCArqcuOKEd8OQ0I-gBDaxcNuIsrKeXZQjr65iLU130 provenance
has publication info: NP66484.RATcrfCArqcuOKEd8OQ0I-gBDaxcNuIsrKeXZQjr65iLU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP66484.RATcrfCArqcuOKEd8OQ0I-gBDaxcNuIsrKeXZQjr65iLU130 assertion
type: Assertion
description: [The polymorphism of megsin A23167G is associated with$$$ susceptibility and progression of IgA nephropathy 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/16550745
was generated by: ECO_0000203

NP66492.RAQQvJc0QtsIZIrn-QNJYttxgiOn2lbcVuIv40OTZCSvc
has assertion: NP66492.RAQQvJc0QtsIZIrn-QNJYttxgiOn2lbcVuIv40OTZCSvc130 assertion
has provenance: NP66492.RAQQvJc0QtsIZIrn-QNJYttxgiOn2lbcVuIv40OTZCSvc130 provenance
has publication info: NP66492.RAQQvJc0QtsIZIrn-QNJYttxgiOn2lbcVuIv40OTZCSvc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66492.RAQQvJc0QtsIZIrn-QNJYttxgiOn2lbcVuIv40OTZCSvc130 assertion
type: Assertion
description: [Hypofibrinolysis, associated with the 4G allele of the PAI-1 gene, was found significantly more often in women with endometriosis compared with 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/16816071
was generated by: ECO_0000203

NP66495.RAcF6OG 67AQN-tzY6PItK9AfxkzXf3NwjUiIR9oiRc3Q
has assertion: NP66495.RAcF6OG 67AQN-tzY6PItK9AfxkzXf3NwjUiIR9oiRc3Q130 assertion
has provenance: NP66495.RAcF6OG 67AQN-tzY6PItK9AfxkzXf3NwjUiIR9oiRc3Q130 provenance
has publication info: NP66495.RAcF6OG 67AQN-tzY6PItK9AfxkzXf3NwjUiIR9oiRc3Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP66495.RAcF6OG 67AQN-tzY6PItK9AfxkzXf3NwjUiIR9oiRc3Q130 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

NP66499.RAUZPwAG0uSJu3euItOJLFOKmC iv0IywUAx15y1CaX3M
has assertion: NP66499.RAUZPwAG0uSJu3euItOJLFOKmC iv0IywUAx15y1CaX3M130 assertion
has provenance: NP66499.RAUZPwAG0uSJu3euItOJLFOKmC iv0IywUAx15y1CaX3M130 provenance
has publication info: NP66499.RAUZPwAG0uSJu3euItOJLFOKmC iv0IywUAx15y1CaX3M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66499.RAUZPwAG0uSJu3euItOJLFOKmC iv0IywUAx15y1CaX3M130 assertion
type: Assertion
description: [This data provides additional evidence supporting an important role for PAI-1 in the pathogenesis of aggressive fibromatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17160433
was generated by: ECO_0000203

NP66501.RAbYuSHo3VgakP9om68p3Hp4C7wd9XeO 1NcgWEPGqTsI
has assertion: NP66501.RAbYuSHo3VgakP9om68p3Hp4C7wd9XeO 1NcgWEPGqTsI130 assertion
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has publication info: NP66501.RAbYuSHo3VgakP9om68p3Hp4C7wd9XeO 1NcgWEPGqTsI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP66501.RAbYuSHo3VgakP9om68p3Hp4C7wd9XeO 1NcgWEPGqTsI130 assertion
type: Assertion
description: [Significance of factor V, prothrombin, MTHFR, and PAI-1 genotypes in childhood cerebral thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17456624
was generated by: ECO_0000203

NP66502.RAZ8Y47v3jZn4ataoDNYbILd68ulOm8iAET3EF-CpbKAY
has assertion: NP66502.RAZ8Y47v3jZn4ataoDNYbILd68ulOm8iAET3EF-CpbKAY130 assertion
has provenance: NP66502.RAZ8Y47v3jZn4ataoDNYbILd68ulOm8iAET3EF-CpbKAY130 provenance
has publication info: NP66502.RAZ8Y47v3jZn4ataoDNYbILd68ulOm8iAET3EF-CpbKAY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP66502.RAZ8Y47v3jZn4ataoDNYbILd68ulOm8iAET3EF-CpbKAY130 assertion
type: Assertion
description: [The influence of metabolic syndrome components on plasma PAI-1 concentrations is modified by the PAI-1 4G/5G genotype and ethnicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17467713
was generated by: ECO_0000203

NP66504.RAZpvKDeYYPUoQU5tiNToQv1HXtbZBFqpbpmIciV9mbpE
has assertion: NP66504.RAZpvKDeYYPUoQU5tiNToQv1HXtbZBFqpbpmIciV9mbpE130 assertion
has provenance: NP66504.RAZpvKDeYYPUoQU5tiNToQv1HXtbZBFqpbpmIciV9mbpE130 provenance
has publication info: NP66504.RAZpvKDeYYPUoQU5tiNToQv1HXtbZBFqpbpmIciV9mbpE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66504.RAZpvKDeYYPUoQU5tiNToQv1HXtbZBFqpbpmIciV9mbpE130 assertion
type: Assertion
description: [PAI-1 gene expression decreased over time after CPB. We found a link between PAI-1 genotype, PAI gene expression, and transfusion of coagulation products after cardiac 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/17513622
was generated by: ECO_0000203

NP66506.RAR77xpd880oWs6pxVM2D1qS7iK7SrZ33g14bC0xoo Ww
has assertion: NP66506.RAR77xpd880oWs6pxVM2D1qS7iK7SrZ33g14bC0xoo Ww130 assertion
has provenance: NP66506.RAR77xpd880oWs6pxVM2D1qS7iK7SrZ33g14bC0xoo Ww130 provenance
has publication info: NP66506.RAR77xpd880oWs6pxVM2D1qS7iK7SrZ33g14bC0xoo Ww130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP66506.RAR77xpd880oWs6pxVM2D1qS7iK7SrZ33g14bC0xoo Ww130 assertion
type: Assertion
description: [A functional SNP in the promoter of the SERPINH1 gene increases risk of preterm premature rupture of membranes 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/16938879
was generated by: ECO_0000203

NP66507.RAXO7TVKpmCb gUr0XjKtmknIShAGZLc4jkLoB7YEgwws
has assertion: NP66507.RAXO7TVKpmCb gUr0XjKtmknIShAGZLc4jkLoB7YEgwws130 assertion
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has publication info: NP66507.RAXO7TVKpmCb gUr0XjKtmknIShAGZLc4jkLoB7YEgwws130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66507.RAXO7TVKpmCb gUr0XjKtmknIShAGZLc4jkLoB7YEgwws130 assertion
type: Assertion
description: [A 12-bp deletion in the 5'-flanking region of the SERPINH1 gene affects promoter activity and protects against preterm premature rupture of membranes 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/18205191
was generated by: ECO_0000203

NP66516.RAW m7ajcLqkcbeKb7FoqZ oV56moqRjuY2JLxex5h GM
has assertion: NP66516.RAW m7ajcLqkcbeKb7FoqZ oV56moqRjuY2JLxex5h GM130 assertion
has provenance: NP66516.RAW m7ajcLqkcbeKb7FoqZ oV56moqRjuY2JLxex5h GM130 provenance
has publication info: NP66516.RAW m7ajcLqkcbeKb7FoqZ oV56moqRjuY2JLxex5h GM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66516.RAW m7ajcLqkcbeKb7FoqZ oV56moqRjuY2JLxex5h GM130 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

NP66517.RAbII-pnPINHbUAl5K4iCaZmQwRXJ6ekZl4QawqbuedR4
has assertion: NP66517.RAbII-pnPINHbUAl5K4iCaZmQwRXJ6ekZl4QawqbuedR4130 assertion
has provenance: NP66517.RAbII-pnPINHbUAl5K4iCaZmQwRXJ6ekZl4QawqbuedR4130 provenance
has publication info: NP66517.RAbII-pnPINHbUAl5K4iCaZmQwRXJ6ekZl4QawqbuedR4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP66517.RAbII-pnPINHbUAl5K4iCaZmQwRXJ6ekZl4QawqbuedR4130 assertion
type: Assertion
description: [Association of endometrial cancer risk with a functional polymorphism (Asp(327)Asn) in the sex hormone-binding globulin 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/17315164
was generated by: ECO_0000203

NP66519.RAYlWcLsMMVg3dhL87WiZ4dpuQ0AOZYxU9uXclefRewak
has assertion: NP66519.RAYlWcLsMMVg3dhL87WiZ4dpuQ0AOZYxU9uXclefRewak130 assertion
has provenance: NP66519.RAYlWcLsMMVg3dhL87WiZ4dpuQ0AOZYxU9uXclefRewak130 provenance
has publication info: NP66519.RAYlWcLsMMVg3dhL87WiZ4dpuQ0AOZYxU9uXclefRewak130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66519.RAYlWcLsMMVg3dhL87WiZ4dpuQ0AOZYxU9uXclefRewak130 assertion
type: Assertion
description: [Similarly, homozygosity for the C1420T SHMT polymorphism also had a 2.6-fold increased risk (95% CI: 1.1, 5.9) of developing 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/18996879
was generated by: ECO_0000203

NP66529.RAV9P6HYV IubzGYuM9kZvjlqC3oeyqW6MjQN1LOXjKi0
has assertion: NP66529.RAV9P6HYV IubzGYuM9kZvjlqC3oeyqW6MjQN1LOXjKi0130 assertion
has provenance: NP66529.RAV9P6HYV IubzGYuM9kZvjlqC3oeyqW6MjQN1LOXjKi0130 provenance
has publication info: NP66529.RAV9P6HYV IubzGYuM9kZvjlqC3oeyqW6MjQN1LOXjKi0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66529.RAV9P6HYV IubzGYuM9kZvjlqC3oeyqW6MjQN1LOXjKi0130 assertion
type: Assertion
description: [Mutation analysis of the seven in absentia homolog 1 (SIAH1) gene in 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/16752048
was generated by: ECO_0000203

NP66538.RASwOz7v1vCgw4wlqwvyaU2 CXah9uyZ24031E8wReCMA
has assertion: NP66538.RASwOz7v1vCgw4wlqwvyaU2 CXah9uyZ24031E8wReCMA130 assertion
has provenance: NP66538.RASwOz7v1vCgw4wlqwvyaU2 CXah9uyZ24031E8wReCMA130 provenance
has publication info: NP66538.RASwOz7v1vCgw4wlqwvyaU2 CXah9uyZ24031E8wReCMA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66538.RASwOz7v1vCgw4wlqwvyaU2 CXah9uyZ24031E8wReCMA130 assertion
type: Assertion
description: [SLC12A3 (solute carrier family 12 member sodium/chloride 3) polymorphisms are associated with end-stage renal disease in 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/16505253
was generated by: ECO_0000203

NP66540.RAf0Rr1TqeIHOTYr-r4PIdszHPTUs5SrK8AK4YiiXvdqM
has assertion: NP66540.RAf0Rr1TqeIHOTYr-r4PIdszHPTUs5SrK8AK4YiiXvdqM130 assertion
has provenance: NP66540.RAf0Rr1TqeIHOTYr-r4PIdszHPTUs5SrK8AK4YiiXvdqM130 provenance
has publication info: NP66540.RAf0Rr1TqeIHOTYr-r4PIdszHPTUs5SrK8AK4YiiXvdqM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66540.RAf0Rr1TqeIHOTYr-r4PIdszHPTUs5SrK8AK4YiiXvdqM130 assertion
type: Assertion
description: [Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16917939
was generated by: ECO_0000203

NP66550.RAWIBw4fCalx1Py3JJUxv6-ZFVAagLW3ZJnCAnZE-e8EE
has assertion: NP66550.RAWIBw4fCalx1Py3JJUxv6-ZFVAagLW3ZJnCAnZE-e8EE130 assertion
has provenance: NP66550.RAWIBw4fCalx1Py3JJUxv6-ZFVAagLW3ZJnCAnZE-e8EE130 provenance
has publication info: NP66550.RAWIBw4fCalx1Py3JJUxv6-ZFVAagLW3ZJnCAnZE-e8EE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66550.RAWIBw4fCalx1Py3JJUxv6-ZFVAagLW3ZJnCAnZE-e8EE130 assertion
type: Assertion
description: [Analysis of chromosome 5q31-32 and psoriasis: confirmation of a susceptibility locus but no association with SNPs within SLC22A4 and SLC22A5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16484987
was generated by: ECO_0000203

NP66551.RAen8QxhO91zCSBvDIE8KunLftLyE4-FAboKwebpFBZOg
has assertion: NP66551.RAen8QxhO91zCSBvDIE8KunLftLyE4-FAboKwebpFBZOg130 assertion
has provenance: NP66551.RAen8QxhO91zCSBvDIE8KunLftLyE4-FAboKwebpFBZOg130 provenance
has publication info: NP66551.RAen8QxhO91zCSBvDIE8KunLftLyE4-FAboKwebpFBZOg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66551.RAen8QxhO91zCSBvDIE8KunLftLyE4-FAboKwebpFBZOg130 assertion
type: Assertion
description: [Analysis of chromosome 5q31-32 and psoriasis: confirmation of a susceptibility locus but no association with SNPs within SLC22A4 and SLC22A5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16484987
was generated by: ECO_0000203

NP66562.RAZDbCQxaQkxonMRF2l80v5hwce8MJBIshHjqka1KVB34
has assertion: NP66562.RAZDbCQxaQkxonMRF2l80v5hwce8MJBIshHjqka1KVB34130 assertion
has provenance: NP66562.RAZDbCQxaQkxonMRF2l80v5hwce8MJBIshHjqka1KVB34130 provenance
has publication info: NP66562.RAZDbCQxaQkxonMRF2l80v5hwce8MJBIshHjqka1KVB34130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66562.RAZDbCQxaQkxonMRF2l80v5hwce8MJBIshHjqka1KVB34130 assertion
type: Assertion
description: [DAT VNTR 10/10 genotype may be associated with an endophenotype of late-life depression with executive dysfunction that responds preferentially to methylphenidate added to a selective serotonin reuptake inhibitor, which warrants replication in a large sample. Copyright (c) 2007 John Wiley & Sons, Ltd.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17621383
was generated by: ECO_0000203

NP66564.RAeolb3cdSt4TtH-LQnXiDtMqTrxSxwDCBc6yE1jJnx2Y
has assertion: NP66564.RAeolb3cdSt4TtH-LQnXiDtMqTrxSxwDCBc6yE1jJnx2Y130 assertion
has provenance: NP66564.RAeolb3cdSt4TtH-LQnXiDtMqTrxSxwDCBc6yE1jJnx2Y130 provenance
has publication info: NP66564.RAeolb3cdSt4TtH-LQnXiDtMqTrxSxwDCBc6yE1jJnx2Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66564.RAeolb3cdSt4TtH-LQnXiDtMqTrxSxwDCBc6yE1jJnx2Y130 assertion
type: Assertion
description: [Serotonin and dopamine transporter genes do not influence depression in 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/18973248
was generated by: ECO_0000203

NP66568.RAdFleHZjz1XYegf1lXpc2HCiIVkoufGfNNYAninr3I90
has assertion: NP66568.RAdFleHZjz1XYegf1lXpc2HCiIVkoufGfNNYAninr3I90130 assertion
has provenance: NP66568.RAdFleHZjz1XYegf1lXpc2HCiIVkoufGfNNYAninr3I90130 provenance
has publication info: NP66568.RAdFleHZjz1XYegf1lXpc2HCiIVkoufGfNNYAninr3I90130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66568.RAdFleHZjz1XYegf1lXpc2HCiIVkoufGfNNYAninr3I90130 assertion
type: Assertion
description: [Association of C/T polymorphism in intron 14 of the dopamine transporter gene (rs40184) with major depression in a northeastern Thai 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/20391341
was generated by: ECO_0000203

NP66575.RAZ90UdIiVDh8NoqiLsRAG8DHSfK19UHGmGuz e3tdOWM
has assertion: NP66575.RAZ90UdIiVDh8NoqiLsRAG8DHSfK19UHGmGuz e3tdOWM130 assertion
has provenance: NP66575.RAZ90UdIiVDh8NoqiLsRAG8DHSfK19UHGmGuz e3tdOWM130 provenance
has publication info: NP66575.RAZ90UdIiVDh8NoqiLsRAG8DHSfK19UHGmGuz e3tdOWM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66575.RAZ90UdIiVDh8NoqiLsRAG8DHSfK19UHGmGuz e3tdOWM130 assertion
type: Assertion
description: [the S allele of the SLC6A4 promoter variant is associated with overweight being an independent genetic risk factor for 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/17299098
was generated by: ECO_0000203

NP66580.RAX z2bE B1poWe-au4blgKXsThhFT80GGOTytpot03JE
has assertion: NP66580.RAX z2bE B1poWe-au4blgKXsThhFT80GGOTytpot03JE130 assertion
has provenance: NP66580.RAX z2bE B1poWe-au4blgKXsThhFT80GGOTytpot03JE130 provenance
has publication info: NP66580.RAX z2bE B1poWe-au4blgKXsThhFT80GGOTytpot03JE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66580.RAX z2bE B1poWe-au4blgKXsThhFT80GGOTytpot03JE130 assertion
type: Assertion
description: [X-linked creatine transporter (SLC6A8) mutations in about 1% of males with mental retardation of unknown etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16738945
was generated by: ECO_0000203

NP66581.RAexRX8UBF EDOrwrzYRTzBb04MKn24P5HDq1hZ HZFQk
has assertion: NP66581.RAexRX8UBF EDOrwrzYRTzBb04MKn24P5HDq1hZ HZFQk130 assertion
has provenance: NP66581.RAexRX8UBF EDOrwrzYRTzBb04MKn24P5HDq1hZ HZFQk130 provenance
has publication info: NP66581.RAexRX8UBF EDOrwrzYRTzBb04MKn24P5HDq1hZ HZFQk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66581.RAexRX8UBF EDOrwrzYRTzBb04MKn24P5HDq1hZ HZFQk130 assertion
type: Assertion
description: [Association study of polymorphisms in glycine transporter 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/16604304
was generated by: ECO_0000203

NP66583.RAehD5HM7wMBDebVu6nzhb-gxetw-fY-rAUoj51Mdo Zo
has assertion: NP66583.RAehD5HM7wMBDebVu6nzhb-gxetw-fY-rAUoj51Mdo Zo130 assertion
has provenance: NP66583.RAehD5HM7wMBDebVu6nzhb-gxetw-fY-rAUoj51Mdo Zo130 provenance
has publication info: NP66583.RAehD5HM7wMBDebVu6nzhb-gxetw-fY-rAUoj51Mdo Zo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66583.RAehD5HM7wMBDebVu6nzhb-gxetw-fY-rAUoj51Mdo Zo130 assertion
type: Assertion
description: [We concluded that at least one susceptibility locus for schizophrenia may be located within or nearby SLC6A5, whereas SLC1A4, SLC1A5 and SLC6A9 are unlikely to be major susceptibility genes for schizophrenia 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/18638388
was generated by: ECO_0000203

NP66587.RAQfveHfWRH4dbE6-PEYk fjwRjwXQnP06wzr5DY2CC3Y
has assertion: NP66587.RAQfveHfWRH4dbE6-PEYk fjwRjwXQnP06wzr5DY2CC3Y130 assertion
has provenance: NP66587.RAQfveHfWRH4dbE6-PEYk fjwRjwXQnP06wzr5DY2CC3Y130 provenance
has publication info: NP66587.RAQfveHfWRH4dbE6-PEYk fjwRjwXQnP06wzr5DY2CC3Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66587.RAQfveHfWRH4dbE6-PEYk fjwRjwXQnP06wzr5DY2CC3Y130 assertion
type: Assertion
description: [Neither of the SNCB SNPs examined were associated with PD overall or in strata, and haplotype analyses were negative 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/17556099
was generated by: ECO_0000203

NP66594.RASUACfzGDAl1pMbME4LkyyUpS2UKiVzf6fQs8mSGUXwo
has assertion: NP66594.RASUACfzGDAl1pMbME4LkyyUpS2UKiVzf6fQs8mSGUXwo130 assertion
has provenance: NP66594.RASUACfzGDAl1pMbME4LkyyUpS2UKiVzf6fQs8mSGUXwo130 provenance
has publication info: NP66594.RASUACfzGDAl1pMbME4LkyyUpS2UKiVzf6fQs8mSGUXwo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66594.RASUACfzGDAl1pMbME4LkyyUpS2UKiVzf6fQs8mSGUXwo130 assertion
type: Assertion
description: [Polymorphisms of the gene coding for copper/zinc superoxide dismutase (SOD1) in patients with Japanese encephalitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16989689
was generated by: ECO_0000203

NP66598.RAZBJdbKdUADGTJpykVHy0bfhoTGHxfXtUNsnoabaMKAw
has assertion: NP66598.RAZBJdbKdUADGTJpykVHy0bfhoTGHxfXtUNsnoabaMKAw130 assertion
has provenance: NP66598.RAZBJdbKdUADGTJpykVHy0bfhoTGHxfXtUNsnoabaMKAw130 provenance
has publication info: NP66598.RAZBJdbKdUADGTJpykVHy0bfhoTGHxfXtUNsnoabaMKAw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66598.RAZBJdbKdUADGTJpykVHy0bfhoTGHxfXtUNsnoabaMKAw130 assertion
type: Assertion
description: [Genetic polymorphisms in nitric oxide synthase genes modify the relationship between vegetable and fruit intake and risk of 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/19423521
was generated by: ECO_0000203

NP66599.RAZtaOvr-X819zwOjRHXirzsfAP4dNeBguAJOgS9bZDPQ
has assertion: NP66599.RAZtaOvr-X819zwOjRHXirzsfAP4dNeBguAJOgS9bZDPQ130 assertion
has provenance: NP66599.RAZtaOvr-X819zwOjRHXirzsfAP4dNeBguAJOgS9bZDPQ130 provenance
has publication info: NP66599.RAZtaOvr-X819zwOjRHXirzsfAP4dNeBguAJOgS9bZDPQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66599.RAZtaOvr-X819zwOjRHXirzsfAP4dNeBguAJOgS9bZDPQ130 assertion
type: Assertion
description: [Manganese superoxide dismutase polymorphism in chronic pelvic pain 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/16847469
was generated by: ECO_0000203

NP66609.RAcTJ2qfgD1IbCHfEaMb6NTS7KQzMiSf0GasBhCzWZcww
has assertion: NP66609.RAcTJ2qfgD1IbCHfEaMb6NTS7KQzMiSf0GasBhCzWZcww130 assertion
has provenance: NP66609.RAcTJ2qfgD1IbCHfEaMb6NTS7KQzMiSf0GasBhCzWZcww130 provenance
has publication info: NP66609.RAcTJ2qfgD1IbCHfEaMb6NTS7KQzMiSf0GasBhCzWZcww130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66609.RAcTJ2qfgD1IbCHfEaMb6NTS7KQzMiSf0GasBhCzWZcww130 assertion
type: Assertion
description: [The MnSOD mutant C allele may increase the susceptibility to DILI, and GSTM1 null genotype may be related to anti-tuberculosis drug-induced hepatotoxicity. Determination of the MnSOD and GSTM1 genotypes may help identify patients at high risk for DILI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17400324
was generated by: ECO_0000203

NP66615.RAbmPhnskqLolf8BeFwgROrTxsszuh4j8fR2-EvBdPxFI
has assertion: NP66615.RAbmPhnskqLolf8BeFwgROrTxsszuh4j8fR2-EvBdPxFI130 assertion
has provenance: NP66615.RAbmPhnskqLolf8BeFwgROrTxsszuh4j8fR2-EvBdPxFI130 provenance
has publication info: NP66615.RAbmPhnskqLolf8BeFwgROrTxsszuh4j8fR2-EvBdPxFI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66615.RAbmPhnskqLolf8BeFwgROrTxsszuh4j8fR2-EvBdPxFI130 assertion
type: Assertion
description: [In this study, we tested 27 genes (ACE, BDNF, CH25H, CHRNB2, CST3, CTSD, DAPK1, GALP, hCG2039140, IL1B, LMNA, LOC439999, LOC651924, MAPT, MTHFR, MYH13, PCK1, PGBD1, PRNP, PSEN1, SORCS1, SORL1, TF, TFAM, TNK1, GWA_14q32.13, and GWA_7p15.2), all showing significant association with AD risk in the AlzGene meta-analyses, in a large collection of family-based samples comprised of 4,180 subjects from over 1,300 pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18830724
was generated by: ECO_0000203

NP66617.RAfmSZZj-4BV5G-7KerWAUjnfrysSlY0-b6mOKjQ7NCLc
has assertion: NP66617.RAfmSZZj-4BV5G-7KerWAUjnfrysSlY0-b6mOKjQ7NCLc130 assertion
has provenance: NP66617.RAfmSZZj-4BV5G-7KerWAUjnfrysSlY0-b6mOKjQ7NCLc130 provenance
has publication info: NP66617.RAfmSZZj-4BV5G-7KerWAUjnfrysSlY0-b6mOKjQ7NCLc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66617.RAfmSZZj-4BV5G-7KerWAUjnfrysSlY0-b6mOKjQ7NCLc130 assertion
type: Assertion
description: [SORL1 has recently been identified as a major genetic contributor to increased risk for late-onset Alzheimer 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/18407551
was generated by: ECO_0000203

NP66621.RAZvj0SdbeUOAEeydQK5VSPitrgtvVFKU YKkQC9BOU-8
has assertion: NP66621.RAZvj0SdbeUOAEeydQK5VSPitrgtvVFKU YKkQC9BOU-8130 assertion
has provenance: NP66621.RAZvj0SdbeUOAEeydQK5VSPitrgtvVFKU YKkQC9BOU-8130 provenance
has publication info: NP66621.RAZvj0SdbeUOAEeydQK5VSPitrgtvVFKU YKkQC9BOU-8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66621.RAZvj0SdbeUOAEeydQK5VSPitrgtvVFKU YKkQC9BOU-8130 assertion
type: Assertion
description: [Candidate gene association study of insulin signaling genes and Alzheimer's disease: evidence for SOS2, PCK1, and PPARgamma as susceptibility 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/17440948
was generated by: ECO_0000203

NP66626.RAbdPNZE1y2-n21-90jMDq 3kqG KtTcKd9vggNhjgLBE
has assertion: NP66626.RAbdPNZE1y2-n21-90jMDq 3kqG KtTcKd9vggNhjgLBE130 assertion
has provenance: NP66626.RAbdPNZE1y2-n21-90jMDq 3kqG KtTcKd9vggNhjgLBE130 provenance
has publication info: NP66626.RAbdPNZE1y2-n21-90jMDq 3kqG KtTcKd9vggNhjgLBE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66626.RAbdPNZE1y2-n21-90jMDq 3kqG KtTcKd9vggNhjgLBE130 assertion
type: Assertion
description: [Our aim was to assess the gut mucosal gene expression and genetic association of SPINK1, -2, -4, and -5 in the Dutch CD 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/17333166
was generated by: ECO_0000203

NP66627.RAZcIXSIApBoh5wc59FkADy1FMUECQD8LvcO5-L1hib30
has assertion: NP66627.RAZcIXSIApBoh5wc59FkADy1FMUECQD8LvcO5-L1hib30130 assertion
has provenance: NP66627.RAZcIXSIApBoh5wc59FkADy1FMUECQD8LvcO5-L1hib30130 provenance
has publication info: NP66627.RAZcIXSIApBoh5wc59FkADy1FMUECQD8LvcO5-L1hib30130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66627.RAZcIXSIApBoh5wc59FkADy1FMUECQD8LvcO5-L1hib30130 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

NP66632.RAeUcY59wAhkZLFeendp7qVOigpQA-rb6ukBPf 7mfDJg
has assertion: NP66632.RAeUcY59wAhkZLFeendp7qVOigpQA-rb6ukBPf 7mfDJg130 assertion
has provenance: NP66632.RAeUcY59wAhkZLFeendp7qVOigpQA-rb6ukBPf 7mfDJg130 provenance
has publication info: NP66632.RAeUcY59wAhkZLFeendp7qVOigpQA-rb6ukBPf 7mfDJg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66632.RAeUcY59wAhkZLFeendp7qVOigpQA-rb6ukBPf 7mfDJg130 assertion
type: Assertion
description: [These results are the first to demonstrate the existence of T-593A promoter polymorphism of the OPN gene and significant association with risk of developing nephrolithiasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21044748
was generated by: ECO_0000203

NP66634.RAfwPAvWm3MACEQsG2EJi0sicnxvHl-lxcm 8w992eXs0
has assertion: NP66634.RAfwPAvWm3MACEQsG2EJi0sicnxvHl-lxcm 8w992eXs0130 assertion
has provenance: NP66634.RAfwPAvWm3MACEQsG2EJi0sicnxvHl-lxcm 8w992eXs0130 provenance
has publication info: NP66634.RAfwPAvWm3MACEQsG2EJi0sicnxvHl-lxcm 8w992eXs0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66634.RAfwPAvWm3MACEQsG2EJi0sicnxvHl-lxcm 8w992eXs0130 assertion
type: Assertion
description: [ In summary, we replicated our previous finding and found evidence for SNPs in the 5 region of the SREBF1c gene to be associated with the risk of type 2 diabetes and plasma glucose concentration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17019602
was generated by: ECO_0000203

NP66635.RAUCryxCq hDuJuSbMD8DpUOUBJZUkFOK-sK9UJ-3WajU
has assertion: NP66635.RAUCryxCq hDuJuSbMD8DpUOUBJZUkFOK-sK9UJ-3WajU130 assertion
has provenance: NP66635.RAUCryxCq hDuJuSbMD8DpUOUBJZUkFOK-sK9UJ-3WajU130 provenance
has publication info: NP66635.RAUCryxCq hDuJuSbMD8DpUOUBJZUkFOK-sK9UJ-3WajU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66635.RAUCryxCq hDuJuSbMD8DpUOUBJZUkFOK-sK9UJ-3WajU130 assertion
type: Assertion
description: [Association of sterol regulatory element-binding protein-1c gene polymorphism with type 2 diabetes mellitus, insulin resistance and blood lipid levels 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/18692268
was generated by: ECO_0000203

NP66637.RAW2KsRJkpMI dGEWjh0W0DTvmd8tTTOQsAT9Kwpc eI8
has assertion: NP66637.RAW2KsRJkpMI dGEWjh0W0DTvmd8tTTOQsAT9Kwpc eI8130 assertion
has provenance: NP66637.RAW2KsRJkpMI dGEWjh0W0DTvmd8tTTOQsAT9Kwpc eI8130 provenance
has publication info: NP66637.RAW2KsRJkpMI dGEWjh0W0DTvmd8tTTOQsAT9Kwpc eI8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66637.RAW2KsRJkpMI dGEWjh0W0DTvmd8tTTOQsAT9Kwpc eI8130 assertion
type: Assertion
description: [We evaluated the association of variants in the sterol regulatory element-binding factor 1 gene (SREBF1) with 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/18192539
was generated by: ECO_0000203

NP66648.RAeuqiypvfGrChkl5JEGNRNVsOmaum9E8pSKaM38Ostgo
has assertion: NP66648.RAeuqiypvfGrChkl5JEGNRNVsOmaum9E8pSKaM38Ostgo130 assertion
has provenance: NP66648.RAeuqiypvfGrChkl5JEGNRNVsOmaum9E8pSKaM38Ostgo130 provenance
has publication info: NP66648.RAeuqiypvfGrChkl5JEGNRNVsOmaum9E8pSKaM38Ostgo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66648.RAeuqiypvfGrChkl5JEGNRNVsOmaum9E8pSKaM38Ostgo130 assertion
type: Assertion
description: [, LKB1 gene mutations were relatively rare in Japanese patients with lung cancer compared with Caucasian 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/17711506
was generated by: ECO_0000203

NP66654.RAedopyWHAYy-CQSa2BWv3cXLp4InpEJA9zTrm 4EuPTk
has assertion: NP66654.RAedopyWHAYy-CQSa2BWv3cXLp4InpEJA9zTrm 4EuPTk130 assertion
has provenance: NP66654.RAedopyWHAYy-CQSa2BWv3cXLp4InpEJA9zTrm 4EuPTk130 provenance
has publication info: NP66654.RAedopyWHAYy-CQSa2BWv3cXLp4InpEJA9zTrm 4EuPTk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66654.RAedopyWHAYy-CQSa2BWv3cXLp4InpEJA9zTrm 4EuPTk130 assertion
type: Assertion
description: [This study presents genetic evidence suggesting a potential role of SULT2A1, but not STS, in the inherited AA excess of 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/17426092
was generated by: ECO_0000203

NP66656.RAXsRrqBPYES1-UUJjK8R1z7oMGASeveTjuQ9xUvJd2Nk
has assertion: NP66656.RAXsRrqBPYES1-UUJjK8R1z7oMGASeveTjuQ9xUvJd2Nk130 assertion
has provenance: NP66656.RAXsRrqBPYES1-UUJjK8R1z7oMGASeveTjuQ9xUvJd2Nk130 provenance
has publication info: NP66656.RAXsRrqBPYES1-UUJjK8R1z7oMGASeveTjuQ9xUvJd2Nk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66656.RAXsRrqBPYES1-UUJjK8R1z7oMGASeveTjuQ9xUvJd2Nk130 assertion
type: Assertion
description: [Novel polymorphisms in the SUV39H2 histone methyltransferase 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/16774942
was generated by: ECO_0000203

NP66660.RAfSXFMvuNZLO4LWxL86IzMLf EjscPJlNPuQDaYZYJh4
has assertion: NP66660.RAfSXFMvuNZLO4LWxL86IzMLf EjscPJlNPuQDaYZYJh4130 assertion
has provenance: NP66660.RAfSXFMvuNZLO4LWxL86IzMLf EjscPJlNPuQDaYZYJh4130 provenance
has publication info: NP66660.RAfSXFMvuNZLO4LWxL86IzMLf EjscPJlNPuQDaYZYJh4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66660.RAfSXFMvuNZLO4LWxL86IzMLf EjscPJlNPuQDaYZYJh4130 assertion
type: Assertion
description: [Epistasis between a set of variations located in the TAAR6 and HSP-70 genes toward schizophrenia and response to antipsychotic 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/19643584
was generated by: ECO_0000203

NP66663.RAVN-kqASNMtkv162wQRivNNaL-qhVP7-w1SyPBrFB3Rc
has assertion: NP66663.RAVN-kqASNMtkv162wQRivNNaL-qhVP7-w1SyPBrFB3Rc130 assertion
has provenance: NP66663.RAVN-kqASNMtkv162wQRivNNaL-qhVP7-w1SyPBrFB3Rc130 provenance
has publication info: NP66663.RAVN-kqASNMtkv162wQRivNNaL-qhVP7-w1SyPBrFB3Rc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66663.RAVN-kqASNMtkv162wQRivNNaL-qhVP7-w1SyPBrFB3Rc130 assertion
type: Assertion
description: [The effect of genetic variants in the thrombin activatable fibrinolysis inhibitor (TAFI) gene on TAFI-antigen levels, clot lysis time and the risk of venous thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16803573
was generated by: ECO_0000203

NP66665.RAZY5oledYkfq6raqUUy B15mnkYIQF8fWcqMyZWr29eg
has assertion: NP66665.RAZY5oledYkfq6raqUUy B15mnkYIQF8fWcqMyZWr29eg130 assertion
has provenance: NP66665.RAZY5oledYkfq6raqUUy B15mnkYIQF8fWcqMyZWr29eg130 provenance
has publication info: NP66665.RAZY5oledYkfq6raqUUy B15mnkYIQF8fWcqMyZWr29eg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66665.RAZY5oledYkfq6raqUUy B15mnkYIQF8fWcqMyZWr29eg130 assertion
type: Assertion
description: [The role of TAP1 and TAP2 gene polymorphism in idiopathic bronchiectasis 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/17245734
was generated by: ECO_0000203

NP66666.RAefKLRqhKIjyV5iUA0qQtjSySaddbnb0LYRUD0zc4t5c
has assertion: NP66666.RAefKLRqhKIjyV5iUA0qQtjSySaddbnb0LYRUD0zc4t5c130 assertion
has provenance: NP66666.RAefKLRqhKIjyV5iUA0qQtjSySaddbnb0LYRUD0zc4t5c130 provenance
has publication info: NP66666.RAefKLRqhKIjyV5iUA0qQtjSySaddbnb0LYRUD0zc4t5c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66666.RAefKLRqhKIjyV5iUA0qQtjSySaddbnb0LYRUD0zc4t5c130 assertion
type: Assertion
description: [TAP1 gene polymorphisms and nasopharyngeal carcinoma risk in a 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/17498556
was generated by: ECO_0000203

NP66667.RAe-kcUUPIu3PpjjVWiG3PA-OznfXcjy1mzJ3rUpDL3lc
has assertion: NP66667.RAe-kcUUPIu3PpjjVWiG3PA-OznfXcjy1mzJ3rUpDL3lc130 assertion
has provenance: NP66667.RAe-kcUUPIu3PpjjVWiG3PA-OznfXcjy1mzJ3rUpDL3lc130 provenance
has publication info: NP66667.RAe-kcUUPIu3PpjjVWiG3PA-OznfXcjy1mzJ3rUpDL3lc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66667.RAe-kcUUPIu3PpjjVWiG3PA-OznfXcjy1mzJ3rUpDL3lc130 assertion
type: Assertion
description: [Of the seven polymorphisms, three of which (LMP7 codons 145, TAP1 codons 637, and TAP2 codons 651) were observed to have statistically significant association with HBV infection (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/17525827
was generated by: ECO_0000203

NP66674.RAcJP1aPZkr3tL2gyNI1REPb d2w9WWrO1mOQsFB6d9yA
has assertion: NP66674.RAcJP1aPZkr3tL2gyNI1REPb d2w9WWrO1mOQsFB6d9yA130 assertion
has provenance: NP66674.RAcJP1aPZkr3tL2gyNI1REPb d2w9WWrO1mOQsFB6d9yA130 provenance
has publication info: NP66674.RAcJP1aPZkr3tL2gyNI1REPb d2w9WWrO1mOQsFB6d9yA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66674.RAcJP1aPZkr3tL2gyNI1REPb d2w9WWrO1mOQsFB6d9yA130 assertion
type: Assertion
description: [We selected 208 hepatitis B patients and 213 healthy volunteers to examine whether polymorphisms or haplotypes of the TBX21 gene promoter were associated with hepatitis B virus (HBV) infection in the 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/17378728
was generated by: ECO_0000203

NP66675.RAeFUuR0r3YFRD83byn it9WXc01205ibLz4WUREcrLzk
has assertion: NP66675.RAeFUuR0r3YFRD83byn it9WXc01205ibLz4WUREcrLzk130 assertion
has provenance: NP66675.RAeFUuR0r3YFRD83byn it9WXc01205ibLz4WUREcrLzk130 provenance
has publication info: NP66675.RAeFUuR0r3YFRD83byn it9WXc01205ibLz4WUREcrLzk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66675.RAeFUuR0r3YFRD83byn it9WXc01205ibLz4WUREcrLzk130 assertion
type: Assertion
description: [Association of TBX21 T-1993C polymorphism with viral persistence but not disease progression in hepatitis B virus 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/19473434
was generated by: ECO_0000203

NP66678.RASWMLudFQh7hEH2x1ESNIEbbK49aYFV2oMHTEbTzpwZ0
has assertion: NP66678.RASWMLudFQh7hEH2x1ESNIEbbK49aYFV2oMHTEbTzpwZ0130 assertion
has provenance: NP66678.RASWMLudFQh7hEH2x1ESNIEbbK49aYFV2oMHTEbTzpwZ0130 provenance
has publication info: NP66678.RASWMLudFQh7hEH2x1ESNIEbbK49aYFV2oMHTEbTzpwZ0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66678.RASWMLudFQh7hEH2x1ESNIEbbK49aYFV2oMHTEbTzpwZ0130 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

NP66689.RAfnIm5 Tn14xVZUuzgW2kYuBmWqvHvNlJaRKbv0EXpbo
has assertion: NP66689.RAfnIm5 Tn14xVZUuzgW2kYuBmWqvHvNlJaRKbv0EXpbo130 assertion
has provenance: NP66689.RAfnIm5 Tn14xVZUuzgW2kYuBmWqvHvNlJaRKbv0EXpbo130 provenance
has publication info: NP66689.RAfnIm5 Tn14xVZUuzgW2kYuBmWqvHvNlJaRKbv0EXpbo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66689.RAfnIm5 Tn14xVZUuzgW2kYuBmWqvHvNlJaRKbv0EXpbo130 assertion
type: Assertion
description: [Influence of MMP-2 and MMP-9 promoter polymorphisms on gene expression and clinical outcome 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/17208328
was generated by: ECO_0000203

NP66692.RAV JhKygJPrWiXNPchHSdQRok Prhr-nbVBGDQbChZ8
has assertion: NP66692.RAV JhKygJPrWiXNPchHSdQRok Prhr-nbVBGDQbChZ8130 assertion
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has publication info: NP66692.RAV JhKygJPrWiXNPchHSdQRok Prhr-nbVBGDQbChZ8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66692.RAV JhKygJPrWiXNPchHSdQRok Prhr-nbVBGDQbChZ8130 assertion
type: Assertion
description: [Individuals carrying at least one arginine at position 74 of the DRbeta1 chain (denoted the R- genotype) have a significantly increased risk of GD, as do individuals homozygous for the single nucleotide protein (SNP) in exon 33 of the Tg gene (denoted the CC 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/16646680
was generated by: ECO_0000203

NP66694.RAWD EMYg0TII00UmmE8GZf-1yOGo1CK10PAKE5VdwEcA
has assertion: NP66694.RAWD EMYg0TII00UmmE8GZf-1yOGo1CK10PAKE5VdwEcA130 assertion
has provenance: NP66694.RAWD EMYg0TII00UmmE8GZf-1yOGo1CK10PAKE5VdwEcA130 provenance
has publication info: NP66694.RAWD EMYg0TII00UmmE8GZf-1yOGo1CK10PAKE5VdwEcA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66694.RAWD EMYg0TII00UmmE8GZf-1yOGo1CK10PAKE5VdwEcA130 assertion
type: Assertion
description: [The thyroglobulin (Tg) is a major autoantigen for GD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17550957
was generated by: ECO_0000203

NP66697.RAYvqFIJ8OUl0EByIoNU1SGYpGBshjuQscd1rT5tcHud4
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has publication info: NP66697.RAYvqFIJ8OUl0EByIoNU1SGYpGBshjuQscd1rT5tcHud4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66697.RAYvqFIJ8OUl0EByIoNU1SGYpGBshjuQscd1rT5tcHud4130 assertion
type: Assertion
description: [Association of CD40 and thyroglobulin genes with later-onset Graves' disease in Taiwanese 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/18755875
was generated by: ECO_0000203

NP66699.RAaXFLAxjjbjT-9iK74pWteemknFkDGqGLvSOfEm HUzM
has assertion: NP66699.RAaXFLAxjjbjT-9iK74pWteemknFkDGqGLvSOfEm HUzM130 assertion
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has publication info: NP66699.RAaXFLAxjjbjT-9iK74pWteemknFkDGqGLvSOfEm HUzM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66699.RAaXFLAxjjbjT-9iK74pWteemknFkDGqGLvSOfEm HUzM130 assertion
type: Assertion
description: [Transforming growth factor-beta 1 gene polymorphisms in Korean patients with 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/20055790
was generated by: ECO_0000203

NP66705.RAR5tWy6mFNX1j3k5uWKYF7TyDW-TF1UYExrmX1PuexpY
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has publication info: NP66705.RAR5tWy6mFNX1j3k5uWKYF7TyDW-TF1UYExrmX1PuexpY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66705.RAR5tWy6mFNX1j3k5uWKYF7TyDW-TF1UYExrmX1PuexpY130 assertion
type: Assertion
description: [IL6, IL10 and TGFB1 gene polymorphisms in coeliac disease: differences between DQ2 positive and negative 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/16287542
was generated by: ECO_0000203

NP66708.RAZCTo4mvoQbn9vFiarpxcjOZGF lYcflar7t-m1ThSFA
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has publication info: NP66708.RAZCTo4mvoQbn9vFiarpxcjOZGF lYcflar7t-m1ThSFA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66708.RAZCTo4mvoQbn9vFiarpxcjOZGF lYcflar7t-m1ThSFA130 assertion
type: Assertion
description: [Genetic variants of TGFB1 and TGFBR2 genes may contribute to the risk of developing gastric cancer in an eastern Chinese population in Yixing city.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17562261
was generated by: ECO_0000203

NP66709.RAR1w7n-ybKaDJGxIhYjuIn8oGGqMjEg9ghFJqjPUhhww
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has publication info: NP66709.RAR1w7n-ybKaDJGxIhYjuIn8oGGqMjEg9ghFJqjPUhhww130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66709.RAR1w7n-ybKaDJGxIhYjuIn8oGGqMjEg9ghFJqjPUhhww130 assertion
type: Assertion
description: [The risk of dialysis access thrombosis is related to the transforming growth factor-beta1 production haplotype and is modified by polymorphisms in the plasminogen activator inhibitor-type 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/16931622
was generated by: ECO_0000203

NP66710.RAWk n-hXyMkwlVFHQrYlOy7z0UIUhdjGrqOImTC8J6KE
has assertion: NP66710.RAWk n-hXyMkwlVFHQrYlOy7z0UIUhdjGrqOImTC8J6KE130 assertion
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has publication info: NP66710.RAWk n-hXyMkwlVFHQrYlOy7z0UIUhdjGrqOImTC8J6KE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66710.RAWk n-hXyMkwlVFHQrYlOy7z0UIUhdjGrqOImTC8J6KE130 assertion
type: Assertion
description: [A pilot study of genetic polymorphisms and hemodialysis vascular access thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19210273
was generated by: ECO_0000203

NP66711.RAQe9rbCaY9iRJoqSFFbaPabo66HxDO mMcRUAec38Ovs
has assertion: NP66711.RAQe9rbCaY9iRJoqSFFbaPabo66HxDO mMcRUAec38Ovs130 assertion
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has publication info: NP66711.RAQe9rbCaY9iRJoqSFFbaPabo66HxDO mMcRUAec38Ovs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66711.RAQe9rbCaY9iRJoqSFFbaPabo66HxDO mMcRUAec38Ovs130 assertion
type: Assertion
description: [Cytokine gene polymorphisms can alter the effect of Bacillus Calmette-Gurin (BCG) immunotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16938461
was generated by: ECO_0000203

NP66712.RAVLktHgI13pm8nObu8VdJORPmTSFkc1piVX2xK-KfPDI
has assertion: NP66712.RAVLktHgI13pm8nObu8VdJORPmTSFkc1piVX2xK-KfPDI130 assertion
has provenance: NP66712.RAVLktHgI13pm8nObu8VdJORPmTSFkc1piVX2xK-KfPDI130 provenance
has publication info: NP66712.RAVLktHgI13pm8nObu8VdJORPmTSFkc1piVX2xK-KfPDI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66712.RAVLktHgI13pm8nObu8VdJORPmTSFkc1piVX2xK-KfPDI130 assertion
type: Assertion
description: [Genetic susceptibility of epidermal growth factor +61A>G and transforming growth factor beta1 -509C>T gene polymorphisms with gallbladder 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/18571008
was generated by: ECO_0000203

NP66713.RAb47Ht81QsNrRPtKXUHeEpdjOUOeCvNoUKs-SKd2iH4Q
has assertion: NP66713.RAb47Ht81QsNrRPtKXUHeEpdjOUOeCvNoUKs-SKd2iH4Q130 assertion
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has publication info: NP66713.RAb47Ht81QsNrRPtKXUHeEpdjOUOeCvNoUKs-SKd2iH4Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66713.RAb47Ht81QsNrRPtKXUHeEpdjOUOeCvNoUKs-SKd2iH4Q130 assertion
type: Assertion
description: [We aimed at analyzing whether 7 different common variants in genes coding for 2 key members of the TGF-beta signalling pathway (TGFB1 and TGFBR1) are associated with bladder cancer risk and 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/19004027
was generated by: ECO_0000203

NP66715.RAY40Gml3ReTYX-9 7F9vil689VVlAJjxC5P16QEnIs1A
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has publication info: NP66715.RAY40Gml3ReTYX-9 7F9vil689VVlAJjxC5P16QEnIs1A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66715.RAY40Gml3ReTYX-9 7F9vil689VVlAJjxC5P16QEnIs1A130 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

NP66716.RAcb-dPwaPk1a8wB8WaxqGHfkVfLoJzVzxFv6dRL5e-c8
has assertion: NP66716.RAcb-dPwaPk1a8wB8WaxqGHfkVfLoJzVzxFv6dRL5e-c8130 assertion
has provenance: NP66716.RAcb-dPwaPk1a8wB8WaxqGHfkVfLoJzVzxFv6dRL5e-c8130 provenance
has publication info: NP66716.RAcb-dPwaPk1a8wB8WaxqGHfkVfLoJzVzxFv6dRL5e-c8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66716.RAcb-dPwaPk1a8wB8WaxqGHfkVfLoJzVzxFv6dRL5e-c8130 assertion
type: Assertion
description: [The previously observed associations with risk of radiation-induced subcutaneous fibrosis could not be replicated in the present study. Further studies are needed to elucidate the influence of genetic variation upon normal tissue radiosensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16966185
was generated by: ECO_0000203

NP66719.RAUZOUwQrN4nVPlCyAb96cREfiAL GY8-aXreyR4Kty c
has assertion: NP66719.RAUZOUwQrN4nVPlCyAb96cREfiAL GY8-aXreyR4Kty c130 assertion
has provenance: NP66719.RAUZOUwQrN4nVPlCyAb96cREfiAL GY8-aXreyR4Kty c130 provenance
has publication info: NP66719.RAUZOUwQrN4nVPlCyAb96cREfiAL GY8-aXreyR4Kty c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66719.RAUZOUwQrN4nVPlCyAb96cREfiAL GY8-aXreyR4Kty c130 assertion
type: Assertion
description: [TGF-beta (-509)CC genotype may be the protective factor for the pneumoconiosis. TGF-beta (+915)GC genotype may be a susceptible factor for the pneumoconiosis. The workers of carrying TGF-beta (-509) * T and (+915) * C alleles are more susceptible to pneumoconiosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17374177
was generated by: ECO_0000203

NP66734.RAUM8aTsbxWXI-KgMG5me7kX4KCO9Ap-2hNJbcL4oKJOc
has assertion: NP66734.RAUM8aTsbxWXI-KgMG5me7kX4KCO9Ap-2hNJbcL4oKJOc130 assertion
has provenance: NP66734.RAUM8aTsbxWXI-KgMG5me7kX4KCO9Ap-2hNJbcL4oKJOc130 provenance
has publication info: NP66734.RAUM8aTsbxWXI-KgMG5me7kX4KCO9Ap-2hNJbcL4oKJOc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66734.RAUM8aTsbxWXI-KgMG5me7kX4KCO9Ap-2hNJbcL4oKJOc130 assertion
type: Assertion
description: [The polymorphism of 8570G > A in TIM4 may be associated with allergic asthma in the population of Han nationality from Hubei province 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/17407086
was generated by: ECO_0000203

NP66747.RAbNzq62DO245ZNS-YejOwca1Wn-AkZqs6SfeAzHzrT3A
has assertion: NP66747.RAbNzq62DO245ZNS-YejOwca1Wn-AkZqs6SfeAzHzrT3A130 assertion
has provenance: NP66747.RAbNzq62DO245ZNS-YejOwca1Wn-AkZqs6SfeAzHzrT3A130 provenance
has publication info: NP66747.RAbNzq62DO245ZNS-YejOwca1Wn-AkZqs6SfeAzHzrT3A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66747.RAbNzq62DO245ZNS-YejOwca1Wn-AkZqs6SfeAzHzrT3A130 assertion
type: Assertion
description: [Our results showed that SNPs in the TLR2, 4 and 9 genes were not significantly associated with susceptibility to 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/19796535
was generated by: ECO_0000203

NP66749.RAaNUGVPIUQCOxOTkv8Wnh2j7tb1dAAvdEesBxF hmuag
has assertion: NP66749.RAaNUGVPIUQCOxOTkv8Wnh2j7tb1dAAvdEesBxF hmuag130 assertion
has provenance: NP66749.RAaNUGVPIUQCOxOTkv8Wnh2j7tb1dAAvdEesBxF hmuag130 provenance
has publication info: NP66749.RAaNUGVPIUQCOxOTkv8Wnh2j7tb1dAAvdEesBxF hmuag130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66749.RAaNUGVPIUQCOxOTkv8Wnh2j7tb1dAAvdEesBxF hmuag130 assertion
type: Assertion
description: [Lack of Toll-like receptor 4 and 2 polymorphisms in Korean patients with bacteremia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17179672
was generated by: ECO_0000203

NP66753.RAdi93 p75WtYp6-AeT0fL5UN6Io49em YtHS8uA5KMPA
has assertion: NP66753.RAdi93 p75WtYp6-AeT0fL5UN6Io49em YtHS8uA5KMPA130 assertion
has provenance: NP66753.RAdi93 p75WtYp6-AeT0fL5UN6Io49em YtHS8uA5KMPA130 provenance
has publication info: NP66753.RAdi93 p75WtYp6-AeT0fL5UN6Io49em YtHS8uA5KMPA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66753.RAdi93 p75WtYp6-AeT0fL5UN6Io49em YtHS8uA5KMPA130 assertion
type: Assertion
description: [Genetic polymorphisms of CD14 and Toll-like receptor-2 (TLR2) in patients with ulcerative colitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17565650
was generated by: ECO_0000203

NP66755.RAb9-xA0S34wqfdpw-pPoNpKSUlH4JBLN7660I72f3wu0
has assertion: NP66755.RAb9-xA0S34wqfdpw-pPoNpKSUlH4JBLN7660I72f3wu0130 assertion
has provenance: NP66755.RAb9-xA0S34wqfdpw-pPoNpKSUlH4JBLN7660I72f3wu0130 provenance
has publication info: NP66755.RAb9-xA0S34wqfdpw-pPoNpKSUlH4JBLN7660I72f3wu0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66755.RAb9-xA0S34wqfdpw-pPoNpKSUlH4JBLN7660I72f3wu0130 assertion
type: Assertion
description: [Our results rather point to another as yet unidentified variant within or close to TLR4 that might confer susceptibility to 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/18422738
was generated by: ECO_0000203

NP66756.RAWgO8CthxOI0n6tToOXH6qKWbC8gzElZkqd-k9Ymv1tY
has assertion: NP66756.RAWgO8CthxOI0n6tToOXH6qKWbC8gzElZkqd-k9Ymv1tY130 assertion
has provenance: NP66756.RAWgO8CthxOI0n6tToOXH6qKWbC8gzElZkqd-k9Ymv1tY130 provenance
has publication info: NP66756.RAWgO8CthxOI0n6tToOXH6qKWbC8gzElZkqd-k9Ymv1tY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66756.RAWgO8CthxOI0n6tToOXH6qKWbC8gzElZkqd-k9Ymv1tY130 assertion
type: Assertion
description: [Association of TLR4 single-nucleotide polymorphisms and sarcoidosis in Greek 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/19839752
was generated by: ECO_0000203

NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc
has assertion: NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130 assertion
has provenance: NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130 provenance
has publication info: NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:31+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130 assertion
type: Assertion
description: [Potential reasons for absence of modifier effect include the basolateral location of TLR4 receptors on respiratory epithelium, or because inflammatory response to PA in the CF airway is so overwhelming that even a blunted response (as suggested for the 299G allele) results in increased inflammation and lung damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16830219
was generated by: ECO_0000203

NP66763.RAWdZz zhehBZ1kYsp7zrFcLOmRsLEkKeoAHVVLk oyGM
has assertion: NP66763.RAWdZz zhehBZ1kYsp7zrFcLOmRsLEkKeoAHVVLk oyGM130 assertion
has provenance: NP66763.RAWdZz zhehBZ1kYsp7zrFcLOmRsLEkKeoAHVVLk oyGM130 provenance
has publication info: NP66763.RAWdZz zhehBZ1kYsp7zrFcLOmRsLEkKeoAHVVLk oyGM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66763.RAWdZz zhehBZ1kYsp7zrFcLOmRsLEkKeoAHVVLk oyGM130 assertion
type: Assertion
description: [The possible role of TLR4 polymorphism in the outcome of severe acute pancreatitis requires further investigations in a larger series of 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/17124436
was generated by: ECO_0000203

NP66766.RAeK4nCU5ozfy-vTetpGbyuMXDTSND8wrqz108xFSD0to
has assertion: NP66766.RAeK4nCU5ozfy-vTetpGbyuMXDTSND8wrqz108xFSD0to130 assertion
has provenance: NP66766.RAeK4nCU5ozfy-vTetpGbyuMXDTSND8wrqz108xFSD0to130 provenance
has publication info: NP66766.RAeK4nCU5ozfy-vTetpGbyuMXDTSND8wrqz108xFSD0to130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66766.RAeK4nCU5ozfy-vTetpGbyuMXDTSND8wrqz108xFSD0to130 assertion
type: Assertion
description: [Toll-like receptor 4 and CD14 polymorphisms in ankylosing spondylitis: evidence of a weak association in Finns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18634146
was generated by: ECO_0000203

NP66769.RAfcoQsALLykXtrU7sFHHMI9ZjGUbk-LP8Nfv7rkt3sow
has assertion: NP66769.RAfcoQsALLykXtrU7sFHHMI9ZjGUbk-LP8Nfv7rkt3sow130 assertion
has provenance: NP66769.RAfcoQsALLykXtrU7sFHHMI9ZjGUbk-LP8Nfv7rkt3sow130 provenance
has publication info: NP66769.RAfcoQsALLykXtrU7sFHHMI9ZjGUbk-LP8Nfv7rkt3sow130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66769.RAfcoQsALLykXtrU7sFHHMI9ZjGUbk-LP8Nfv7rkt3sow130 assertion
type: Assertion
description: [Toll-like receptor (TLR) polymorphisms in African children: common TLR-4 variants predispose to 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/17373355
was generated by: ECO_0000203

NP66775.RAehizizErMM62 CNemmbog4-Jgpzs50G-S1OOaNO1Pdo
has assertion: NP66775.RAehizizErMM62 CNemmbog4-Jgpzs50G-S1OOaNO1Pdo130 assertion
has provenance: NP66775.RAehizizErMM62 CNemmbog4-Jgpzs50G-S1OOaNO1Pdo130 provenance
has publication info: NP66775.RAehizizErMM62 CNemmbog4-Jgpzs50G-S1OOaNO1Pdo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66775.RAehizizErMM62 CNemmbog4-Jgpzs50G-S1OOaNO1Pdo130 assertion
type: Assertion
description: [The G allele at position +1174 (located in intron 1 of TLR9) is closely associated with an increased risk of SLE (p = 0.029).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17344245
was generated by: ECO_0000203

NP66778.RAQnJW8zjWM6ieChD84ODlNUinhLJ7sck7pWfoUhhNGKE
has assertion: NP66778.RAQnJW8zjWM6ieChD84ODlNUinhLJ7sck7pWfoUhhNGKE130 assertion
has provenance: NP66778.RAQnJW8zjWM6ieChD84ODlNUinhLJ7sck7pWfoUhhNGKE130 provenance
has publication info: NP66778.RAQnJW8zjWM6ieChD84ODlNUinhLJ7sck7pWfoUhhNGKE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66778.RAQnJW8zjWM6ieChD84ODlNUinhLJ7sck7pWfoUhhNGKE130 assertion
type: Assertion
description: [These observations suggest that the TLR9 promoter polymorphism C-1237T might affect AE susceptibility in particular in patients with the intrinsic variant of AE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17573724
was generated by: ECO_0000203

NP66781.RAbHskdJOPJ5fXi74lIC5bKyogVCDQfdxQXCaC4nDs428
has assertion: NP66781.RAbHskdJOPJ5fXi74lIC5bKyogVCDQfdxQXCaC4nDs428130 assertion
has provenance: NP66781.RAbHskdJOPJ5fXi74lIC5bKyogVCDQfdxQXCaC4nDs428130 provenance
has publication info: NP66781.RAbHskdJOPJ5fXi74lIC5bKyogVCDQfdxQXCaC4nDs428130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
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NP66781.RAbHskdJOPJ5fXi74lIC5bKyogVCDQfdxQXCaC4nDs428130 assertion
type: Assertion
description: [A first study of cytokine genomic polymorphisms in CFS: Positive association of TNF-857 and IFNgamma 874 rare 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/16762155
was generated by: ECO_0000203

NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66782.RAWhp42qW6LWM9JM3LwogwH7hgp4w9-dw52WdA44qlaxE130 assertion
type: Assertion
description: [HLA-DQA1*0201-DQB1*0201 haplotype is involved in susceptibility, conferring 5.53 times more risk of developing this disease. EBM rating: B-2b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16890076
was generated by: ECO_0000203

NP66790.RAU7m0Z923ydjFwxmtGfUlW5mEyI-9jDDEG6vZ8ZiJTWo
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP66790.RAU7m0Z923ydjFwxmtGfUlW5mEyI-9jDDEG6vZ8ZiJTWo130 assertion
type: Assertion
description: [Polymorphisms of TNF-alpha and LT-alpha genes in multiple myeloma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18405969
was generated by: ECO_0000203

NP66793.RAewKzC2tCkQmQmjyrpmEsrDcKjM 6qIxnIGMYDP1YCPw
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP66793.RAewKzC2tCkQmQmjyrpmEsrDcKjM 6qIxnIGMYDP1YCPw130 assertion
type: Assertion
description: [This study described the haplotypic structure across a region of chromosome 6 including the tumour necrosis factor (TNF) gene, and investigated its influence on the aetiology of myeloma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15842659
was generated by: ECO_0000203

NP66795.RAfpfbHlcjH2s32u0DmVivYxjqKEAmv5u2Fb9O5fwMYjY
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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NP66795.RAfpfbHlcjH2s32u0DmVivYxjqKEAmv5u2Fb9O5fwMYjY130 assertion
type: Assertion
description: [We found that genes previously identified by their association with subclinical features of knee OA or progression were also associated with clinical knee OA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16453284
was generated by: ECO_0000203

NP66800.RAa1ivcmCvbk8RpHQ94UzYwlrQwcgkmkPsZLk7sPhnRNg
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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NP66800.RAa1ivcmCvbk8RpHQ94UzYwlrQwcgkmkPsZLk7sPhnRNg130 assertion
type: Assertion
description: [We found that genes previously identified by their association with subclinical features of knee OA or progression were also associated with clinical knee OA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16453284
was generated by: ECO_0000203

NP66803.RATb4H3OnEoMK68EC wydnpwlGMSEKkx43TeAjfSzF5io
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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version: v2.1.0.0

NP66803.RATb4H3OnEoMK68EC wydnpwlGMSEKkx43TeAjfSzF5io130 assertion
type: Assertion
description: [The association of osteoprotegerin gene polymorphisms with 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/18938269
was generated by: ECO_0000203

NP66805.RAfqypNJn01qZiIuNp6hypJ-dgmdA3MeAIRkipGvKHgr8
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP66805.RAfqypNJn01qZiIuNp6hypJ-dgmdA3MeAIRkipGvKHgr8130 assertion
type: Assertion
description: [Based on our recent finding that TACI is mutated in patients with common variable immunodeficiency, of whom more than 30% suffer from autoimmune conditions, we analyzed TACI in humans with 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/17464555
was generated by: ECO_0000203

NP66807.RASUkZQtd5duL43iMmizZKudXDuUoOLs02wO4BiP3FMfA
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66807.RASUkZQtd5duL43iMmizZKudXDuUoOLs02wO4BiP3FMfA130 assertion
type: Assertion
description: [The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16463024
was generated by: ECO_0000203

NP66816.RAXf4kucUZhiJI1QK5dMlsco04YzejGgnjW407MBNWDE8
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66816.RAXf4kucUZhiJI1QK5dMlsco04YzejGgnjW407MBNWDE8130 assertion
type: Assertion
description: [The aim of our study is to analyze whether TNF gene promoter (-308 G/A; -857 G/A) and TNF receptor polymorphisms (TNFR1 MspA1 I exon 1 and TNFR2 Nla III exon 6) show involvement in CAD predisposition in a group of Italian patients compared 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/17346438
was generated by: ECO_0000203

NP66817.RAYwOv7RBvKhcDFGMBaJXRGP TLaQwNnIlZO7ktGygVLw
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66817.RAYwOv7RBvKhcDFGMBaJXRGP TLaQwNnIlZO7ktGygVLw130 assertion
type: Assertion
description: [Our results indicate that there are genetic differences between psoriasis vulgaris patients with and without joint manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17530646
was generated by: ECO_0000203

NP66819.RAS1-Avia022zD0fX4xQD7zQLbs 2SRIjGR5cnLbG2tro
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP66819.RAS1-Avia022zD0fX4xQD7zQLbs 2SRIjGR5cnLbG2tro130 assertion
type: Assertion
description: [Prevalence and spectrum of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy 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/17101185
was generated by: ECO_0000203

NP66829.RAdDr5U9ONbcDMUHS9b3 HQynmhbYQzH4DAQ4hp0NrUlU
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66829.RAdDr5U9ONbcDMUHS9b3 HQynmhbYQzH4DAQ4hp0NrUlU130 assertion
type: Assertion
description: [The role in autism etiology of seven candidate genes in the serotonin metabolic and neurotransmission pathways and mapping to autism linkage regions (SLC6A4, HTR1A, HTR1D, HTR2A, HTR5A, TPH1 and ITGB3) was analyzed in a sample of 186 nuclear 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/17203304
was generated by: ECO_0000203

NP66831.RATvS2I6wqyP- ZtViWl3ysSQNpc1oO9pnrzWnaMumAvw
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66831.RATvS2I6wqyP- ZtViWl3ysSQNpc1oO9pnrzWnaMumAvw130 assertion
type: Assertion
description: [Family-based association study of TPH1 and TPH2 polymorphisms in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16958027
was generated by: ECO_0000203

NP66854.RASAtVStXr1T8unnfhaMqXM gIpQnWmiEo cXxmJ65SFI
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66854.RASAtVStXr1T8unnfhaMqXM gIpQnWmiEo cXxmJ65SFI130 assertion
type: Assertion
description: [Tagging single-nucleotide polymorphisms in antioxidant defense enzymes and susceptibility to 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/16424062
was generated by: ECO_0000203

NP66862.RAXMeC0jG5UJxXz15CWv55fWSz27gwL9sayKj8Do7Gp8w
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66862.RAXMeC0jG5UJxXz15CWv55fWSz27gwL9sayKj8Do7Gp8w130 assertion
type: Assertion
description: [Interactions between genes involved in the antioxidant defence system 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/16868544
was generated by: ECO_0000203

NP66863.RAS stPIqqCtpZfzdUXAVsEzNe12fWStneabScPL-Igw
has assertion: NP66863.RAS stPIqqCtpZfzdUXAVsEzNe12fWStneabScPL-Igw130 assertion
has provenance: NP66863.RAS stPIqqCtpZfzdUXAVsEzNe12fWStneabScPL-Igw130 provenance
has publication info: NP66863.RAS stPIqqCtpZfzdUXAVsEzNe12fWStneabScPL-Igw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66863.RAS stPIqqCtpZfzdUXAVsEzNe12fWStneabScPL-Igw130 assertion
type: Assertion
description: [We examined associations between 54 polymorphisms that tag the known common variants (minor allele frequency > 0.05) in 10 genes involved in oxidative damage repair (CAT, SOD1, SOD2, GPX1, GPX4, GSR, TXN, TXN2, TXNRD1, and TXNRD2) and survival in 4,470 women 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/17634480
was generated by: ECO_0000203

NP66865.RAchx5OG OgoTFffffJUUfTB5JLu9u1YY3nsbuJF5smp8
has assertion: NP66865.RAchx5OG OgoTFffffJUUfTB5JLu9u1YY3nsbuJF5smp8130 assertion
has provenance: NP66865.RAchx5OG OgoTFffffJUUfTB5JLu9u1YY3nsbuJF5smp8130 provenance
has publication info: NP66865.RAchx5OG OgoTFffffJUUfTB5JLu9u1YY3nsbuJF5smp8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66865.RAchx5OG OgoTFffffJUUfTB5JLu9u1YY3nsbuJF5smp8130 assertion
type: Assertion
description: [In this study, we evaluated the risk of acute graft-versus-host disease (GVHD) associated with genetic variation in recipient and donor MTHFR and TS genotypes to assess whether genotype alters the efficacy of MTX in acute GVHD prophylaxis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16920564
was generated by: ECO_0000203

NP66870.RAWYGdoLeovYET0TmB-K6I06EFPIX4tn6yDzSo445XBEI
has assertion: NP66870.RAWYGdoLeovYET0TmB-K6I06EFPIX4tn6yDzSo445XBEI130 assertion
has provenance: NP66870.RAWYGdoLeovYET0TmB-K6I06EFPIX4tn6yDzSo445XBEI130 provenance
has publication info: NP66870.RAWYGdoLeovYET0TmB-K6I06EFPIX4tn6yDzSo445XBEI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66870.RAWYGdoLeovYET0TmB-K6I06EFPIX4tn6yDzSo445XBEI130 assertion
type: Assertion
description: [This study examines the response to dexamethasone-doxorubicin-vincristine (DAV) therapy, followed by conditioning regimen and autologous stem cells transplantation (ASCT) in patients with multiple myeloma in relation with the presence of polymorphisms in genes involved in drug metabolism (GSTP1) and DNA synthesis (TYMS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17512053
was generated by: ECO_0000203

NP66872.RAWI6LYyNFFtLeFAH6-3WPDYPq16eBj6yN3HWDZKHyuew
has assertion: NP66872.RAWI6LYyNFFtLeFAH6-3WPDYPq16eBj6yN3HWDZKHyuew130 assertion
has provenance: NP66872.RAWI6LYyNFFtLeFAH6-3WPDYPq16eBj6yN3HWDZKHyuew130 provenance
has publication info: NP66872.RAWI6LYyNFFtLeFAH6-3WPDYPq16eBj6yN3HWDZKHyuew130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66872.RAWI6LYyNFFtLeFAH6-3WPDYPq16eBj6yN3HWDZKHyuew130 assertion
type: Assertion
description: [Polymorphisms of methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), and thymidylate synthase (TYMS) in multiple myeloma 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/17655928
was generated by: ECO_0000203

NP66874.RAewp6652BONn7htPOQ010psTo4UP7MNoNdYee7WCS0lU
has assertion: NP66874.RAewp6652BONn7htPOQ010psTo4UP7MNoNdYee7WCS0lU130 assertion
has provenance: NP66874.RAewp6652BONn7htPOQ010psTo4UP7MNoNdYee7WCS0lU130 provenance
has publication info: NP66874.RAewp6652BONn7htPOQ010psTo4UP7MNoNdYee7WCS0lU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66874.RAewp6652BONn7htPOQ010psTo4UP7MNoNdYee7WCS0lU130 assertion
type: Assertion
description: [Since a substitution of serine by tyrosine at codon 18, exon 3 (S18Y polymorphism) of the UCH-L1 gene exhibits a protective effect against the development of degenerative disease such as sporadic Parkinson's disease (PD) in several different ethnic groups, we hypothesized that UCH-L1 gene S18Y polymorphism may have that same effect on the pathologic process 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/16626667
was generated by: ECO_0000203

NP66880.RAT4CDq GOQ6v0wiJUh7oDI5Rp-ab2E1LikGs9itWeKzY
has assertion: NP66880.RAT4CDq GOQ6v0wiJUh7oDI5Rp-ab2E1LikGs9itWeKzY130 assertion
has provenance: NP66880.RAT4CDq GOQ6v0wiJUh7oDI5Rp-ab2E1LikGs9itWeKzY130 provenance
has publication info: NP66880.RAT4CDq GOQ6v0wiJUh7oDI5Rp-ab2E1LikGs9itWeKzY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66880.RAT4CDq GOQ6v0wiJUh7oDI5Rp-ab2E1LikGs9itWeKzY130 assertion
type: Assertion
description: [In conclusion, these results show the UGT2B17 deletion polymorphism 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/17387331
was generated by: ECO_0000203

NP66885.RAR6IP8WncP3W -ljkcTPEow5Gpo2ZrqCWA4QBAIYUMu8
has assertion: NP66885.RAR6IP8WncP3W -ljkcTPEow5Gpo2ZrqCWA4QBAIYUMu8130 assertion
has provenance: NP66885.RAR6IP8WncP3W -ljkcTPEow5Gpo2ZrqCWA4QBAIYUMu8130 provenance
has publication info: NP66885.RAR6IP8WncP3W -ljkcTPEow5Gpo2ZrqCWA4QBAIYUMu8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66885.RAR6IP8WncP3W -ljkcTPEow5Gpo2ZrqCWA4QBAIYUMu8130 assertion
type: Assertion
description: [our data suggested that CYP1B1 germ line-inactivating mutations might increase the incidence of HCA in women with HNF1alpha 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/17363580
was generated by: ECO_0000203

NP66895.RAX-pyk5urhorLOjNL-bi04B5mPoBipsQRVrRTTvC3bL4
has assertion: NP66895.RAX-pyk5urhorLOjNL-bi04B5mPoBipsQRVrRTTvC3bL4130 assertion
has provenance: NP66895.RAX-pyk5urhorLOjNL-bi04B5mPoBipsQRVrRTTvC3bL4130 provenance
has publication info: NP66895.RAX-pyk5urhorLOjNL-bi04B5mPoBipsQRVrRTTvC3bL4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66895.RAX-pyk5urhorLOjNL-bi04B5mPoBipsQRVrRTTvC3bL4130 assertion
type: Assertion
description: [We conducted a case-control study in a cohort of 517 PD cases and 518 ethnically matched controls to investigate the association of ubiquitin specific proteases USP24 rs487230 C>T, USP40 rs1048603 C>T, and ubiquitin thiolesterase UCHL1 rs5030732 A>C polymorphisms with the risk 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/20302855
was generated by: ECO_0000203

NP66896.RAZSC4C44NYWZedmh9hoIM4gntM0feMMqowpV7ICxNHIs
has assertion: NP66896.RAZSC4C44NYWZedmh9hoIM4gntM0feMMqowpV7ICxNHIs130 assertion
has provenance: NP66896.RAZSC4C44NYWZedmh9hoIM4gntM0feMMqowpV7ICxNHIs130 provenance
has publication info: NP66896.RAZSC4C44NYWZedmh9hoIM4gntM0feMMqowpV7ICxNHIs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66896.RAZSC4C44NYWZedmh9hoIM4gntM0feMMqowpV7ICxNHIs130 assertion
type: Assertion
description: [To assess the significance of polymorphisms of the genes for angiotensin-converting enzyme (ACE), angiotensin-converting enzyme 2 (ACE2) and urotensin II (UTS2) as risk factors for essential hypertension in two populations from north-western China, we enrolled 198 patients with essential hypertension and 131 healthy controls from the Han population and 120 patients with essential hypertension and 102 healthy controls from the Dongxiang 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/16866021
was generated by: ECO_0000203

NP66899.RAW0xsxHTfKVZgINE2VLTCJIfMlA-Q90n e37ms0KmKnc
has assertion: NP66899.RAW0xsxHTfKVZgINE2VLTCJIfMlA-Q90n e37ms0KmKnc130 assertion
has provenance: NP66899.RAW0xsxHTfKVZgINE2VLTCJIfMlA-Q90n e37ms0KmKnc130 provenance
has publication info: NP66899.RAW0xsxHTfKVZgINE2VLTCJIfMlA-Q90n e37ms0KmKnc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66899.RAW0xsxHTfKVZgINE2VLTCJIfMlA-Q90n e37ms0KmKnc130 assertion
type: Assertion
description: [SNPs in strong linkage disequilibrium and haplotypes constituting these SNPs in the versican gene are associated with IAs suggesting that variation in or near the versican gene plays a role in susceptibility to IAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16917090
was generated by: ECO_0000203

NP66901.RAb-2HNhP4AQ81Iy Doq2IGx sUExOjxTHp2ebtFckNsY
has assertion: NP66901.RAb-2HNhP4AQ81Iy Doq2IGx sUExOjxTHp2ebtFckNsY130 assertion
has provenance: NP66901.RAb-2HNhP4AQ81Iy Doq2IGx sUExOjxTHp2ebtFckNsY130 provenance
has publication info: NP66901.RAb-2HNhP4AQ81Iy Doq2IGx sUExOjxTHp2ebtFckNsY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66901.RAb-2HNhP4AQ81Iy Doq2IGx sUExOjxTHp2ebtFckNsY130 assertion
type: Assertion
description: [To determine whether -Taq I T/C and -Fok I C/T polymorphisms of vitamin D receptor (VDR) gene are associated with the familial aggregation of hepatitis B virus (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/16733893
was generated by: ECO_0000203

NP66902.RAVR2T69n 51jspOIynWrC1LaP4Y4jDcdN-dbnkIm0obM
has assertion: NP66902.RAVR2T69n 51jspOIynWrC1LaP4Y4jDcdN-dbnkIm0obM130 assertion
has provenance: NP66902.RAVR2T69n 51jspOIynWrC1LaP4Y4jDcdN-dbnkIm0obM130 provenance
has publication info: NP66902.RAVR2T69n 51jspOIynWrC1LaP4Y4jDcdN-dbnkIm0obM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66902.RAVR2T69n 51jspOIynWrC1LaP4Y4jDcdN-dbnkIm0obM130 assertion
type: Assertion
description: [VDR gene polymorphism is probably an influence factor on the genetic susceptibility of 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/17064588
was generated by: ECO_0000203

NP66913.RATCeURm7xUdSs3vHnb4eAI0dn81fZ4HcOBunnZj4IpUE
has assertion: NP66913.RATCeURm7xUdSs3vHnb4eAI0dn81fZ4HcOBunnZj4IpUE130 assertion
has provenance: NP66913.RATCeURm7xUdSs3vHnb4eAI0dn81fZ4HcOBunnZj4IpUE130 provenance
has publication info: NP66913.RATCeURm7xUdSs3vHnb4eAI0dn81fZ4HcOBunnZj4IpUE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66913.RATCeURm7xUdSs3vHnb4eAI0dn81fZ4HcOBunnZj4IpUE130 assertion
type: Assertion
description: [Polymorphisms and clinical outcome in recurrent ovarian cancer treated with cyclophosphamide and bevacizumab.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19010874
was generated by: ECO_0000203

NP66919.RAZ73ET89bCjcPeqV550ZqiKf2IHFUZoztSFULLkwCqgY
has assertion: NP66919.RAZ73ET89bCjcPeqV550ZqiKf2IHFUZoztSFULLkwCqgY130 assertion
has provenance: NP66919.RAZ73ET89bCjcPeqV550ZqiKf2IHFUZoztSFULLkwCqgY130 provenance
has publication info: NP66919.RAZ73ET89bCjcPeqV550ZqiKf2IHFUZoztSFULLkwCqgY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66919.RAZ73ET89bCjcPeqV550ZqiKf2IHFUZoztSFULLkwCqgY130 assertion
type: Assertion
description: [VHL mutation analysis in patients with isolated central nervous system haemangioblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17264095
was generated by: ECO_0000203

NP66922.RAfUX6uL P5rG5qA-N3zdnkjha4xuAVK1932Auvd9jIwQ
has assertion: NP66922.RAfUX6uL P5rG5qA-N3zdnkjha4xuAVK1932Auvd9jIwQ130 assertion
has provenance: NP66922.RAfUX6uL P5rG5qA-N3zdnkjha4xuAVK1932Auvd9jIwQ130 provenance
has publication info: NP66922.RAfUX6uL P5rG5qA-N3zdnkjha4xuAVK1932Auvd9jIwQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66922.RAfUX6uL P5rG5qA-N3zdnkjha4xuAVK1932Auvd9jIwQ130 assertion
type: Assertion
description: [Association study of sporadic Parkinson's disease genetic risk factors in patients from Russia by APEX technology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16876316
was generated by: ECO_0000203

NP66923.RAebBrDIC7CyKZLZpEqbVJQl0Bwd3xNtBJ9hvtEH9CIeY
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP66923.RAebBrDIC7CyKZLZpEqbVJQl0Bwd3xNtBJ9hvtEH9CIeY130 assertion
type: Assertion
description: [Association of a single nucleotide polymorphism in the WISP1 gene with spinal osteoarthritis in postmenopausal Japanese 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/17593496
was generated by: ECO_0000203

NP66928.RAUzKlEQ9mzXGpwIoNxyyug9cjobEjtX4k gGWME4PSlk
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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NP66928.RAUzKlEQ9mzXGpwIoNxyyug9cjobEjtX4k gGWME4PSlk130 assertion
type: Assertion
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was generated by: ECO_0000203

NP66929.RAYQIuZEdHY NRWlEt0J1vOomwuowjHpHNcSs1Y2zK8-0
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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NP66929.RAYQIuZEdHY NRWlEt0J1vOomwuowjHpHNcSs1Y2zK8-0130 assertion
type: Assertion
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NP66930.RAcGm2Jt0acc4YNqnwnYg5tqUjmpNNhbtq-j82kHHPYqE
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NP66930.RAcGm2Jt0acc4YNqnwnYg5tqUjmpNNhbtq-j82kHHPYqE130 assertion
type: Assertion
description: [To test whether genetic variations in WT1 and WIT1 (gene immediately 5' to WT1) associate with focal segmental glomerulosclerosis (FSGS), patients with biopsy-proven idiopathic and HIV-1-associated FSGS were enrolled in a multicenter study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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SIO_000772: http://identifiers.org/pubmed/15687485
was generated by: ECO_0000203

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type: Nanopublication
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NP66931.RAZUlFNrwh8qu24mDpwJzVSaTx64HJDvKPZLynZEsjj1k130 assertion
type: Assertion
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NP66945.RAQCiG5or5gLfKNJM8t6pLCtMA3lTdn8hIhBEaWoYfx6g
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type: Nanopublication
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version: v2.1.0.0

NP66945.RAQCiG5or5gLfKNJM8t6pLCtMA3lTdn8hIhBEaWoYfx6g130 assertion
type: Assertion
description: [Pharmacogenetic approach for capecitabine or 5-fluorouracil selection to be combined with oxaliplatin as first-line chemotherapy in advanced colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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NP66947.RASP9kloJZ84BLQNlglEyTqWqbxO5z uDQP5Hb6khme60
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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NP66947.RASP9kloJZ84BLQNlglEyTqWqbxO5z uDQP5Hb6khme60130 assertion
type: Assertion
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NP66959.RAW3XXfXRxIQrmjzHUMQ5jz3axj8EWQRdyVj5HVx7Hbqs
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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NP66959.RAW3XXfXRxIQrmjzHUMQ5jz3axj8EWQRdyVj5HVx7Hbqs130 assertion
type: Assertion
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SIO_000772: http://identifiers.org/pubmed/19692168
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NP66961.RAfV7po1MzacguEUsjF9yIGVrJBf 1IVP6nrlH6XZWF3E
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type: Nanopublication
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subject: SIO_000983
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NP66961.RAfV7po1MzacguEUsjF9yIGVrJBf 1IVP6nrlH6XZWF3E130 assertion
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NP66962.RATtDQkYoFl7lHWDlGxmxUozAgwTadnOrm7skhl4Q7Xko
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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version: v2.1.0.0

NP66962.RATtDQkYoFl7lHWDlGxmxUozAgwTadnOrm7skhl4Q7Xko130 assertion
type: Assertion
description: [genetic variants of the genes involved in the DSB repair pathway may play a role in the etiology of glioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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SIO_000772: http://identifiers.org/pubmed/17389609
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NP66969.RAZye8nJlmt2xVWXCAjT6l77AjYHoYh1zdaHppXjt03Qs
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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subject: SIO_000983
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version: v2.1.0.0

NP66969.RAZye8nJlmt2xVWXCAjT6l77AjYHoYh1zdaHppXjt03Qs130 assertion
type: Assertion
description: [Our study shows that AT1R and AT2R are expressed locally in gastric cancer and that the combination of AT1R expression and ACE I/D gene polymorphism correlates with nodal spread in intestinal type 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/17548686
was generated by: ECO_0000203

NP66973.RAQV4-vVtzZoFpDuz3nONL3y6nfAdJPlBHCGA yY VikQ
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66973.RAQV4-vVtzZoFpDuz3nONL3y6nfAdJPlBHCGA yY VikQ130 assertion
type: Assertion
description: [Platelet glycoprotein Ia 807C/T and 873G/A polymorphisms in patients with venous thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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SIO_000772: http://identifiers.org/pubmed/17164499
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NP66975.RAZUzGfnJbRVVnvYF8MavsSQRSK69aRK2EfB6elzjNG7Q
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66975.RAZUzGfnJbRVVnvYF8MavsSQRSK69aRK2EfB6elzjNG7Q130 assertion
type: Assertion
description: [The Leu33Pro polymorphism in the ITGB3 gene does not modify BRCA1/2-associated breast or ovarian cancer risks: results from a multicenter study among 15,542 BRCA1 and BRCA2 mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
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was generated by: ECO_0000203

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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP66977.RAUnyHr5n1A9WNGI98c1WqFYDBQukKFy9wTIEfQipYu6U130 assertion
type: Assertion
description: [this study suggests that the activating KIR2DS4 may serve as CML susceptive gene to trigger leukemia development, while KIR2DS3 is possibly a protect gene of ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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was generated by: ECO_0000203

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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP66978.RAWIZDtFOv39p31eImyMJZ48Ui6skmjw1mspGNrp4B80g130 assertion
type: Assertion
description: [In this study, a functional polymorphism in the 5' flanking region of the leptin gene (LEP -2548 G/A) was found to increase susceptibility for non-small cell lung cancer odds ratio (OR), 1.97; 95% confidence interval (CI), 1.13-3.43.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16630717
was generated by: ECO_0000203

NP66982.RAQiwQRFqsv8ehupwe0vflRNaT2kPgoWmKg 1wWfvuRfI
has assertion: NP66982.RAQiwQRFqsv8ehupwe0vflRNaT2kPgoWmKg 1wWfvuRfI130 assertion
has provenance: NP66982.RAQiwQRFqsv8ehupwe0vflRNaT2kPgoWmKg 1wWfvuRfI130 provenance
has publication info: NP66982.RAQiwQRFqsv8ehupwe0vflRNaT2kPgoWmKg 1wWfvuRfI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66982.RAQiwQRFqsv8ehupwe0vflRNaT2kPgoWmKg 1wWfvuRfI130 assertion
type: Assertion
description: [Assessment of the toll-like receptor 4 Asp299Gly, Thr399Ile and interleukin-8 -251 polymorphisms in the risk for the development of distal 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/17462092
was generated by: ECO_0000203

NP66984.RAbgPwHpbQlejBJGtcmIV8UIbito-N0QpUrtHJVABZwAQ
has assertion: NP66984.RAbgPwHpbQlejBJGtcmIV8UIbito-N0QpUrtHJVABZwAQ130 assertion
has provenance: NP66984.RAbgPwHpbQlejBJGtcmIV8UIbito-N0QpUrtHJVABZwAQ130 provenance
has publication info: NP66984.RAbgPwHpbQlejBJGtcmIV8UIbito-N0QpUrtHJVABZwAQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66984.RAbgPwHpbQlejBJGtcmIV8UIbito-N0QpUrtHJVABZwAQ130 assertion
type: Assertion
description: [Tag polymorphisms at the A20 (TNFAIP3) locus are associated with lower gene expression and increased risk of coronary artery disease in 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/17259397
was generated by: ECO_0000203

NP66986.RAWIc7im6LREL2y3Wg0BgcKyHCFkLkc1gdscg44RnYSxk
has assertion: NP66986.RAWIc7im6LREL2y3Wg0BgcKyHCFkLkc1gdscg44RnYSxk130 assertion
has provenance: NP66986.RAWIc7im6LREL2y3Wg0BgcKyHCFkLkc1gdscg44RnYSxk130 provenance
has publication info: NP66986.RAWIc7im6LREL2y3Wg0BgcKyHCFkLkc1gdscg44RnYSxk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66986.RAWIc7im6LREL2y3Wg0BgcKyHCFkLkc1gdscg44RnYSxk130 assertion
type: Assertion
description: [We evaluated the frequency of ABCB1 polymorphisms (2677G/T>A and 3435C>T) and studied the association between the polymorphisms and clinical outcomes of paclitaxel-based chemotherapy in advanced gastric 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/19956892
was generated by: ECO_0000203

NP66992.RAcD8QudaqVZOGWIZ2l5SMKvLoheW7AE53Knp4FepAYyU
has assertion: NP66992.RAcD8QudaqVZOGWIZ2l5SMKvLoheW7AE53Knp4FepAYyU130 assertion
has provenance: NP66992.RAcD8QudaqVZOGWIZ2l5SMKvLoheW7AE53Knp4FepAYyU130 provenance
has publication info: NP66992.RAcD8QudaqVZOGWIZ2l5SMKvLoheW7AE53Knp4FepAYyU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP66992.RAcD8QudaqVZOGWIZ2l5SMKvLoheW7AE53Knp4FepAYyU130 assertion
type: Assertion
description: [Investigation of GSTT1, GSTM1 and NQO1 genes polymorphisms in myelodysplastic 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/16620556
was generated by: ECO_0000203

NP67004.RAapXrLQMrIvsd6nmAYi5EFIzgsOFNBPd7oVrp6MmUrgc
has assertion: NP67004.RAapXrLQMrIvsd6nmAYi5EFIzgsOFNBPd7oVrp6MmUrgc130 assertion
has provenance: NP67004.RAapXrLQMrIvsd6nmAYi5EFIzgsOFNBPd7oVrp6MmUrgc130 provenance
has publication info: NP67004.RAapXrLQMrIvsd6nmAYi5EFIzgsOFNBPd7oVrp6MmUrgc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67004.RAapXrLQMrIvsd6nmAYi5EFIzgsOFNBPd7oVrp6MmUrgc130 assertion
type: Assertion
description: [ADH1C genotype modifies the association between alcohol consumption and 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/17563066
was generated by: ECO_0000203

NP67007.RATD6CalttHwrUJsv8sU2xB5ssdjvbnok0yPBdDIiD 7E
has assertion: NP67007.RATD6CalttHwrUJsv8sU2xB5ssdjvbnok0yPBdDIiD 7E130 assertion
has provenance: NP67007.RATD6CalttHwrUJsv8sU2xB5ssdjvbnok0yPBdDIiD 7E130 provenance
has publication info: NP67007.RATD6CalttHwrUJsv8sU2xB5ssdjvbnok0yPBdDIiD 7E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67007.RATD6CalttHwrUJsv8sU2xB5ssdjvbnok0yPBdDIiD 7E130 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

NP67011.RAcMDxU8zHR-kaSAT99qnXrd2q7-DokbEUg4ZbUesjr-8
has assertion: NP67011.RAcMDxU8zHR-kaSAT99qnXrd2q7-DokbEUg4ZbUesjr-8130 assertion
has provenance: NP67011.RAcMDxU8zHR-kaSAT99qnXrd2q7-DokbEUg4ZbUesjr-8130 provenance
has publication info: NP67011.RAcMDxU8zHR-kaSAT99qnXrd2q7-DokbEUg4ZbUesjr-8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67011.RAcMDxU8zHR-kaSAT99qnXrd2q7-DokbEUg4ZbUesjr-8130 assertion
type: Assertion
description: [Overall, APOC3 promoter variants were associated with a greater likelihood of MetS compared to wild type C-482T (OR: 4.3; 95% CI: 2.2, 8.6 p <0.0001), T-455C (OR: 3.6; 95% CI: 2.0, 6.7 p <0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17416293
was generated by: ECO_0000203

NP67012.RAbVhxPd9dDvZQUeOTWqZZv07eFB659gAgCIrwXolR0bA
has assertion: NP67012.RAbVhxPd9dDvZQUeOTWqZZv07eFB659gAgCIrwXolR0bA130 assertion
has provenance: NP67012.RAbVhxPd9dDvZQUeOTWqZZv07eFB659gAgCIrwXolR0bA130 provenance
has publication info: NP67012.RAbVhxPd9dDvZQUeOTWqZZv07eFB659gAgCIrwXolR0bA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67012.RAbVhxPd9dDvZQUeOTWqZZv07eFB659gAgCIrwXolR0bA130 assertion
type: Assertion
description: [The APOA5 Ser19Trp, APOA5 -12,238T>C, APOA4 Thr347Ser, APOC3 -482C>T and APOC3 3238C>G (SstI) polymorphisms were analyzed in a representative population sample of 3138 men and women from France, including 932 individuals with metabolic syndrome and 2206 without metabolic syndrome, as defined by the NCEP criteria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18789138
was generated by: ECO_0000203

NP67014.RAbZIerU3c-9QZwkixoAxXzfh-dE aQa8B7foS-tkUKYk
has assertion: NP67014.RAbZIerU3c-9QZwkixoAxXzfh-dE aQa8B7foS-tkUKYk130 assertion
has provenance: NP67014.RAbZIerU3c-9QZwkixoAxXzfh-dE aQa8B7foS-tkUKYk130 provenance
has publication info: NP67014.RAbZIerU3c-9QZwkixoAxXzfh-dE aQa8B7foS-tkUKYk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67014.RAbZIerU3c-9QZwkixoAxXzfh-dE aQa8B7foS-tkUKYk130 assertion
type: Assertion
description: [ApoE epsilon2/epsilon3/epsilon4 gene polymorphism is a determinant of the relative proportion of apolipoprotein C-III to E. Carriers of the unfavourable E4 allele present the highest ApoCIII/ApoE ratio and are twofold more frequent among individuals affected by MetSyn.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18188530
was generated by: ECO_0000203

NP67016.RAY0PA32gW84xOK9cq LAPGyP72Sb3f4pfYd7cxGlgw0Y
has assertion: NP67016.RAY0PA32gW84xOK9cq LAPGyP72Sb3f4pfYd7cxGlgw0Y130 assertion
has provenance: NP67016.RAY0PA32gW84xOK9cq LAPGyP72Sb3f4pfYd7cxGlgw0Y130 provenance
has publication info: NP67016.RAY0PA32gW84xOK9cq LAPGyP72Sb3f4pfYd7cxGlgw0Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67016.RAY0PA32gW84xOK9cq LAPGyP72Sb3f4pfYd7cxGlgw0Y130 assertion
type: Assertion
description: [We replicated genetic associations for CD with IL23R, ATG16L1, IRGM, NKX2-3, 1q24, 10q21, 5p13, and PTPN2 and report evidence for associations with HERC2 and CCNY.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19174780
was generated by: ECO_0000203

NP67025.RARyCyXn3P8jKOLXucS GNi6nFIyngLO9GECzNqVhVeoA
has assertion: NP67025.RARyCyXn3P8jKOLXucS GNi6nFIyngLO9GECzNqVhVeoA130 assertion
has provenance: NP67025.RARyCyXn3P8jKOLXucS GNi6nFIyngLO9GECzNqVhVeoA130 provenance
has publication info: NP67025.RARyCyXn3P8jKOLXucS GNi6nFIyngLO9GECzNqVhVeoA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67025.RARyCyXn3P8jKOLXucS GNi6nFIyngLO9GECzNqVhVeoA130 assertion
type: Assertion
description: [Using voxel-based morphometry in 30 asymptomatic mutation carriers (MC) with mutations in four different genes for PD and 100 healthy controls, we identified an increase in gray matter volume (GMV) in the striatum in asymptomatic Parkin, PINK1, ATP13A2 and, to a much lesser extent, in LRRK2 MC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20483373
was generated by: ECO_0000203

NP67027.RAc1hmz8gSCYXvrbVukqP4Sdh 9oFwkSJih4DBfAIfvYA
has assertion: NP67027.RAc1hmz8gSCYXvrbVukqP4Sdh 9oFwkSJih4DBfAIfvYA130 assertion
has provenance: NP67027.RAc1hmz8gSCYXvrbVukqP4Sdh 9oFwkSJih4DBfAIfvYA130 provenance
has publication info: NP67027.RAc1hmz8gSCYXvrbVukqP4Sdh 9oFwkSJih4DBfAIfvYA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67027.RAc1hmz8gSCYXvrbVukqP4Sdh 9oFwkSJih4DBfAIfvYA130 assertion
type: Assertion
description: [We confirm that ATP13A2 homozygous mutations are associated with human parkinsonism, and expand the associated genotypic and clinical spectrum, by describing a homozygous missense mutation in this gene in a patient with a phenotype milder than that initially associated with ATP13A2 mutations (Kufor-Rakeb 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/17485642
was generated by: ECO_0000203

NP67028.RAe-HCeEh7JP7ua8OtEFV ZTEpo2qvUAY6nk4Pd3hY2x4
has assertion: NP67028.RAe-HCeEh7JP7ua8OtEFV ZTEpo2qvUAY6nk4Pd3hY2x4130 assertion
has provenance: NP67028.RAe-HCeEh7JP7ua8OtEFV ZTEpo2qvUAY6nk4Pd3hY2x4130 provenance
has publication info: NP67028.RAe-HCeEh7JP7ua8OtEFV ZTEpo2qvUAY6nk4Pd3hY2x4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67028.RAe-HCeEh7JP7ua8OtEFV ZTEpo2qvUAY6nk4Pd3hY2x4130 assertion
type: Assertion
description: [on roles of ATP13A2 variant in Asians or other 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/20976737
was generated by: ECO_0000203

NP67031.RAdTcOVkF2lDFBFRAAGJ6QuCMhanfB3RSaplhigTawQ38
has assertion: NP67031.RAdTcOVkF2lDFBFRAAGJ6QuCMhanfB3RSaplhigTawQ38130 assertion
has provenance: NP67031.RAdTcOVkF2lDFBFRAAGJ6QuCMhanfB3RSaplhigTawQ38130 provenance
has publication info: NP67031.RAdTcOVkF2lDFBFRAAGJ6QuCMhanfB3RSaplhigTawQ38130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67031.RAdTcOVkF2lDFBFRAAGJ6QuCMhanfB3RSaplhigTawQ38130 assertion
type: Assertion
description: [Mutation analysis of ATP13A2 gene in Chinese patients with familial autosomal recessive early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19806583
was generated by: ECO_0000203

NP67033.RARSiuaC8rvSL1M-4jPcDDgZ1poA w34QbLQ-GOLtmJYc
has assertion: NP67033.RARSiuaC8rvSL1M-4jPcDDgZ1poA w34QbLQ-GOLtmJYc130 assertion
has provenance: NP67033.RARSiuaC8rvSL1M-4jPcDDgZ1poA w34QbLQ-GOLtmJYc130 provenance
has publication info: NP67033.RARSiuaC8rvSL1M-4jPcDDgZ1poA w34QbLQ-GOLtmJYc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67033.RARSiuaC8rvSL1M-4jPcDDgZ1poA w34QbLQ-GOLtmJYc130 assertion
type: Assertion
description: [Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic 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/19224617
was generated by: ECO_0000203

NP67035.RAZEvLPCT2tbdsRUTWN0lzt4UmriwstweHhXbbRdw1ZrA
has assertion: NP67035.RAZEvLPCT2tbdsRUTWN0lzt4UmriwstweHhXbbRdw1ZrA130 assertion
has provenance: NP67035.RAZEvLPCT2tbdsRUTWN0lzt4UmriwstweHhXbbRdw1ZrA130 provenance
has publication info: NP67035.RAZEvLPCT2tbdsRUTWN0lzt4UmriwstweHhXbbRdw1ZrA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67035.RAZEvLPCT2tbdsRUTWN0lzt4UmriwstweHhXbbRdw1ZrA130 assertion
type: Assertion
description: [Association of candidate susceptible loci with chronic infection with hepatitis B virus 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/20087947
was generated by: ECO_0000203

NP67043.RAbCgiQTjQyGeWkAo0QOfmrhpNyougw1R4qMuV8ml MIE
has assertion: NP67043.RAbCgiQTjQyGeWkAo0QOfmrhpNyougw1R4qMuV8ml MIE130 assertion
has provenance: NP67043.RAbCgiQTjQyGeWkAo0QOfmrhpNyougw1R4qMuV8ml MIE130 provenance
has publication info: NP67043.RAbCgiQTjQyGeWkAo0QOfmrhpNyougw1R4qMuV8ml MIE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67043.RAbCgiQTjQyGeWkAo0QOfmrhpNyougw1R4qMuV8ml MIE130 assertion
type: Assertion
description: [Metabolic gene variants 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/16985026
was generated by: ECO_0000203

NP67044.RAQalo04AhnGahw5v43nmSH5H Sgfjv0eoiRQTekoIESE
has assertion: NP67044.RAQalo04AhnGahw5v43nmSH5H Sgfjv0eoiRQTekoIESE130 assertion
has provenance: NP67044.RAQalo04AhnGahw5v43nmSH5H Sgfjv0eoiRQTekoIESE130 provenance
has publication info: NP67044.RAQalo04AhnGahw5v43nmSH5H Sgfjv0eoiRQTekoIESE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67044.RAQalo04AhnGahw5v43nmSH5H Sgfjv0eoiRQTekoIESE130 assertion
type: Assertion
description: [Genetic variations in xenobiotic metabolic pathway genes, personal hair dye use, and risk of 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/19822571
was generated by: ECO_0000203

NP67048.RARbVgWBJLHJOJfqNoapchz7lzxqwJ0prPFgTxrO5v1n4
has assertion: NP67048.RARbVgWBJLHJOJfqNoapchz7lzxqwJ0prPFgTxrO5v1n4130 assertion
has provenance: NP67048.RARbVgWBJLHJOJfqNoapchz7lzxqwJ0prPFgTxrO5v1n4130 provenance
has publication info: NP67048.RARbVgWBJLHJOJfqNoapchz7lzxqwJ0prPFgTxrO5v1n4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67048.RARbVgWBJLHJOJfqNoapchz7lzxqwJ0prPFgTxrO5v1n4130 assertion
type: Assertion
description: [SNPs in four genes (ERCC5, ERCC2, WRN, and BRCA1) were associated with altered risk of NHL and diffuse large B-cell lymphoma (DLBCL), the major B cell subtype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16738949
was generated by: ECO_0000203

NP67050.RATQ36FkbOOEQMgwZzl3DDacVe8bljG1QWq-NtmNAt4RM
has assertion: NP67050.RATQ36FkbOOEQMgwZzl3DDacVe8bljG1QWq-NtmNAt4RM130 assertion
has provenance: NP67050.RATQ36FkbOOEQMgwZzl3DDacVe8bljG1QWq-NtmNAt4RM130 provenance
has publication info: NP67050.RATQ36FkbOOEQMgwZzl3DDacVe8bljG1QWq-NtmNAt4RM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67050.RATQ36FkbOOEQMgwZzl3DDacVe8bljG1QWq-NtmNAt4RM130 assertion
type: Assertion
description: [Association of gene polymorphisms in the DNA repair gene XPD with 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/18315909
was generated by: ECO_0000203

NP67055.RAXCM42rptL8q0Fmz5eWhyObWwFWxkkpqQEpUb0N7z4G0
has assertion: NP67055.RAXCM42rptL8q0Fmz5eWhyObWwFWxkkpqQEpUb0N7z4G0130 assertion
has provenance: NP67055.RAXCM42rptL8q0Fmz5eWhyObWwFWxkkpqQEpUb0N7z4G0130 provenance
has publication info: NP67055.RAXCM42rptL8q0Fmz5eWhyObWwFWxkkpqQEpUb0N7z4G0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67055.RAXCM42rptL8q0Fmz5eWhyObWwFWxkkpqQEpUb0N7z4G0130 assertion
type: Assertion
description: [Our study shows that factor V Leiden mutation, and investigated platelet GP Ia, and GP IIIa polymorphisms frequently coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16875034
was generated by: ECO_0000203

NP67059.RAY6TJp1-RF7ctO TGkMzu7dTgPfypeFu958G-TDrStcs
has assertion: NP67059.RAY6TJp1-RF7ctO TGkMzu7dTgPfypeFu958G-TDrStcs130 assertion
has provenance: NP67059.RAY6TJp1-RF7ctO TGkMzu7dTgPfypeFu958G-TDrStcs130 provenance
has publication info: NP67059.RAY6TJp1-RF7ctO TGkMzu7dTgPfypeFu958G-TDrStcs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67059.RAY6TJp1-RF7ctO TGkMzu7dTgPfypeFu958G-TDrStcs130 assertion
type: Assertion
description: [Varied prevalence of factor V G1691A (Leiden) and prothrombin G20210A single nucleotide polymorphisms among Arabs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16261289
was generated by: ECO_0000203

NP67065.RAXMjKLQx0OCTsSXfvgsDDShbW3feF8IWPVgPIFROumXQ
has assertion: NP67065.RAXMjKLQx0OCTsSXfvgsDDShbW3feF8IWPVgPIFROumXQ130 assertion
has provenance: NP67065.RAXMjKLQx0OCTsSXfvgsDDShbW3feF8IWPVgPIFROumXQ130 provenance
has publication info: NP67065.RAXMjKLQx0OCTsSXfvgsDDShbW3feF8IWPVgPIFROumXQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67065.RAXMjKLQx0OCTsSXfvgsDDShbW3feF8IWPVgPIFROumXQ130 assertion
type: Assertion
description: [Functional evidence suggests that the 001Msp, fcrl3_3, fcrl3_5, and fcrl3_6 SNPs could cause changes in B cell signaling and activation pathways that could account for their association with GD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16384851
was generated by: ECO_0000203

NP67074.RAanZNtWKL3LSZ1rsNjR feRDANR8xgLwNEfPw60TELVM
has assertion: NP67074.RAanZNtWKL3LSZ1rsNjR feRDANR8xgLwNEfPw60TELVM130 assertion
has provenance: NP67074.RAanZNtWKL3LSZ1rsNjR feRDANR8xgLwNEfPw60TELVM130 provenance
has publication info: NP67074.RAanZNtWKL3LSZ1rsNjR feRDANR8xgLwNEfPw60TELVM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67074.RAanZNtWKL3LSZ1rsNjR feRDANR8xgLwNEfPw60TELVM130 assertion
type: Assertion
description: [The -5T/C polymorphism of the platelet glycoprotein GPIb alpha Kozak gene is implicated in the pathogenesis of TIA. C allele is an independent risk factor for TIA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17029210
was generated by: ECO_0000203

NP67081.RAQm-glZqcXgxWi8BK55Si1kGsiYyBdv7UuAb0OD9qah0
has assertion: NP67081.RAQm-glZqcXgxWi8BK55Si1kGsiYyBdv7UuAb0OD9qah0130 assertion
has provenance: NP67081.RAQm-glZqcXgxWi8BK55Si1kGsiYyBdv7UuAb0OD9qah0130 provenance
has publication info: NP67081.RAQm-glZqcXgxWi8BK55Si1kGsiYyBdv7UuAb0OD9qah0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67081.RAQm-glZqcXgxWi8BK55Si1kGsiYyBdv7UuAb0OD9qah0130 assertion
type: Assertion
description: [HLA and MICA associations with head and neck squamous 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/16857416
was generated by: ECO_0000203

NP67086.RAVBQd7b9Vv ux0PSIy6xCfqZmnfwxemnMR4VRwg1mxGw
has assertion: NP67086.RAVBQd7b9Vv ux0PSIy6xCfqZmnfwxemnMR4VRwg1mxGw130 assertion
has provenance: NP67086.RAVBQd7b9Vv ux0PSIy6xCfqZmnfwxemnMR4VRwg1mxGw130 provenance
has publication info: NP67086.RAVBQd7b9Vv ux0PSIy6xCfqZmnfwxemnMR4VRwg1mxGw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67086.RAVBQd7b9Vv ux0PSIy6xCfqZmnfwxemnMR4VRwg1mxGw130 assertion
type: Assertion
description: [A non-synonymous single nucleotide polymorphism in IFNAR1 affects susceptibility to chronic 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/18761606
was generated by: ECO_0000203

NP67091.RAXXz-uX49U6SSxJOk7xlheFRybhFyBjFk7Uj1Kib7F5c
has assertion: NP67091.RAXXz-uX49U6SSxJOk7xlheFRybhFyBjFk7Uj1Kib7F5c130 assertion
has provenance: NP67091.RAXXz-uX49U6SSxJOk7xlheFRybhFyBjFk7Uj1Kib7F5c130 provenance
has publication info: NP67091.RAXXz-uX49U6SSxJOk7xlheFRybhFyBjFk7Uj1Kib7F5c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67091.RAXXz-uX49U6SSxJOk7xlheFRybhFyBjFk7Uj1Kib7F5c130 assertion
type: Assertion
description: [Cytokine gene polymorphisms can alter the effect of Bacillus Calmette-Gurin (BCG) immunotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16938461
was generated by: ECO_0000203

NP67092.RARS1MOxHh0uLeL6vcLNCdbv9f-Aj-Uf9Q6q0Pb5Jz8Kg
has assertion: NP67092.RARS1MOxHh0uLeL6vcLNCdbv9f-Aj-Uf9Q6q0Pb5Jz8Kg130 assertion
has provenance: NP67092.RARS1MOxHh0uLeL6vcLNCdbv9f-Aj-Uf9Q6q0Pb5Jz8Kg130 provenance
has publication info: NP67092.RARS1MOxHh0uLeL6vcLNCdbv9f-Aj-Uf9Q6q0Pb5Jz8Kg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67092.RARS1MOxHh0uLeL6vcLNCdbv9f-Aj-Uf9Q6q0Pb5Jz8Kg130 assertion
type: Assertion
description: [IL-1 gene polymorphisms and genetic susceptibility of gallbladder cancer in a north Indian 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/18940468
was generated by: ECO_0000203

NP67096.RAdJFQUQbbAdqfVnYx8x KWm gznWNB3rqNmObuGDUBbA
has assertion: NP67096.RAdJFQUQbbAdqfVnYx8x KWm gznWNB3rqNmObuGDUBbA130 assertion
has provenance: NP67096.RAdJFQUQbbAdqfVnYx8x KWm gznWNB3rqNmObuGDUBbA130 provenance
has publication info: NP67096.RAdJFQUQbbAdqfVnYx8x KWm gznWNB3rqNmObuGDUBbA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67096.RAdJFQUQbbAdqfVnYx8x KWm gznWNB3rqNmObuGDUBbA130 assertion
type: Assertion
description: [Association between human African trypanosomiasis and the IL6 gene in a Congolese 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/16720107
was generated by: ECO_0000203

NP67102.RAdj6IrBtmB16ZMVhU7UOI43sCjeSF6POOCL3ce0zL0U8
has assertion: NP67102.RAdj6IrBtmB16ZMVhU7UOI43sCjeSF6POOCL3ce0zL0U8130 assertion
has provenance: NP67102.RAdj6IrBtmB16ZMVhU7UOI43sCjeSF6POOCL3ce0zL0U8130 provenance
has publication info: NP67102.RAdj6IrBtmB16ZMVhU7UOI43sCjeSF6POOCL3ce0zL0U8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67102.RAdj6IrBtmB16ZMVhU7UOI43sCjeSF6POOCL3ce0zL0U8130 assertion
type: Assertion
description: [Using Phase II HapMap data, we demonstrate that there are a set of polymorphisms, spanning genes from prolyl 4-hydroxylase (P4HA2) through interferon regulatory factor 1 (IRF1) with equivalent statistical evidence of association to the reported SLC22A4 variant and that each, by itself, could entirely explain the IBD5 association to 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/17213842
was generated by: ECO_0000203

NP67105.RAS4riTu3MysSSEI CtFrt7P0I9rmNfjpzINyX LL9Mo
has assertion: NP67105.RAS4riTu3MysSSEI CtFrt7P0I9rmNfjpzINyX LL9Mo130 assertion
has provenance: NP67105.RAS4riTu3MysSSEI CtFrt7P0I9rmNfjpzINyX LL9Mo130 provenance
has publication info: NP67105.RAS4riTu3MysSSEI CtFrt7P0I9rmNfjpzINyX LL9Mo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67105.RAS4riTu3MysSSEI CtFrt7P0I9rmNfjpzINyX LL9Mo130 assertion
type: Assertion
description: [The prothrombotic Pl(A2) allele of platelet fibrinogen receptor GPIIb/IIIa increased the risk of metastases in RCC in 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/16831169
was generated by: ECO_0000203

NP67108.RAf9u5-WOMYiuGMmoNrfh-ePZjn0UcxsEyN9GkdmS5SXc
has assertion: NP67108.RAf9u5-WOMYiuGMmoNrfh-ePZjn0UcxsEyN9GkdmS5SXc130 assertion
has provenance: NP67108.RAf9u5-WOMYiuGMmoNrfh-ePZjn0UcxsEyN9GkdmS5SXc130 provenance
has publication info: NP67108.RAf9u5-WOMYiuGMmoNrfh-ePZjn0UcxsEyN9GkdmS5SXc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67108.RAf9u5-WOMYiuGMmoNrfh-ePZjn0UcxsEyN9GkdmS5SXc130 assertion
type: Assertion
description: [The 584C/T polymorphism of the EL gene was associated with AMI independently of HDL-C levels and thus may be involved in the pathogenesis of 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/17526978
was generated by: ECO_0000203

NP67120.RAWxpdU4bvnKXzbJtDlu4ZwfrxpQs1HG8gbCN8RD2u7KY
has assertion: NP67120.RAWxpdU4bvnKXzbJtDlu4ZwfrxpQs1HG8gbCN8RD2u7KY130 assertion
has provenance: NP67120.RAWxpdU4bvnKXzbJtDlu4ZwfrxpQs1HG8gbCN8RD2u7KY130 provenance
has publication info: NP67120.RAWxpdU4bvnKXzbJtDlu4ZwfrxpQs1HG8gbCN8RD2u7KY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67120.RAWxpdU4bvnKXzbJtDlu4ZwfrxpQs1HG8gbCN8RD2u7KY130 assertion
type: Assertion
description: [RNFL thickness was significantly increased in the early stage and decreased in the late stage in the 11778 group than in the 14484 group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19247386
was generated by: ECO_0000203

NP67121.RAQYV1BvLO8-VdF7DMeq-huTOx5gtpV6ob0WnFuEqpPPI
has assertion: NP67121.RAQYV1BvLO8-VdF7DMeq-huTOx5gtpV6ob0WnFuEqpPPI130 assertion
has provenance: NP67121.RAQYV1BvLO8-VdF7DMeq-huTOx5gtpV6ob0WnFuEqpPPI130 provenance
has publication info: NP67121.RAQYV1BvLO8-VdF7DMeq-huTOx5gtpV6ob0WnFuEqpPPI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67121.RAQYV1BvLO8-VdF7DMeq-huTOx5gtpV6ob0WnFuEqpPPI130 assertion
type: Assertion
description: [The three LHON primary mutations are rare in general Chinese populations. The optimized MAS-PCR assay provides an easier, faster and more cost-effective method for detection of the three LHON primary mutations, making it practical for clinical 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/20599858
was generated by: ECO_0000203

NP67124.RAeJvstV PdHf8ES5Wq5SMWuD3wX2GORR-x48wB4jNEss
has assertion: NP67124.RAeJvstV PdHf8ES5Wq5SMWuD3wX2GORR-x48wB4jNEss130 assertion
has provenance: NP67124.RAeJvstV PdHf8ES5Wq5SMWuD3wX2GORR-x48wB4jNEss130 provenance
has publication info: NP67124.RAeJvstV PdHf8ES5Wq5SMWuD3wX2GORR-x48wB4jNEss130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67124.RAeJvstV PdHf8ES5Wq5SMWuD3wX2GORR-x48wB4jNEss130 assertion
type: Assertion
description: [Chinese individuals >or=50 years of age carrying the AG genotype of NFKBIA may be at an increased risk of developing CRC, and the GG genotype of NFKBIA may be considered as a prognostic factor for Swedish CRC 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/17354114
was generated by: ECO_0000203

NP67130.RAb3OEq6uvHN-WMrW-sAnwbRqiXmdBpSPQDxbaAM M4T4
has assertion: NP67130.RAb3OEq6uvHN-WMrW-sAnwbRqiXmdBpSPQDxbaAM M4T4130 assertion
has provenance: NP67130.RAb3OEq6uvHN-WMrW-sAnwbRqiXmdBpSPQDxbaAM M4T4130 provenance
has publication info: NP67130.RAb3OEq6uvHN-WMrW-sAnwbRqiXmdBpSPQDxbaAM M4T4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67130.RAb3OEq6uvHN-WMrW-sAnwbRqiXmdBpSPQDxbaAM M4T4130 assertion
type: Assertion
description: [NOD2 polymorphism screening should be used to optimize donor selection and antimicrobial prophylaxis to reduce the occurrence of aGVHD and TRM following allogeneic HSCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19219079
was generated by: ECO_0000203

NP67148.RAZwufTDadRzv3wTO4speTlIYbeEF3rBaYppe4rFu8wEA
has assertion: NP67148.RAZwufTDadRzv3wTO4speTlIYbeEF3rBaYppe4rFu8wEA130 assertion
has provenance: NP67148.RAZwufTDadRzv3wTO4speTlIYbeEF3rBaYppe4rFu8wEA130 provenance
has publication info: NP67148.RAZwufTDadRzv3wTO4speTlIYbeEF3rBaYppe4rFu8wEA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67148.RAZwufTDadRzv3wTO4speTlIYbeEF3rBaYppe4rFu8wEA130 assertion
type: Assertion
description: [These findings suggest that the association of PON1 Q192R with symptoms of depression in occupationally exposed groups may be driven by exposure to toxins that everyone in the general population is exposed to rather than exposure to toxins specifically used by sheep dippers or Gulf War veterans, or that other mechanisms underlie the 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/17183021
was generated by: ECO_0000203

NP67155.RAWfHZnbYk x1bxo 4aHgW66r636ZZ5jDbvTA-nu5W798
has assertion: NP67155.RAWfHZnbYk x1bxo 4aHgW66r636ZZ5jDbvTA-nu5W798130 assertion
has provenance: NP67155.RAWfHZnbYk x1bxo 4aHgW66r636ZZ5jDbvTA-nu5W798130 provenance
has publication info: NP67155.RAWfHZnbYk x1bxo 4aHgW66r636ZZ5jDbvTA-nu5W798130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67155.RAWfHZnbYk x1bxo 4aHgW66r636ZZ5jDbvTA-nu5W798130 assertion
type: Assertion
description: [A novel single nucleotide polymorphism, IVS2 -97A>T, in the prostaglandin F2alpha receptor gene was identified among the Malaysian patients with glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17582204
was generated by: ECO_0000203

NP67157.RAdgBzXS6aeHk VwjcYKbQLduNByiB1aEEmaMaDz1XKNc
has assertion: NP67157.RAdgBzXS6aeHk VwjcYKbQLduNByiB1aEEmaMaDz1XKNc130 assertion
has provenance: NP67157.RAdgBzXS6aeHk VwjcYKbQLduNByiB1aEEmaMaDz1XKNc130 provenance
has publication info: NP67157.RAdgBzXS6aeHk VwjcYKbQLduNByiB1aEEmaMaDz1XKNc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67157.RAdgBzXS6aeHk VwjcYKbQLduNByiB1aEEmaMaDz1XKNc130 assertion
type: Assertion
description: [The cyclooxygenase 2 -765 C promoter allele is a protective factor 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/16309832
was generated by: ECO_0000203

NP67164.RAZEtmRZMGHKFSuBiLKz4bhDRCCtlI-KgYruMaFz3OtUE
has assertion: NP67164.RAZEtmRZMGHKFSuBiLKz4bhDRCCtlI-KgYruMaFz3OtUE130 assertion
has provenance: NP67164.RAZEtmRZMGHKFSuBiLKz4bhDRCCtlI-KgYruMaFz3OtUE130 provenance
has publication info: NP67164.RAZEtmRZMGHKFSuBiLKz4bhDRCCtlI-KgYruMaFz3OtUE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67164.RAZEtmRZMGHKFSuBiLKz4bhDRCCtlI-KgYruMaFz3OtUE130 assertion
type: Assertion
description: [Antithrombin Cambridge II (A384S): an underestimated genetic risk factor for venous thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17244682
was generated by: ECO_0000203

NP67165.RAVblXouK2uXrbCqQ5 b3-VNh9UZTdq4Cx7dmrzquEM48
has assertion: NP67165.RAVblXouK2uXrbCqQ5 b3-VNh9UZTdq4Cx7dmrzquEM48130 assertion
has provenance: NP67165.RAVblXouK2uXrbCqQ5 b3-VNh9UZTdq4Cx7dmrzquEM48130 provenance
has publication info: NP67165.RAVblXouK2uXrbCqQ5 b3-VNh9UZTdq4Cx7dmrzquEM48130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67165.RAVblXouK2uXrbCqQ5 b3-VNh9UZTdq4Cx7dmrzquEM48130 assertion
type: Assertion
description: [Prevalence of SLC22A4 1672T and SLC22A5 -207C combination defined TC haplotype in Hungarian ulcerative colitis 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/17387389
was generated by: ECO_0000203

NP67167.RAUGx0jIYuy7STgJBWMuHV9-SERXIzilkIhpad3KAcByI
has assertion: NP67167.RAUGx0jIYuy7STgJBWMuHV9-SERXIzilkIhpad3KAcByI130 assertion
has provenance: NP67167.RAUGx0jIYuy7STgJBWMuHV9-SERXIzilkIhpad3KAcByI130 provenance
has publication info: NP67167.RAUGx0jIYuy7STgJBWMuHV9-SERXIzilkIhpad3KAcByI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67167.RAUGx0jIYuy7STgJBWMuHV9-SERXIzilkIhpad3KAcByI130 assertion
type: Assertion
description: [Prevalence of SLC22A4 1672T and SLC22A5 -207C combination defined TC haplotype in Hungarian ulcerative colitis 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/17387389
was generated by: ECO_0000203

NP67168.RAWrmf3w2NOv3DSFXx7zq3rdRE9hm7tYBnlJGlNbplwBE
has assertion: NP67168.RAWrmf3w2NOv3DSFXx7zq3rdRE9hm7tYBnlJGlNbplwBE130 assertion
has provenance: NP67168.RAWrmf3w2NOv3DSFXx7zq3rdRE9hm7tYBnlJGlNbplwBE130 provenance
has publication info: NP67168.RAWrmf3w2NOv3DSFXx7zq3rdRE9hm7tYBnlJGlNbplwBE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67168.RAWrmf3w2NOv3DSFXx7zq3rdRE9hm7tYBnlJGlNbplwBE130 assertion
type: Assertion
description: [Genetic variation in the sodium-dependent vitamin C transporters, SLC23A1, and SLC23A2 and risk for preterm delivery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16357110
was generated by: ECO_0000203

NP67174.RAbz1X7ARuWhqwstOFlZiu7dbs3KpVoampaSJEwHmEFwU
has assertion: NP67174.RAbz1X7ARuWhqwstOFlZiu7dbs3KpVoampaSJEwHmEFwU130 assertion
has provenance: NP67174.RAbz1X7ARuWhqwstOFlZiu7dbs3KpVoampaSJEwHmEFwU130 provenance
has publication info: NP67174.RAbz1X7ARuWhqwstOFlZiu7dbs3KpVoampaSJEwHmEFwU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67174.RAbz1X7ARuWhqwstOFlZiu7dbs3KpVoampaSJEwHmEFwU130 assertion
type: Assertion
description: [The present preliminary study investigated possible association of the temporal lobe epilepsy (TLE) with the polymorphisms in several 5HT-related genes, including serotonin transporter (5HTT), monoamine oxidase A (MAO-A) and serotonin receptors 5HT-1A, 5HT-1B and 5HT-2C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20435093
was generated by: ECO_0000203

NP67176.RAbEfcFcAJUlpokfFALtdz1pPL3-lpdlaUPVVk nngqVk
has assertion: NP67176.RAbEfcFcAJUlpokfFALtdz1pPL3-lpdlaUPVVk nngqVk130 assertion
has provenance: NP67176.RAbEfcFcAJUlpokfFALtdz1pPL3-lpdlaUPVVk nngqVk130 provenance
has publication info: NP67176.RAbEfcFcAJUlpokfFALtdz1pPL3-lpdlaUPVVk nngqVk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67176.RAbEfcFcAJUlpokfFALtdz1pPL3-lpdlaUPVVk nngqVk130 assertion
type: Assertion
description: [There was no association between five single nucleotide polymorphisms or haplotypes of the OPN gene and aortic diameter or AAA expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17170369
was generated by: ECO_0000203

NP67178.RAaGz2pM9S8xlUXgh00XtK274rMwNiz0ymlVSOWzD4EdA
has assertion: NP67178.RAaGz2pM9S8xlUXgh00XtK274rMwNiz0ymlVSOWzD4EdA130 assertion
has provenance: NP67178.RAaGz2pM9S8xlUXgh00XtK274rMwNiz0ymlVSOWzD4EdA130 provenance
has publication info: NP67178.RAaGz2pM9S8xlUXgh00XtK274rMwNiz0ymlVSOWzD4EdA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67178.RAaGz2pM9S8xlUXgh00XtK274rMwNiz0ymlVSOWzD4EdA130 assertion
type: Assertion
description: [Association analysis of glycine- and serine-related genes in a Japanese population of patients 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/19223009
was generated by: ECO_0000203

NP67179.RATa5QZFtvCPxs RzTJ2EqvKF4kXY4iGu72vlfDKFjIE0
has assertion: NP67179.RATa5QZFtvCPxs RzTJ2EqvKF4kXY4iGu72vlfDKFjIE0130 assertion
has provenance: NP67179.RATa5QZFtvCPxs RzTJ2EqvKF4kXY4iGu72vlfDKFjIE0130 provenance
has publication info: NP67179.RATa5QZFtvCPxs RzTJ2EqvKF4kXY4iGu72vlfDKFjIE0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67179.RATa5QZFtvCPxs RzTJ2EqvKF4kXY4iGu72vlfDKFjIE0130 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

NP67180.RAVfuMPN3cL 2LcfNoX29aR81lB8B1UbOF6PZztjrOQ7Q
has assertion: NP67180.RAVfuMPN3cL 2LcfNoX29aR81lB8B1UbOF6PZztjrOQ7Q130 assertion
has provenance: NP67180.RAVfuMPN3cL 2LcfNoX29aR81lB8B1UbOF6PZztjrOQ7Q130 provenance
has publication info: NP67180.RAVfuMPN3cL 2LcfNoX29aR81lB8B1UbOF6PZztjrOQ7Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67180.RAVfuMPN3cL 2LcfNoX29aR81lB8B1UbOF6PZztjrOQ7Q130 assertion
type: Assertion
description: [A case-control study investigating the role of sulfotransferase 1A1 polymorphism in head and neck 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/16575574
was generated by: ECO_0000203

NP67181.RAdtZpiKB3QwHKllVHwkGIMGlGy4IXz2tH6hgfDF7JAhA
has assertion: NP67181.RAdtZpiKB3QwHKllVHwkGIMGlGy4IXz2tH6hgfDF7JAhA130 assertion
has provenance: NP67181.RAdtZpiKB3QwHKllVHwkGIMGlGy4IXz2tH6hgfDF7JAhA130 provenance
has publication info: NP67181.RAdtZpiKB3QwHKllVHwkGIMGlGy4IXz2tH6hgfDF7JAhA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67181.RAdtZpiKB3QwHKllVHwkGIMGlGy4IXz2tH6hgfDF7JAhA130 assertion
type: Assertion
description: [Our findings have suggested that there was a significant association between brain tumor and SULT1A1*2 allele (A allele that is also known as His allele) and this allele is an important risk factor in the development of meningiomal brain tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17605044
was generated by: ECO_0000203

NP67183.RAWegCn3r8sInpsW36qqgBCva0t3exEZL7dLUyImzn36Y
has assertion: NP67183.RAWegCn3r8sInpsW36qqgBCva0t3exEZL7dLUyImzn36Y130 assertion
has provenance: NP67183.RAWegCn3r8sInpsW36qqgBCva0t3exEZL7dLUyImzn36Y130 provenance
has publication info: NP67183.RAWegCn3r8sInpsW36qqgBCva0t3exEZL7dLUyImzn36Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67183.RAWegCn3r8sInpsW36qqgBCva0t3exEZL7dLUyImzn36Y130 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

NP67190.RATRi9mU0xxSJXpqVuMy6AgL4ovtdmPLEazpwRyWn0l c
has assertion: NP67190.RATRi9mU0xxSJXpqVuMy6AgL4ovtdmPLEazpwRyWn0l c130 assertion
has provenance: NP67190.RATRi9mU0xxSJXpqVuMy6AgL4ovtdmPLEazpwRyWn0l c130 provenance
has publication info: NP67190.RATRi9mU0xxSJXpqVuMy6AgL4ovtdmPLEazpwRyWn0l c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67190.RATRi9mU0xxSJXpqVuMy6AgL4ovtdmPLEazpwRyWn0l c130 assertion
type: Assertion
description: [Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17130424
was generated by: ECO_0000203

NP67193.RAT VE1uf-n4UoIfCzLAEhezRtI4iSZyIA73JQuY7TI0I
has assertion: NP67193.RAT VE1uf-n4UoIfCzLAEhezRtI4iSZyIA73JQuY7TI0I130 assertion
has provenance: NP67193.RAT VE1uf-n4UoIfCzLAEhezRtI4iSZyIA73JQuY7TI0I130 provenance
has publication info: NP67193.RAT VE1uf-n4UoIfCzLAEhezRtI4iSZyIA73JQuY7TI0I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67193.RAT VE1uf-n4UoIfCzLAEhezRtI4iSZyIA73JQuY7TI0I130 assertion
type: Assertion
description: [Genetic variants in XRCC2: new insights into colorectal cancer tumorigenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19690184
was generated by: ECO_0000203

NP67194.RAbUrC7DC8K6HNmjSDP1IeTm5zCquo7qKAl-42D3YD27g
has assertion: NP67194.RAbUrC7DC8K6HNmjSDP1IeTm5zCquo7qKAl-42D3YD27g130 assertion
has provenance: NP67194.RAbUrC7DC8K6HNmjSDP1IeTm5zCquo7qKAl-42D3YD27g130 provenance
has publication info: NP67194.RAbUrC7DC8K6HNmjSDP1IeTm5zCquo7qKAl-42D3YD27g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67194.RAbUrC7DC8K6HNmjSDP1IeTm5zCquo7qKAl-42D3YD27g130 assertion
type: Assertion
description: [Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset 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/17373700
was generated by: ECO_0000203

NP67196.RAcaGYgaiFx4zB0zpdeFwzxffZhvsz0UatWFfbn5nJtNo
has assertion: NP67196.RAcaGYgaiFx4zB0zpdeFwzxffZhvsz0UatWFfbn5nJtNo130 assertion
has provenance: NP67196.RAcaGYgaiFx4zB0zpdeFwzxffZhvsz0UatWFfbn5nJtNo130 provenance
has publication info: NP67196.RAcaGYgaiFx4zB0zpdeFwzxffZhvsz0UatWFfbn5nJtNo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67196.RAcaGYgaiFx4zB0zpdeFwzxffZhvsz0UatWFfbn5nJtNo130 assertion
type: Assertion
description: [Common single nucleotide polymorphisms in Japanese patients with essential hypertension: aldehyde dehydrogenase 2 gene as a risk factor independent of alcohol consumption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17785925
was generated by: ECO_0000203

NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o
has assertion: NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130 assertion
has provenance: NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130 provenance
has publication info: NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130 assertion
type: Assertion
description: [This investigation indicates that DARC is not a genetic trait significantly associated with or predisposing to Behcet's disease, at least in Caucasian Italians. However, the role of this polymorphism in the development and in the clinical course of the disease awaits further 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/12739041
was generated by: ECO_0000203

NP67203.RAXkYy8Huib95qPxCr7nFyVItubW85bdFTMn85zfwdIdQ
has assertion: NP67203.RAXkYy8Huib95qPxCr7nFyVItubW85bdFTMn85zfwdIdQ130 assertion
has provenance: NP67203.RAXkYy8Huib95qPxCr7nFyVItubW85bdFTMn85zfwdIdQ130 provenance
has publication info: NP67203.RAXkYy8Huib95qPxCr7nFyVItubW85bdFTMn85zfwdIdQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67203.RAXkYy8Huib95qPxCr7nFyVItubW85bdFTMn85zfwdIdQ130 assertion
type: Assertion
description: [Association between sodium- and potassium-activated adenosine triphosphatase alpha isoforms and bipolar 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/19058785
was generated by: ECO_0000203

NP67205.RAWBCpGRibbou3bzm1NQSnKpBuSi6gHgScaN9txeP CMI
has assertion: NP67205.RAWBCpGRibbou3bzm1NQSnKpBuSi6gHgScaN9txeP CMI130 assertion
has provenance: NP67205.RAWBCpGRibbou3bzm1NQSnKpBuSi6gHgScaN9txeP CMI130 provenance
has publication info: NP67205.RAWBCpGRibbou3bzm1NQSnKpBuSi6gHgScaN9txeP CMI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67205.RAWBCpGRibbou3bzm1NQSnKpBuSi6gHgScaN9txeP CMI130 assertion
type: Assertion
description: [Association between deletion polymorphism of the angiotensin-converting enzyme gene and cerebral 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/8704045
was generated by: ECO_0000203

NP67206.RAbb6L0nfO10TQM89JLVjhOcCu7EFnTHWkzUXGl-5O13g
has assertion: NP67206.RAbb6L0nfO10TQM89JLVjhOcCu7EFnTHWkzUXGl-5O13g130 assertion
has provenance: NP67206.RAbb6L0nfO10TQM89JLVjhOcCu7EFnTHWkzUXGl-5O13g130 provenance
has publication info: NP67206.RAbb6L0nfO10TQM89JLVjhOcCu7EFnTHWkzUXGl-5O13g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67206.RAbb6L0nfO10TQM89JLVjhOcCu7EFnTHWkzUXGl-5O13g130 assertion
type: Assertion
description: [Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin 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/16059747
was generated by: ECO_0000203

NP67208.RARUC-S8XITT2PPfjS6zHn3BIQhiJWfb5NsTiZaLMNx9k
has assertion: NP67208.RARUC-S8XITT2PPfjS6zHn3BIQhiJWfb5NsTiZaLMNx9k130 assertion
has provenance: NP67208.RARUC-S8XITT2PPfjS6zHn3BIQhiJWfb5NsTiZaLMNx9k130 provenance
has publication info: NP67208.RARUC-S8XITT2PPfjS6zHn3BIQhiJWfb5NsTiZaLMNx9k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67208.RARUC-S8XITT2PPfjS6zHn3BIQhiJWfb5NsTiZaLMNx9k130 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

NP67209.RASVrBtIyLzU1WMKZiYAKgXPZEyp8fY7i881xL-JsK3 s
has assertion: NP67209.RASVrBtIyLzU1WMKZiYAKgXPZEyp8fY7i881xL-JsK3 s130 assertion
has provenance: NP67209.RASVrBtIyLzU1WMKZiYAKgXPZEyp8fY7i881xL-JsK3 s130 provenance
has publication info: NP67209.RASVrBtIyLzU1WMKZiYAKgXPZEyp8fY7i881xL-JsK3 s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67209.RASVrBtIyLzU1WMKZiYAKgXPZEyp8fY7i881xL-JsK3 s130 assertion
type: Assertion
description: [On the basis of our findings and earlier reports, MYH mutation screening should be considered if all of the following criteria are fulfilled: (i) presence of classical or attenuated polyposis coli, (ii) absence of a pathogenic APC mutation, and (iii) a family history compatible with an autosomal recessive mode of inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16287072
was generated by: ECO_0000203

NP67213.RAQG83wCwQT7kUcLDE0jU4fnhBMCvD5s2M55qiQGdHf8E
has assertion: NP67213.RAQG83wCwQT7kUcLDE0jU4fnhBMCvD5s2M55qiQGdHf8E130 assertion
has provenance: NP67213.RAQG83wCwQT7kUcLDE0jU4fnhBMCvD5s2M55qiQGdHf8E130 provenance
has publication info: NP67213.RAQG83wCwQT7kUcLDE0jU4fnhBMCvD5s2M55qiQGdHf8E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67213.RAQG83wCwQT7kUcLDE0jU4fnhBMCvD5s2M55qiQGdHf8E130 assertion
type: Assertion
description: [These findings suggest that breast cancer phenotype and outcome can be influenced by common functional polymorphisms in MMP 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/15609121
was generated by: ECO_0000203

NP67214.RASoPC4fr42In CoXOTIBtdGh9ZPVPHiCV6BftGIjorHU
has assertion: NP67214.RASoPC4fr42In CoXOTIBtdGh9ZPVPHiCV6BftGIjorHU130 assertion
has provenance: NP67214.RASoPC4fr42In CoXOTIBtdGh9ZPVPHiCV6BftGIjorHU130 provenance
has publication info: NP67214.RASoPC4fr42In CoXOTIBtdGh9ZPVPHiCV6BftGIjorHU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67214.RASoPC4fr42In CoXOTIBtdGh9ZPVPHiCV6BftGIjorHU130 assertion
type: Assertion
description: [Promoter polymorphisms in matrix metalloproteinases and their inhibitors: few associations with breast cancer susceptibility 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/17033924
was generated by: ECO_0000203

NP67216.RASIH-vyH3er4YbrlEflUsQWCOii3RBfm3fKhW mKFCcs
has assertion: NP67216.RASIH-vyH3er4YbrlEflUsQWCOii3RBfm3fKhW mKFCcs130 assertion
has provenance: NP67216.RASIH-vyH3er4YbrlEflUsQWCOii3RBfm3fKhW mKFCcs130 provenance
has publication info: NP67216.RASIH-vyH3er4YbrlEflUsQWCOii3RBfm3fKhW mKFCcs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67216.RASIH-vyH3er4YbrlEflUsQWCOii3RBfm3fKhW mKFCcs130 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

NP67220.RAcwIxJdUEHtzPOp-ov2zv6M3Xp17e59Tz-RTgzKyvSb8
has assertion: NP67220.RAcwIxJdUEHtzPOp-ov2zv6M3Xp17e59Tz-RTgzKyvSb8130 assertion
has provenance: NP67220.RAcwIxJdUEHtzPOp-ov2zv6M3Xp17e59Tz-RTgzKyvSb8130 provenance
has publication info: NP67220.RAcwIxJdUEHtzPOp-ov2zv6M3Xp17e59Tz-RTgzKyvSb8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67220.RAcwIxJdUEHtzPOp-ov2zv6M3Xp17e59Tz-RTgzKyvSb8130 assertion
type: Assertion
description: [A new platelet polymorphism Duv(a+), localized within the RGD binding domain of glycoprotein IIIa, is associated with neonatal thrombocytopenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12036875
was generated by: ECO_0000203

NP67222.RAT1FdHfXTNn6faiYJfu9u16yyCm kx1J9xDgh084TxCI
has assertion: NP67222.RAT1FdHfXTNn6faiYJfu9u16yyCm kx1J9xDgh084TxCI130 assertion
has provenance: NP67222.RAT1FdHfXTNn6faiYJfu9u16yyCm kx1J9xDgh084TxCI130 provenance
has publication info: NP67222.RAT1FdHfXTNn6faiYJfu9u16yyCm kx1J9xDgh084TxCI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67222.RAT1FdHfXTNn6faiYJfu9u16yyCm kx1J9xDgh084TxCI130 assertion
type: Assertion
description: [A recurrent large Alu-mediated deletion in the hypoxanthine phosphoribosyltransferase (HPRT1) gene associated with Lesch-Nyhan 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/11668636
was generated by: ECO_0000203

NP67226.RAdcHtLGRrosXuRlgQe-QSdHP2QcJMYunlPiabH06pohA
has assertion: NP67226.RAdcHtLGRrosXuRlgQe-QSdHP2QcJMYunlPiabH06pohA130 assertion
has provenance: NP67226.RAdcHtLGRrosXuRlgQe-QSdHP2QcJMYunlPiabH06pohA130 provenance
has publication info: NP67226.RAdcHtLGRrosXuRlgQe-QSdHP2QcJMYunlPiabH06pohA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67226.RAdcHtLGRrosXuRlgQe-QSdHP2QcJMYunlPiabH06pohA130 assertion
type: Assertion
description: [This deletion reduces TNP1 expression and may cause human male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16291974
was generated by: ECO_0000203

NP67227.RASJz6EotWghhsEMU45hjo99O1k6 HoV7TRR0xU12rzNI
has assertion: NP67227.RASJz6EotWghhsEMU45hjo99O1k6 HoV7TRR0xU12rzNI130 assertion
has provenance: NP67227.RASJz6EotWghhsEMU45hjo99O1k6 HoV7TRR0xU12rzNI130 provenance
has publication info: NP67227.RASJz6EotWghhsEMU45hjo99O1k6 HoV7TRR0xU12rzNI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67227.RASJz6EotWghhsEMU45hjo99O1k6 HoV7TRR0xU12rzNI130 assertion
type: Assertion
description: [The His645Asp polymorphism of the histamine metabolising enzyme ABP1 is related to severity of ulcerative colitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16489678
was generated by: ECO_0000203

NP67228.RAfoI4JM4VtMDUakKV6-BMLsSm3hid6cUg g3NI9-2xDQ
has assertion: NP67228.RAfoI4JM4VtMDUakKV6-BMLsSm3hid6cUg g3NI9-2xDQ130 assertion
has provenance: NP67228.RAfoI4JM4VtMDUakKV6-BMLsSm3hid6cUg g3NI9-2xDQ130 provenance
has publication info: NP67228.RAfoI4JM4VtMDUakKV6-BMLsSm3hid6cUg g3NI9-2xDQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67228.RAfoI4JM4VtMDUakKV6-BMLsSm3hid6cUg g3NI9-2xDQ130 assertion
type: Assertion
description: [ACE gene deletion polymorphism may be operative in response to medical treatment that included ACE inhibitors in patients with HF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18516385
was generated by: ECO_0000203

NP67229.RAfnsom7tSj025NEBzjTJVtGriHFKe2ES-XmxY52PYFvg
has assertion: NP67229.RAfnsom7tSj025NEBzjTJVtGriHFKe2ES-XmxY52PYFvg130 assertion
has provenance: NP67229.RAfnsom7tSj025NEBzjTJVtGriHFKe2ES-XmxY52PYFvg130 provenance
has publication info: NP67229.RAfnsom7tSj025NEBzjTJVtGriHFKe2ES-XmxY52PYFvg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67229.RAfnsom7tSj025NEBzjTJVtGriHFKe2ES-XmxY52PYFvg130 assertion
type: Assertion
description: [: This study suggests that ACE I/D polymorphism might represent a predisposing factor to severe heart failure, independently of well-known prognostic markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19050458
was generated by: ECO_0000203

NP67231.RAZAHeP7TlN R99ybYKHeTh2Z52avilEZPIDq6RKnJY0M
has assertion: NP67231.RAZAHeP7TlN R99ybYKHeTh2Z52avilEZPIDq6RKnJY0M130 assertion
has provenance: NP67231.RAZAHeP7TlN R99ybYKHeTh2Z52avilEZPIDq6RKnJY0M130 provenance
has publication info: NP67231.RAZAHeP7TlN R99ybYKHeTh2Z52avilEZPIDq6RKnJY0M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67231.RAZAHeP7TlN R99ybYKHeTh2Z52avilEZPIDq6RKnJY0M130 assertion
type: Assertion
description: [Effect of the polymorphism of the angiotensin-converting enzyme gene on the plasma angiotensin II levels and the risk of 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/16145913
was generated by: ECO_0000203

NP67235.RAYDzVK1O9dSPWXH9NU7xAoWk0n8ab4fnibr4wXk3zVIY
has assertion: NP67235.RAYDzVK1O9dSPWXH9NU7xAoWk0n8ab4fnibr4wXk3zVIY130 assertion
has provenance: NP67235.RAYDzVK1O9dSPWXH9NU7xAoWk0n8ab4fnibr4wXk3zVIY130 provenance
has publication info: NP67235.RAYDzVK1O9dSPWXH9NU7xAoWk0n8ab4fnibr4wXk3zVIY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67235.RAYDzVK1O9dSPWXH9NU7xAoWk0n8ab4fnibr4wXk3zVIY130 assertion
type: Assertion
description: [Angiotensin-converting-enzyme gene polymorphism and heart failure: 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/14602526
was generated by: ECO_0000203

NP67241.RAQfEqFcQcynoH2ht1ZE8X5tciX-Hm11ukOdpKPcof3cc
has assertion: NP67241.RAQfEqFcQcynoH2ht1ZE8X5tciX-Hm11ukOdpKPcof3cc130 assertion
has provenance: NP67241.RAQfEqFcQcynoH2ht1ZE8X5tciX-Hm11ukOdpKPcof3cc130 provenance
has publication info: NP67241.RAQfEqFcQcynoH2ht1ZE8X5tciX-Hm11ukOdpKPcof3cc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67241.RAQfEqFcQcynoH2ht1ZE8X5tciX-Hm11ukOdpKPcof3cc130 assertion
type: Assertion
description: [Angiotensin II type 2 receptor gene polymorphism in Caucasian children with a wide spectrum of congenital anomalies of the kidney and urinary tract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17515833
was generated by: ECO_0000203

NP67242.RARCPBbvFF5E5ssSe-o64OXPxGu9cgBSKG09i36dMs7So
has assertion: NP67242.RARCPBbvFF5E5ssSe-o64OXPxGu9cgBSKG09i36dMs7So130 assertion
has provenance: NP67242.RARCPBbvFF5E5ssSe-o64OXPxGu9cgBSKG09i36dMs7So130 provenance
has publication info: NP67242.RARCPBbvFF5E5ssSe-o64OXPxGu9cgBSKG09i36dMs7So130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67242.RARCPBbvFF5E5ssSe-o64OXPxGu9cgBSKG09i36dMs7So130 assertion
type: Assertion
description: [Angiotensin II type 2 receptor gene polymorphism in Caucasian children with a wide spectrum of congenital anomalies of the kidney and urinary tract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17515833
was generated by: ECO_0000203

NP67243.RAQmLcAf1bFaRm3EC Ty1xBmBtU1ed1xtr-YGEVqyPjxs
has assertion: NP67243.RAQmLcAf1bFaRm3EC Ty1xBmBtU1ed1xtr-YGEVqyPjxs130 assertion
has provenance: NP67243.RAQmLcAf1bFaRm3EC Ty1xBmBtU1ed1xtr-YGEVqyPjxs130 provenance
has publication info: NP67243.RAQmLcAf1bFaRm3EC Ty1xBmBtU1ed1xtr-YGEVqyPjxs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67243.RAQmLcAf1bFaRm3EC Ty1xBmBtU1ed1xtr-YGEVqyPjxs130 assertion
type: Assertion
description: [Mutations in AGXT, a locus mapped to 2q37.3, cause deficiency of liver-specific alanine:glyoxylate aminotransferase (AGT), the metabolic error in type 1 primary hyperoxaluria (PH1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17460142
was generated by: ECO_0000203

NP67246.RAVUbP4Sq2PPhYFacyOwdGJ1900O9j2N3Vqtpr3BBBQpg
has assertion: NP67246.RAVUbP4Sq2PPhYFacyOwdGJ1900O9j2N3Vqtpr3BBBQpg130 assertion
has provenance: NP67246.RAVUbP4Sq2PPhYFacyOwdGJ1900O9j2N3Vqtpr3BBBQpg130 provenance
has publication info: NP67246.RAVUbP4Sq2PPhYFacyOwdGJ1900O9j2N3Vqtpr3BBBQpg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67246.RAVUbP4Sq2PPhYFacyOwdGJ1900O9j2N3Vqtpr3BBBQpg130 assertion
type: Assertion
description: [TagSNP evaluation for the association of 42 inflammation loci and vascular disease: evidence of IL6, FGB, ALOX5, NFKBIA, and IL4R loci effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17115186
was generated by: ECO_0000203

NP67248.RAdyHmdLgFiCTeHZkiBjr 13ZthBW9nFxPBVDtL41ZVOk
has assertion: NP67248.RAdyHmdLgFiCTeHZkiBjr 13ZthBW9nFxPBVDtL41ZVOk130 assertion
has provenance: NP67248.RAdyHmdLgFiCTeHZkiBjr 13ZthBW9nFxPBVDtL41ZVOk130 provenance
has publication info: NP67248.RAdyHmdLgFiCTeHZkiBjr 13ZthBW9nFxPBVDtL41ZVOk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67248.RAdyHmdLgFiCTeHZkiBjr 13ZthBW9nFxPBVDtL41ZVOk130 assertion
type: Assertion
description: [Genotype at the Asp148Glu SNP site in the APEX gene of the base excision repair (BER) pathway was associated with childhood cancer in survivors (P = 0.001, significant even after multiple test adjustment), due to the enhanced frequency of the APEX Asp148 allele among survivors in comparison to that of their partners.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17177211
was generated by: ECO_0000203

NP67249.RAXfVjUWNSCVgYBttnyPSBle9jWVqfttlVzs8ui7SBpxk
has assertion: NP67249.RAXfVjUWNSCVgYBttnyPSBle9jWVqfttlVzs8ui7SBpxk130 assertion
has provenance: NP67249.RAXfVjUWNSCVgYBttnyPSBle9jWVqfttlVzs8ui7SBpxk130 provenance
has publication info: NP67249.RAXfVjUWNSCVgYBttnyPSBle9jWVqfttlVzs8ui7SBpxk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67249.RAXfVjUWNSCVgYBttnyPSBle9jWVqfttlVzs8ui7SBpxk130 assertion
type: Assertion
description: [For the prediction of ONFH, it is useful to analyze ApoB C7623T and plasma ApoB/ApoA1 ratio before the administration of steroids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17530370
was generated by: ECO_0000203

NP67253.RAV3fx-4iNJdfzHcGRQBc6s3GGAqmEMsf3naaWCP7C-sA
has assertion: NP67253.RAV3fx-4iNJdfzHcGRQBc6s3GGAqmEMsf3naaWCP7C-sA130 assertion
has provenance: NP67253.RAV3fx-4iNJdfzHcGRQBc6s3GGAqmEMsf3naaWCP7C-sA130 provenance
has publication info: NP67253.RAV3fx-4iNJdfzHcGRQBc6s3GGAqmEMsf3naaWCP7C-sA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67253.RAV3fx-4iNJdfzHcGRQBc6s3GGAqmEMsf3naaWCP7C-sA130 assertion
type: Assertion
description: [Differential association of circadian genes with mood disorders: CRY1 and NPAS2 are associated with unipolar major depression and CLOCK and VIP with 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/20072116
was generated by: ECO_0000203

NP67256.RAaAmrFc4i24HLaUvevWkHlnz8gKhQ 3bGl4T0U fo34U
has assertion: NP67256.RAaAmrFc4i24HLaUvevWkHlnz8gKhQ 3bGl4T0U fo34U130 assertion
has provenance: NP67256.RAaAmrFc4i24HLaUvevWkHlnz8gKhQ 3bGl4T0U fo34U130 provenance
has publication info: NP67256.RAaAmrFc4i24HLaUvevWkHlnz8gKhQ 3bGl4T0U fo34U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67256.RAaAmrFc4i24HLaUvevWkHlnz8gKhQ 3bGl4T0U fo34U130 assertion
type: Assertion
description: [Single nucleotide polymorphisms of RecQ1, RAD54L, and ATM genes are associated with reduced survival 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/16520463
was generated by: ECO_0000203

NP67258.RAVJiJzqtmcCiavr3YS6NLnQ3vSWe s3ba6P177repjKw
has assertion: NP67258.RAVJiJzqtmcCiavr3YS6NLnQ3vSWe s3ba6P177repjKw130 assertion
has provenance: NP67258.RAVJiJzqtmcCiavr3YS6NLnQ3vSWe s3ba6P177repjKw130 provenance
has publication info: NP67258.RAVJiJzqtmcCiavr3YS6NLnQ3vSWe s3ba6P177repjKw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67258.RAVJiJzqtmcCiavr3YS6NLnQ3vSWe s3ba6P177repjKw130 assertion
type: Assertion
description: [Germline BCL-2 sequence variants and inherited predisposition to 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/16733517
was generated by: ECO_0000203

NP67259.RAXkUXFRqdllBN5qIWgeOndAXr8A5hpS2jA1ZdhAEkqwM
has assertion: NP67259.RAXkUXFRqdllBN5qIWgeOndAXr8A5hpS2jA1ZdhAEkqwM130 assertion
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has publication info: NP67259.RAXkUXFRqdllBN5qIWgeOndAXr8A5hpS2jA1ZdhAEkqwM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67259.RAXkUXFRqdllBN5qIWgeOndAXr8A5hpS2jA1ZdhAEkqwM130 assertion
type: Assertion
description: [Polymorphisms in mitochondrial genes 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/19064571
was generated by: ECO_0000203

NP67260.RAZIO4oTvRv3pLk-i88wb1MJz0j0DHjBjMFw3godq16Wk
has assertion: NP67260.RAZIO4oTvRv3pLk-i88wb1MJz0j0DHjBjMFw3godq16Wk130 assertion
has provenance: NP67260.RAZIO4oTvRv3pLk-i88wb1MJz0j0DHjBjMFw3godq16Wk130 provenance
has publication info: NP67260.RAZIO4oTvRv3pLk-i88wb1MJz0j0DHjBjMFw3godq16Wk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67260.RAZIO4oTvRv3pLk-i88wb1MJz0j0DHjBjMFw3godq16Wk130 assertion
type: Assertion
description: [Brain-derived neurotrophic factor gene polymorphism (Val66Met) and citalopram response in 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/16979146
was generated by: ECO_0000203

NP67262.RAfFfe2KtS9xAupFDB VW5TE80Q6CcIncLd Q6jTClDwM
has assertion: NP67262.RAfFfe2KtS9xAupFDB VW5TE80Q6CcIncLd Q6jTClDwM130 assertion
has provenance: NP67262.RAfFfe2KtS9xAupFDB VW5TE80Q6CcIncLd Q6jTClDwM130 provenance
has publication info: NP67262.RAfFfe2KtS9xAupFDB VW5TE80Q6CcIncLd Q6jTClDwM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67262.RAfFfe2KtS9xAupFDB VW5TE80Q6CcIncLd Q6jTClDwM130 assertion
type: Assertion
description: [Review and meta-analysis of antidepressant pharmacogenetic findings in 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/18982004
was generated by: ECO_0000203

NP67263.RASWWHtasSPH9zCRAu2nbL-rPUiOEEbtMAWYH Grlrfow
has assertion: NP67263.RASWWHtasSPH9zCRAu2nbL-rPUiOEEbtMAWYH Grlrfow130 assertion
has provenance: NP67263.RASWWHtasSPH9zCRAu2nbL-rPUiOEEbtMAWYH Grlrfow130 provenance
has publication info: NP67263.RASWWHtasSPH9zCRAu2nbL-rPUiOEEbtMAWYH Grlrfow130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67263.RASWWHtasSPH9zCRAu2nbL-rPUiOEEbtMAWYH Grlrfow130 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

NP67270.RAbfRKmx5eUbhn3B EX1aMAYNLHMOeBEav2O0q4EXYKek
has assertion: NP67270.RAbfRKmx5eUbhn3B EX1aMAYNLHMOeBEav2O0q4EXYKek130 assertion
has provenance: NP67270.RAbfRKmx5eUbhn3B EX1aMAYNLHMOeBEav2O0q4EXYKek130 provenance
has publication info: NP67270.RAbfRKmx5eUbhn3B EX1aMAYNLHMOeBEav2O0q4EXYKek130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67270.RAbfRKmx5eUbhn3B EX1aMAYNLHMOeBEav2O0q4EXYKek130 assertion
type: Assertion
description: [Analogously, results from DBMA found a five-locus combination, two in ST6GALNAC2 and three in C1GALT1, which was associated with IgAN predisposition, eGFR, and renal outcome of patients with IgAN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19357720
was generated by: ECO_0000203

NP67279.RAcXJrcvbRo iytwNsuZTcF2yxlYz4PJRXv6aiNQXbcUY
has assertion: NP67279.RAcXJrcvbRo iytwNsuZTcF2yxlYz4PJRXv6aiNQXbcUY130 assertion
has provenance: NP67279.RAcXJrcvbRo iytwNsuZTcF2yxlYz4PJRXv6aiNQXbcUY130 provenance
has publication info: NP67279.RAcXJrcvbRo iytwNsuZTcF2yxlYz4PJRXv6aiNQXbcUY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67279.RAcXJrcvbRo iytwNsuZTcF2yxlYz4PJRXv6aiNQXbcUY130 assertion
type: Assertion
description: [A polymorphism in the promoter region of the CD86 (B7.2) gene is associated with systemic 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/16712644
was generated by: ECO_0000203

NP67284.RASHzNqEiiR0QgKGniljWjnXjuR4vaPWqtFljNsVbwIy8
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has publication info: NP67284.RASHzNqEiiR0QgKGniljWjnXjuR4vaPWqtFljNsVbwIy8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67284.RASHzNqEiiR0QgKGniljWjnXjuR4vaPWqtFljNsVbwIy8130 assertion
type: Assertion
description: [Comprehensive assessment of P21 polymorphisms and lung 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/18046503
was generated by: ECO_0000203

NP67287.RAYAU MW RYZuWqJ9d51O86PcmGVwMMA7OXjNLknTm2J4
has assertion: NP67287.RAYAU MW RYZuWqJ9d51O86PcmGVwMMA7OXjNLknTm2J4130 assertion
has provenance: NP67287.RAYAU MW RYZuWqJ9d51O86PcmGVwMMA7OXjNLknTm2J4130 provenance
has publication info: NP67287.RAYAU MW RYZuWqJ9d51O86PcmGVwMMA7OXjNLknTm2J4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67287.RAYAU MW RYZuWqJ9d51O86PcmGVwMMA7OXjNLknTm2J4130 assertion
type: Assertion
description: [Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared 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/17554300
was generated by: ECO_0000203

NP67298.RAa4LG0E79fMnm6J6xzr7HiCwpD2ZfFhIHgQ-9n2OnRdY
has assertion: NP67298.RAa4LG0E79fMnm6J6xzr7HiCwpD2ZfFhIHgQ-9n2OnRdY130 assertion
has provenance: NP67298.RAa4LG0E79fMnm6J6xzr7HiCwpD2ZfFhIHgQ-9n2OnRdY130 provenance
has publication info: NP67298.RAa4LG0E79fMnm6J6xzr7HiCwpD2ZfFhIHgQ-9n2OnRdY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67298.RAa4LG0E79fMnm6J6xzr7HiCwpD2ZfFhIHgQ-9n2OnRdY130 assertion
type: Assertion
description: [CTLA-4 gene polymorphisms and natural soluble CTLA-4 protein in 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/16712655
was generated by: ECO_0000203

NP67300.RAecZhuAsrG4 W pUaGYhUNxeJ5kpRrcZfLEi2zYWlkJo
has assertion: NP67300.RAecZhuAsrG4 W pUaGYhUNxeJ5kpRrcZfLEi2zYWlkJo130 assertion
has provenance: NP67300.RAecZhuAsrG4 W pUaGYhUNxeJ5kpRrcZfLEi2zYWlkJo130 provenance
has publication info: NP67300.RAecZhuAsrG4 W pUaGYhUNxeJ5kpRrcZfLEi2zYWlkJo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67300.RAecZhuAsrG4 W pUaGYhUNxeJ5kpRrcZfLEi2zYWlkJo130 assertion
type: Assertion
description: [IL-6 174 G/C, FVL, and Cathepsin G (Ars 125 Ser) did not influence the incidence and mortality 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/16444434
was generated by: ECO_0000203

NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4
has assertion: NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130 assertion
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has publication info: NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67304.RAUylPtCI0245MeYG4M9JBgX2FvrTccpteZv3l53HrbZ4130 assertion
type: Assertion
description: [indicate that common alleles of the CYP11alpha promoter pentannucleotide (tttta)n polymorphism in this population of Han Chinese women were P4, P6 and P8, and allele P6 was the most common one.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19300392
was generated by: ECO_0000203

NP67314.RAU47z8dLPL8n79kLb7vuLhMANQRfmzPINhE0WvpQvm4M
has assertion: NP67314.RAU47z8dLPL8n79kLb7vuLhMANQRfmzPINhE0WvpQvm4M130 assertion
has provenance: NP67314.RAU47z8dLPL8n79kLb7vuLhMANQRfmzPINhE0WvpQvm4M130 provenance
has publication info: NP67314.RAU47z8dLPL8n79kLb7vuLhMANQRfmzPINhE0WvpQvm4M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67314.RAU47z8dLPL8n79kLb7vuLhMANQRfmzPINhE0WvpQvm4M130 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

NP67315.RAXVbEO0a i-0zpcXEnkofBAuf- VI6VNiK-ebqBQv0Aw
has assertion: NP67315.RAXVbEO0a i-0zpcXEnkofBAuf- VI6VNiK-ebqBQv0Aw130 assertion
has provenance: NP67315.RAXVbEO0a i-0zpcXEnkofBAuf- VI6VNiK-ebqBQv0Aw130 provenance
has publication info: NP67315.RAXVbEO0a i-0zpcXEnkofBAuf- VI6VNiK-ebqBQv0Aw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67315.RAXVbEO0a i-0zpcXEnkofBAuf- VI6VNiK-ebqBQv0Aw130 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

NP67317.RAQLU Wm3-TxodHQXJeBa cQGYsa9Rx8n2JOscJxiN9I4
has assertion: NP67317.RAQLU Wm3-TxodHQXJeBa cQGYsa9Rx8n2JOscJxiN9I4130 assertion
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has publication info: NP67317.RAQLU Wm3-TxodHQXJeBa cQGYsa9Rx8n2JOscJxiN9I4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67317.RAQLU Wm3-TxodHQXJeBa cQGYsa9Rx8n2JOscJxiN9I4130 assertion
type: Assertion
description: [D2 dopamine receptor gene polymorphisms among African-Americans and Mexican-Americans: a lung cancer 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/11045783
was generated by: ECO_0000203

NP67318.RAb9tAY5TFfzw1foyyvTZXQNNjZw1p5dn0ls7fcf6ciYI
has assertion: NP67318.RAb9tAY5TFfzw1foyyvTZXQNNjZw1p5dn0ls7fcf6ciYI130 assertion
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has publication info: NP67318.RAb9tAY5TFfzw1foyyvTZXQNNjZw1p5dn0ls7fcf6ciYI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67318.RAb9tAY5TFfzw1foyyvTZXQNNjZw1p5dn0ls7fcf6ciYI130 assertion
type: Assertion
description: [In contrast to controls, no association was found between the DRD2 genotypes and smoking among lung 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/12482370
was generated by: ECO_0000203

NP67319.RAZm ClNTDpZq1Vc2kDj0mY-9uJj7ShdJ35hh Jx98BOA
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has publication info: NP67319.RAZm ClNTDpZq1Vc2kDj0mY-9uJj7ShdJ35hh Jx98BOA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67319.RAZm ClNTDpZq1Vc2kDj0mY-9uJj7ShdJ35hh Jx98BOA130 assertion
type: Assertion
description: [The dopamine receptor/transport gene polymorphisms are associated with the risk of NSCLC among smokers. The data show that the polymorphisms resulting in lower dopamine bioavailability were associated with increased risk of NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17175058
was generated by: ECO_0000203

NP67321.RAewOzHtCH0cRZVEwwWA39Ad7l0Wdsm8cZMleVz0-AF1A
has assertion: NP67321.RAewOzHtCH0cRZVEwwWA39Ad7l0Wdsm8cZMleVz0-AF1A130 assertion
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has publication info: NP67321.RAewOzHtCH0cRZVEwwWA39Ad7l0Wdsm8cZMleVz0-AF1A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67321.RAewOzHtCH0cRZVEwwWA39Ad7l0Wdsm8cZMleVz0-AF1A130 assertion
type: Assertion
description: [These findings suggest that C-reactive protein plays a role in development of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16854501
was generated by: ECO_0000203

NP67329.RAVK75F0xPijPeuv-zG5QMjO0rx1k6r-GOCiXDi4nYD-c
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has provenance: NP67329.RAVK75F0xPijPeuv-zG5QMjO0rx1k6r-GOCiXDi4nYD-c130 provenance
has publication info: NP67329.RAVK75F0xPijPeuv-zG5QMjO0rx1k6r-GOCiXDi4nYD-c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67329.RAVK75F0xPijPeuv-zG5QMjO0rx1k6r-GOCiXDi4nYD-c130 assertion
type: Assertion
description: [The aims of the study were as follows: (1) To identify the differences in spinal body mass density (BMD) in relation to polymorphism in vitamin D receptor (VDR) and estrogen receptor-alpha (ERalpha) genes in untreated women with postmenopausal osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19903038
was generated by: ECO_0000203

NP67336.RAVLEnBIBp30Ch9zE6wun1LOKs4NzIeoI3sDloMecqstU
has assertion: NP67336.RAVLEnBIBp30Ch9zE6wun1LOKs4NzIeoI3sDloMecqstU130 assertion
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has publication info: NP67336.RAVLEnBIBp30Ch9zE6wun1LOKs4NzIeoI3sDloMecqstU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67336.RAVLEnBIBp30Ch9zE6wun1LOKs4NzIeoI3sDloMecqstU130 assertion
type: Assertion
description: [Our aim was to evaluate the effect of four hemostatic genetic variants, namely fibrinogen-beta-455G/A, factor XIII (FXIII) V34L, plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphisms and factor V Leiden (FVL) mutation on survival of critically ill patients with severe sepsis or septic shock.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20051843
was generated by: ECO_0000203

NP67337.RARg038DdQI19g9pBIYT5pqZmonDe6dTBLZXSP2-ARoAs
has assertion: NP67337.RARg038DdQI19g9pBIYT5pqZmonDe6dTBLZXSP2-ARoAs130 assertion
has provenance: NP67337.RARg038DdQI19g9pBIYT5pqZmonDe6dTBLZXSP2-ARoAs130 provenance
has publication info: NP67337.RARg038DdQI19g9pBIYT5pqZmonDe6dTBLZXSP2-ARoAs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67337.RARg038DdQI19g9pBIYT5pqZmonDe6dTBLZXSP2-ARoAs130 assertion
type: Assertion
description: [Candidate gene association study of type 2 diabetes in a nested case-control study of the EPIC-Potsdam cohort - role of fat assimilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17266179
was generated by: ECO_0000203

NP67339.RAWaLAm3J-N5OjUjYTNMUloB5vbn8iotwPRGGLxYZc0d0
has assertion: NP67339.RAWaLAm3J-N5OjUjYTNMUloB5vbn8iotwPRGGLxYZc0d0130 assertion
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has publication info: NP67339.RAWaLAm3J-N5OjUjYTNMUloB5vbn8iotwPRGGLxYZc0d0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67339.RAWaLAm3J-N5OjUjYTNMUloB5vbn8iotwPRGGLxYZc0d0130 assertion
type: Assertion
description: [Carriers of 92Asn had increased risk of MI in CARE and increased odds of CHD in WOSCOPS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17008591
was generated by: ECO_0000203

NP67344.RAVOXaFpi2wwY2ikntip4sRagxkO0z ZQLfoGoqK07F88
has assertion: NP67344.RAVOXaFpi2wwY2ikntip4sRagxkO0z ZQLfoGoqK07F88130 assertion
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67344.RAVOXaFpi2wwY2ikntip4sRagxkO0z ZQLfoGoqK07F88130 assertion
type: Assertion
description: [FKBP52 is likely to play a role in growth and development of the male genitalia, since it is expressed in the genital skin of prepubertal boys; however alterations in the sequence and in the expression of the FKBP4 gene are not a common cause of non-syndromic hypospadias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17343741
was generated by: ECO_0000203

NP67349.RAdDjpjqKuvn8n4hyflG-strMBjeYdAo VUDdbAmVLEh8
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has publication info: NP67349.RAdDjpjqKuvn8n4hyflG-strMBjeYdAo VUDdbAmVLEh8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67349.RAdDjpjqKuvn8n4hyflG-strMBjeYdAo VUDdbAmVLEh8130 assertion
type: Assertion
description: [Common variants conferring risk of schizophrenia: a pathway analysis of GWAS data.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20659789
was generated by: ECO_0000203

NP67352.RAV1XtN0voj4Ii8XLlSE1zIA6mSMKGX2S8PFmi0c3pmKQ
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67352.RAV1XtN0voj4Ii8XLlSE1zIA6mSMKGX2S8PFmi0c3pmKQ130 assertion
type: Assertion
description: [Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16450403
was generated by: ECO_0000203

NP67353.RAY9oJkUeqFsfTht4ldc0kvXeHmpmTL4UM8c5ve tZXIA
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67353.RAY9oJkUeqFsfTht4ldc0kvXeHmpmTL4UM8c5ve tZXIA130 assertion
type: Assertion
description: [The C allele in the CX37 gene might be associated with the susceptibility to CAD and potentially plays an important role in the manifestation of coronary atherosclerosis among 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/17418016
was generated by: ECO_0000203

NP67354.RAddyPvAs3uAmjOgZQqzYawjdLF4YZ6bYPMatdlk7D2es
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67354.RAddyPvAs3uAmjOgZQqzYawjdLF4YZ6bYPMatdlk7D2es130 assertion
type: Assertion
description: [GNAS1 T393C is a novel independent host factor for disease progression in patients with ICC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17356712
was generated by: ECO_0000203

NP67355.RATZIzv9-wu8OAz-rmyTUmnrqyDTv9Te36M1y4iUyR9rA
has assertion: NP67355.RATZIzv9-wu8OAz-rmyTUmnrqyDTv9Te36M1y4iUyR9rA130 assertion
has provenance: NP67355.RATZIzv9-wu8OAz-rmyTUmnrqyDTv9Te36M1y4iUyR9rA130 provenance
has publication info: NP67355.RATZIzv9-wu8OAz-rmyTUmnrqyDTv9Te36M1y4iUyR9rA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67355.RATZIzv9-wu8OAz-rmyTUmnrqyDTv9Te36M1y4iUyR9rA130 assertion
type: Assertion
description: [Meal-unrelated dyspepsia in a U.S. community study is associated with the homozygous 825T or C alleles of GNbeta3 protein. Candidate genes controlling adrenergic, serotonergic, and CCKergic functions do not appear to be associated with dyspepsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16464220
was generated by: ECO_0000203

NP67360.RAYVijt11-zNQdv7yF6qxMA1BDc3HBAAsZcjDTihFvx9g
has assertion: NP67360.RAYVijt11-zNQdv7yF6qxMA1BDc3HBAAsZcjDTihFvx9g130 assertion
has provenance: NP67360.RAYVijt11-zNQdv7yF6qxMA1BDc3HBAAsZcjDTihFvx9g130 provenance
has publication info: NP67360.RAYVijt11-zNQdv7yF6qxMA1BDc3HBAAsZcjDTihFvx9g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67360.RAYVijt11-zNQdv7yF6qxMA1BDc3HBAAsZcjDTihFvx9g130 assertion
type: Assertion
description: [Association of the human kainate receptor GluR7 gene (GRIK3) with recurrent 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/16958029
was generated by: ECO_0000203

NP67364.RAThLljJrAd3-aezD7adE6kjrBVW8 BcCUoTB8214nX34
has assertion: NP67364.RAThLljJrAd3-aezD7adE6kjrBVW8 BcCUoTB8214nX34130 assertion
has provenance: NP67364.RAThLljJrAd3-aezD7adE6kjrBVW8 BcCUoTB8214nX34130 provenance
has publication info: NP67364.RAThLljJrAd3-aezD7adE6kjrBVW8 BcCUoTB8214nX34130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67364.RAThLljJrAd3-aezD7adE6kjrBVW8 BcCUoTB8214nX34130 assertion
type: Assertion
description: [Genetic polymorphisms in GSTM1, GSTT1, GSTP1, GSTM3 and the susceptibility to gallbladder cancer in North India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16760134
was generated by: ECO_0000203

NP67367.RAbnCjKGjRy9MfQzoEH38VC6EgEaan4mwwXd5SRagxkAM
has assertion: NP67367.RAbnCjKGjRy9MfQzoEH38VC6EgEaan4mwwXd5SRagxkAM130 assertion
has provenance: NP67367.RAbnCjKGjRy9MfQzoEH38VC6EgEaan4mwwXd5SRagxkAM130 provenance
has publication info: NP67367.RAbnCjKGjRy9MfQzoEH38VC6EgEaan4mwwXd5SRagxkAM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67367.RAbnCjKGjRy9MfQzoEH38VC6EgEaan4mwwXd5SRagxkAM130 assertion
type: Assertion
description: [The finding that haptoglobin 2-2 genotype is a risk factor for anaemia in children in a malaria-endemic area may reflect the reduced ability of the Hp2-2 polymer to scavenge free haemoglobin-iron following malaria-induced haemolysis. The magnitude of the effect of haptoglobin genotype (4 g/l Hb difference, p = 0.0009) was comparable to that of G6PD deficiency or HbAS (3 g/l difference, p = 0.03; and 2 g/l difference, p = 0.68, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16637741
was generated by: ECO_0000203

NP67369.RAf4WYrlezCPDeqVYta RPFaJkBsaVnhdDndMqs-JPgNQ
has assertion: NP67369.RAf4WYrlezCPDeqVYta RPFaJkBsaVnhdDndMqs-JPgNQ130 assertion
has provenance: NP67369.RAf4WYrlezCPDeqVYta RPFaJkBsaVnhdDndMqs-JPgNQ130 provenance
has publication info: NP67369.RAf4WYrlezCPDeqVYta RPFaJkBsaVnhdDndMqs-JPgNQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67369.RAf4WYrlezCPDeqVYta RPFaJkBsaVnhdDndMqs-JPgNQ130 assertion
type: Assertion
description: [Serum ferritin concentrations and body iron stores in a multicenter, multiethnic primary-care 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/18429050
was generated by: ECO_0000203

NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng
has assertion: NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130 assertion
has provenance: NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130 provenance
has publication info: NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130 assertion
type: Assertion
description: [HJV p.A310G polymorphism and two intronic variants were found, but none of these alterations were associated with digenic inheritance with the HFE gene. Our data indicate that HJV and HAMP functional mutations are not frequent in these 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/21039223
was generated by: ECO_0000203

NP67372.RAV9H53-Ctq8WD2qN3WwnS-Nse OaCROAUxs845bMK4to
has assertion: NP67372.RAV9H53-Ctq8WD2qN3WwnS-Nse OaCROAUxs845bMK4to130 assertion
has provenance: NP67372.RAV9H53-Ctq8WD2qN3WwnS-Nse OaCROAUxs845bMK4to130 provenance
has publication info: NP67372.RAV9H53-Ctq8WD2qN3WwnS-Nse OaCROAUxs845bMK4to130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67372.RAV9H53-Ctq8WD2qN3WwnS-Nse OaCROAUxs845bMK4to130 assertion
type: Assertion
description: [Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11943417
was generated by: ECO_0000203

NP67376.RAayVaS4F1LKHqZELucXIXptFI04zsKrOMlpIMCEdnFjY
has assertion: NP67376.RAayVaS4F1LKHqZELucXIXptFI04zsKrOMlpIMCEdnFjY130 assertion
has provenance: NP67376.RAayVaS4F1LKHqZELucXIXptFI04zsKrOMlpIMCEdnFjY130 provenance
has publication info: NP67376.RAayVaS4F1LKHqZELucXIXptFI04zsKrOMlpIMCEdnFjY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67376.RAayVaS4F1LKHqZELucXIXptFI04zsKrOMlpIMCEdnFjY130 assertion
type: Assertion
description: [Association between ulcerative growth and hypoxia inducible factor-1alpha polymorphisms 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/16865676
was generated by: ECO_0000203

NP67379.RAZsZuGpSrzWvXhfbQzY4i8Cne43i1j2SvFJrbmHva1lI
has assertion: NP67379.RAZsZuGpSrzWvXhfbQzY4i8Cne43i1j2SvFJrbmHva1lI130 assertion
has provenance: NP67379.RAZsZuGpSrzWvXhfbQzY4i8Cne43i1j2SvFJrbmHva1lI130 provenance
has publication info: NP67379.RAZsZuGpSrzWvXhfbQzY4i8Cne43i1j2SvFJrbmHva1lI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67379.RAZsZuGpSrzWvXhfbQzY4i8Cne43i1j2SvFJrbmHva1lI130 assertion
type: Assertion
description: [These results suggest that HIF1A1 C1772T and G1790A polymorphisms are not involved in the progression or metastasis of 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/20651398
was generated by: ECO_0000203

NP67385.RAVMSTkCqWyHbdNSy5kz96sCuxRHBGtsindCGxtlh0x-s
has assertion: NP67385.RAVMSTkCqWyHbdNSy5kz96sCuxRHBGtsindCGxtlh0x-s130 assertion
has provenance: NP67385.RAVMSTkCqWyHbdNSy5kz96sCuxRHBGtsindCGxtlh0x-s130 provenance
has publication info: NP67385.RAVMSTkCqWyHbdNSy5kz96sCuxRHBGtsindCGxtlh0x-s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67385.RAVMSTkCqWyHbdNSy5kz96sCuxRHBGtsindCGxtlh0x-s130 assertion
type: Assertion
description: [HLA typing in Indian children with NS helps to predict relapse frequency and steroid resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17180363
was generated by: ECO_0000203

NP67387.RAWzkCMSdPEwYTu8AFt0Qch5QjwzooL36Ev173cqNyUjU
has assertion: NP67387.RAWzkCMSdPEwYTu8AFt0Qch5QjwzooL36Ev173cqNyUjU130 assertion
has provenance: NP67387.RAWzkCMSdPEwYTu8AFt0Qch5QjwzooL36Ev173cqNyUjU130 provenance
has publication info: NP67387.RAWzkCMSdPEwYTu8AFt0Qch5QjwzooL36Ev173cqNyUjU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67387.RAWzkCMSdPEwYTu8AFt0Qch5QjwzooL36Ev173cqNyUjU130 assertion
type: Assertion
description: [According to HLA typing, the results support the hypothesis that IgM nephropathy is a different entity from minimal change nephrotic 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/19390203
was generated by: ECO_0000203

NP67403.RAfoEMlEDZPqZq1Rcb3lMckHEVkxjOsbjKrrH8u3 2 Ec
has assertion: NP67403.RAfoEMlEDZPqZq1Rcb3lMckHEVkxjOsbjKrrH8u3 2 Ec130 assertion
has provenance: NP67403.RAfoEMlEDZPqZq1Rcb3lMckHEVkxjOsbjKrrH8u3 2 Ec130 provenance
has publication info: NP67403.RAfoEMlEDZPqZq1Rcb3lMckHEVkxjOsbjKrrH8u3 2 Ec130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67403.RAfoEMlEDZPqZq1Rcb3lMckHEVkxjOsbjKrrH8u3 2 Ec130 assertion
type: Assertion
description: [Our results suggest an important role for HTR3B in major depression in women and also raise the possibility that previously proposed disease-associated SNPs in the HTR3A/B region in Caucasians are in linkage disequilibrium with haplotype block 2 of HTR3B in the Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16487942
was generated by: ECO_0000203

NP67409.RAamMgY83lVIFMDEOk4Gl2VjMkeNFoh1HdX2RJij2l9os
has assertion: NP67409.RAamMgY83lVIFMDEOk4Gl2VjMkeNFoh1HdX2RJij2l9os130 assertion
has provenance: NP67409.RAamMgY83lVIFMDEOk4Gl2VjMkeNFoh1HdX2RJij2l9os130 provenance
has publication info: NP67409.RAamMgY83lVIFMDEOk4Gl2VjMkeNFoh1HdX2RJij2l9os130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67409.RAamMgY83lVIFMDEOk4Gl2VjMkeNFoh1HdX2RJij2l9os130 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

NP67410.RAXoIm KlWCDoV-xMFkBKQmQe1RIF1IqLVZ4e8O7OOug0
has assertion: NP67410.RAXoIm KlWCDoV-xMFkBKQmQe1RIF1IqLVZ4e8O7OOug0130 assertion
has provenance: NP67410.RAXoIm KlWCDoV-xMFkBKQmQe1RIF1IqLVZ4e8O7OOug0130 provenance
has publication info: NP67410.RAXoIm KlWCDoV-xMFkBKQmQe1RIF1IqLVZ4e8O7OOug0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67410.RAXoIm KlWCDoV-xMFkBKQmQe1RIF1IqLVZ4e8O7OOug0130 assertion
type: Assertion
description: [Role of single nucleotide polymorphisms of cytokine genes in spontaneous preterm delivery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17145371
was generated by: ECO_0000203

NP67422.RAfumwETIefnBgopXCsTVoDV7OrT-JoWakVD86anVhc7M
has assertion: NP67422.RAfumwETIefnBgopXCsTVoDV7OrT-JoWakVD86anVhc7M130 assertion
has provenance: NP67422.RAfumwETIefnBgopXCsTVoDV7OrT-JoWakVD86anVhc7M130 provenance
has publication info: NP67422.RAfumwETIefnBgopXCsTVoDV7OrT-JoWakVD86anVhc7M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67422.RAfumwETIefnBgopXCsTVoDV7OrT-JoWakVD86anVhc7M130 assertion
type: Assertion
description: [The carriage of proinflammatory IL-1B-511 and HP vacA m1 genotypes was associated with the development of gastric IM in the 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/16635219
was generated by: ECO_0000203

NP67431.RAZX9qS4QBVo0MLr0MTexlHwwBEFasWVovBGN4053U0lQ
has assertion: NP67431.RAZX9qS4QBVo0MLr0MTexlHwwBEFasWVovBGN4053U0lQ130 assertion
has provenance: NP67431.RAZX9qS4QBVo0MLr0MTexlHwwBEFasWVovBGN4053U0lQ130 provenance
has publication info: NP67431.RAZX9qS4QBVo0MLr0MTexlHwwBEFasWVovBGN4053U0lQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67431.RAZX9qS4QBVo0MLr0MTexlHwwBEFasWVovBGN4053U0lQ130 assertion
type: Assertion
description: [Analysis of the variations in IL-28RA gene and their association with 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/16819289
was generated by: ECO_0000203

NP67432.RATDVPHzwPbxmOb7l9AnDWvEc2gf2P3HkaCqmX3uF6s-s
has assertion: NP67432.RATDVPHzwPbxmOb7l9AnDWvEc2gf2P3HkaCqmX3uF6s-s130 assertion
has provenance: NP67432.RATDVPHzwPbxmOb7l9AnDWvEc2gf2P3HkaCqmX3uF6s-s130 provenance
has publication info: NP67432.RATDVPHzwPbxmOb7l9AnDWvEc2gf2P3HkaCqmX3uF6s-s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67432.RATDVPHzwPbxmOb7l9AnDWvEc2gf2P3HkaCqmX3uF6s-s130 assertion
type: Assertion
description: [Cytokine gene polymorphisms can alter the effect of Bacillus Calmette-Gurin (BCG) immunotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16938461
was generated by: ECO_0000203

NP67437.RAdUMR9lwApU0BtX-Rx9JhyrnDb2emPIIBuphmH09mqCI
has assertion: NP67437.RAdUMR9lwApU0BtX-Rx9JhyrnDb2emPIIBuphmH09mqCI130 assertion
has provenance: NP67437.RAdUMR9lwApU0BtX-Rx9JhyrnDb2emPIIBuphmH09mqCI130 provenance
has publication info: NP67437.RAdUMR9lwApU0BtX-Rx9JhyrnDb2emPIIBuphmH09mqCI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67437.RAdUMR9lwApU0BtX-Rx9JhyrnDb2emPIIBuphmH09mqCI130 assertion
type: Assertion
description: [We investigated 30 patients with idiopathic pulmonary fibrosis (IPF) and 103 healthy volunteers for the cytokines polymorphisms of the IL-1alpha, IL-1beta, IL-1R, IL-1RA, IL-2, IL-4, IL-6, IL-10, IL-12, tumor necrosis factor-alpha, interferon-gamma, transforming growth factor-beta, IL-1beta, IL-2, IL-4, and IL-4RA 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/16573560
was generated by: ECO_0000203

NP67438.RAXW4fqVmjge7Xr1DI4Yzpgmrtxi5uKsN42ZhjlLuy1G0
has assertion: NP67438.RAXW4fqVmjge7Xr1DI4Yzpgmrtxi5uKsN42ZhjlLuy1G0130 assertion
has provenance: NP67438.RAXW4fqVmjge7Xr1DI4Yzpgmrtxi5uKsN42ZhjlLuy1G0130 provenance
has publication info: NP67438.RAXW4fqVmjge7Xr1DI4Yzpgmrtxi5uKsN42ZhjlLuy1G0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67438.RAXW4fqVmjge7Xr1DI4Yzpgmrtxi5uKsN42ZhjlLuy1G0130 assertion
type: Assertion
description: [The aims of the present case-control study were to examine polymorphisms in the IL-6, transforming growth factor (TGF)-beta 1, tumour necrosis factor (TNF)-alpha and interleukin-1 (IL-1)Ra genes in patients with IPF (n = 22) -compared to healthy controls (n = 140).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15030461
was generated by: ECO_0000203

NP67440.RARfuAvqZ3P8HWgT-vST7nn8GeXfVYFKmWHM8x9-qrd E
has assertion: NP67440.RARfuAvqZ3P8HWgT-vST7nn8GeXfVYFKmWHM8x9-qrd E130 assertion
has provenance: NP67440.RARfuAvqZ3P8HWgT-vST7nn8GeXfVYFKmWHM8x9-qrd E130 provenance
has publication info: NP67440.RARfuAvqZ3P8HWgT-vST7nn8GeXfVYFKmWHM8x9-qrd E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67440.RARfuAvqZ3P8HWgT-vST7nn8GeXfVYFKmWHM8x9-qrd E130 assertion
type: Assertion
description: [Crosstalk between the 2 chemokines CXCL8 and CCL5 may contribute to the 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/17599774
was generated by: ECO_0000203

NP67456.RAVglFJV2hiF7MzzcZqEr Y7ovma68O7K8xZwIb2t50sY
has assertion: NP67456.RAVglFJV2hiF7MzzcZqEr Y7ovma68O7K8xZwIb2t50sY130 assertion
has provenance: NP67456.RAVglFJV2hiF7MzzcZqEr Y7ovma68O7K8xZwIb2t50sY130 provenance
has publication info: NP67456.RAVglFJV2hiF7MzzcZqEr Y7ovma68O7K8xZwIb2t50sY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67456.RAVglFJV2hiF7MzzcZqEr Y7ovma68O7K8xZwIb2t50sY130 assertion
type: Assertion
description: [were obtained with haplotype 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/16957554
was generated by: ECO_0000203

NP67460.RAW H1QkHOix5tXbQYSSPaSG9gxjmnuhQf e2lTqamujQ
has assertion: NP67460.RAW H1QkHOix5tXbQYSSPaSG9gxjmnuhQf e2lTqamujQ130 assertion
has provenance: NP67460.RAW H1QkHOix5tXbQYSSPaSG9gxjmnuhQf e2lTqamujQ130 provenance
has publication info: NP67460.RAW H1QkHOix5tXbQYSSPaSG9gxjmnuhQf e2lTqamujQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67460.RAW H1QkHOix5tXbQYSSPaSG9gxjmnuhQf e2lTqamujQ130 assertion
type: Assertion
description: [Analysis of drug resistance gene polymorphism appears to be an indicator of the response to chemotherapy in advanced 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/16821592
was generated by: ECO_0000203

NP67462.RAXwmnEpwND7POEHXmECtQ9ty3BO3NimVsOg3khnTYRos
has assertion: NP67462.RAXwmnEpwND7POEHXmECtQ9ty3BO3NimVsOg3khnTYRos130 assertion
has provenance: NP67462.RAXwmnEpwND7POEHXmECtQ9ty3BO3NimVsOg3khnTYRos130 provenance
has publication info: NP67462.RAXwmnEpwND7POEHXmECtQ9ty3BO3NimVsOg3khnTYRos130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67462.RAXwmnEpwND7POEHXmECtQ9ty3BO3NimVsOg3khnTYRos130 assertion
type: Assertion
description: [The LRRK2 Gly2385Arg variant is not a significant risk factor for ET 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/18316234
was generated by: ECO_0000203

NP67465.RAU e8tT W5iUEwUDPnyJZ-juwKHDcd33a7m1x9kcHzO0
has assertion: NP67465.RAU e8tT W5iUEwUDPnyJZ-juwKHDcd33a7m1x9kcHzO0130 assertion
has provenance: NP67465.RAU e8tT W5iUEwUDPnyJZ-juwKHDcd33a7m1x9kcHzO0130 provenance
has publication info: NP67465.RAU e8tT W5iUEwUDPnyJZ-juwKHDcd33a7m1x9kcHzO0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67465.RAU e8tT W5iUEwUDPnyJZ-juwKHDcd33a7m1x9kcHzO0130 assertion
type: Assertion
description: [Association of common haplotypes of surfactant protein A1 and A2 (SFTPA1 and SFTPA2) genes with severity of lung disease in cystic fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16429424
was generated by: ECO_0000203

NP67467.RAfheNY9zGTFNVCD rPU0Vnclvb0-Z89YMu UhvV9VYpQ
has assertion: NP67467.RAfheNY9zGTFNVCD rPU0Vnclvb0-Z89YMu UhvV9VYpQ130 assertion
has provenance: NP67467.RAfheNY9zGTFNVCD rPU0Vnclvb0-Z89YMu UhvV9VYpQ130 provenance
has publication info: NP67467.RAfheNY9zGTFNVCD rPU0Vnclvb0-Z89YMu UhvV9VYpQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67467.RAfheNY9zGTFNVCD rPU0Vnclvb0-Z89YMu UhvV9VYpQ130 assertion
type: Assertion
description: [MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic 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/17427193
was generated by: ECO_0000203

NP67475.RAQDQX1ywYwcI2Nm4rrS7depELx4zyp3rps emQ9m6UcQ
has assertion: NP67475.RAQDQX1ywYwcI2Nm4rrS7depELx4zyp3rps emQ9m6UcQ130 assertion
has provenance: NP67475.RAQDQX1ywYwcI2Nm4rrS7depELx4zyp3rps emQ9m6UcQ130 provenance
has publication info: NP67475.RAQDQX1ywYwcI2Nm4rrS7depELx4zyp3rps emQ9m6UcQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67475.RAQDQX1ywYwcI2Nm4rrS7depELx4zyp3rps emQ9m6UcQ130 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

NP67476.RAR0a8V9eT1zwMJF55sLugTRd9P4tdV3bMmCWU-AT7eQ4
has assertion: NP67476.RAR0a8V9eT1zwMJF55sLugTRd9P4tdV3bMmCWU-AT7eQ4130 assertion
has provenance: NP67476.RAR0a8V9eT1zwMJF55sLugTRd9P4tdV3bMmCWU-AT7eQ4130 provenance
has publication info: NP67476.RAR0a8V9eT1zwMJF55sLugTRd9P4tdV3bMmCWU-AT7eQ4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67476.RAR0a8V9eT1zwMJF55sLugTRd9P4tdV3bMmCWU-AT7eQ4130 assertion
type: Assertion
description: [Genetic factors for lone atrial fibrillation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17487426
was generated by: ECO_0000203

NP67484.RAR-0yXEBPA8ArViNYt8nPiz JbRE2TUl416esk4m-R08
has assertion: NP67484.RAR-0yXEBPA8ArViNYt8nPiz JbRE2TUl416esk4m-R08130 assertion
has provenance: NP67484.RAR-0yXEBPA8ArViNYt8nPiz JbRE2TUl416esk4m-R08130 provenance
has publication info: NP67484.RAR-0yXEBPA8ArViNYt8nPiz JbRE2TUl416esk4m-R08130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67484.RAR-0yXEBPA8ArViNYt8nPiz JbRE2TUl416esk4m-R08130 assertion
type: Assertion
description: [Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: 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/17136115
was generated by: ECO_0000203

NP67495.RAYAQPrMITDOkeFefhlcClm50R4S2 xxJjD0edgxTdI0A
has assertion: NP67495.RAYAQPrMITDOkeFefhlcClm50R4S2 xxJjD0edgxTdI0A130 assertion
has provenance: NP67495.RAYAQPrMITDOkeFefhlcClm50R4S2 xxJjD0edgxTdI0A130 provenance
has publication info: NP67495.RAYAQPrMITDOkeFefhlcClm50R4S2 xxJjD0edgxTdI0A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67495.RAYAQPrMITDOkeFefhlcClm50R4S2 xxJjD0edgxTdI0A130 assertion
type: Assertion
description: [TagSNP evaluation for the association of 42 inflammation loci and vascular disease: evidence of IL6, FGB, ALOX5, NFKBIA, and IL4R loci effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17115186
was generated by: ECO_0000203

NP67498.RAe1o7XLGQw4aIZRa5 nwfSY8qVt5qVN7JVub07GSNTBM
has assertion: NP67498.RAe1o7XLGQw4aIZRa5 nwfSY8qVt5qVN7JVub07GSNTBM130 assertion
has provenance: NP67498.RAe1o7XLGQw4aIZRa5 nwfSY8qVt5qVN7JVub07GSNTBM130 provenance
has publication info: NP67498.RAe1o7XLGQw4aIZRa5 nwfSY8qVt5qVN7JVub07GSNTBM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67498.RAe1o7XLGQw4aIZRa5 nwfSY8qVt5qVN7JVub07GSNTBM130 assertion
type: Assertion
description: [Genetic variants of nNOS, but not iNOS, may be biomarkers for susceptibility to CM, and the risk of CM associated with sunburns and moles may be modulated by nNOS variant 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/17328085
was generated by: ECO_0000203

NP67505.RAX-NgGx6jPB9xdUVVfK-QIYQYN4GT7m03h-2mhN4Gyuw
has assertion: NP67505.RAX-NgGx6jPB9xdUVVfK-QIYQYN4GT7m03h-2mhN4Gyuw130 assertion
has provenance: NP67505.RAX-NgGx6jPB9xdUVVfK-QIYQYN4GT7m03h-2mhN4Gyuw130 provenance
has publication info: NP67505.RAX-NgGx6jPB9xdUVVfK-QIYQYN4GT7m03h-2mhN4Gyuw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67505.RAX-NgGx6jPB9xdUVVfK-QIYQYN4GT7m03h-2mhN4Gyuw130 assertion
type: Assertion
description: [Using Phase II HapMap data, we demonstrate that there are a set of polymorphisms, spanning genes from prolyl 4-hydroxylase (P4HA2) through interferon regulatory factor 1 (IRF1) with equivalent statistical evidence of association to the reported SLC22A4 variant and that each, by itself, could entirely explain the IBD5 association to 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/17213842
was generated by: ECO_0000203

NP67506.RASA0Lz7Y1kkLftb23ZBP23ojY6boVFjGWjtUof52FmLY
has assertion: NP67506.RASA0Lz7Y1kkLftb23ZBP23ojY6boVFjGWjtUof52FmLY130 assertion
has provenance: NP67506.RASA0Lz7Y1kkLftb23ZBP23ojY6boVFjGWjtUof52FmLY130 provenance
has publication info: NP67506.RASA0Lz7Y1kkLftb23ZBP23ojY6boVFjGWjtUof52FmLY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67506.RASA0Lz7Y1kkLftb23ZBP23ojY6boVFjGWjtUof52FmLY130 assertion
type: Assertion
description: [PARP-1 -410 and PARP-1 -1672 haplotypes were associated with an increased risk for AD (global haplotype association p value=0.019), and, in addition, PARP-1 haplotypes increased the risk of AD by interaction with the IL-1A -889 allele 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/17290104
was generated by: ECO_0000203

NP67507.RAXQySrhkUfnXYCrgesDNsDgYlYp3-ME 3Zb0ROTQn44Y
has assertion: NP67507.RAXQySrhkUfnXYCrgesDNsDgYlYp3-ME 3Zb0ROTQn44Y130 assertion
has provenance: NP67507.RAXQySrhkUfnXYCrgesDNsDgYlYp3-ME 3Zb0ROTQn44Y130 provenance
has publication info: NP67507.RAXQySrhkUfnXYCrgesDNsDgYlYp3-ME 3Zb0ROTQn44Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67507.RAXQySrhkUfnXYCrgesDNsDgYlYp3-ME 3Zb0ROTQn44Y130 assertion
type: Assertion
description: [Evaluation of the poly(ADP-ribose) polymerase-1 gene variants 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/20486200
was generated by: ECO_0000203

NP67513.RAZC2xOUR2AJoGQICdIK3NpesubgxZRMx5q7eJyFr-RB8
has assertion: NP67513.RAZC2xOUR2AJoGQICdIK3NpesubgxZRMx5q7eJyFr-RB8130 assertion
has provenance: NP67513.RAZC2xOUR2AJoGQICdIK3NpesubgxZRMx5q7eJyFr-RB8130 provenance
has publication info: NP67513.RAZC2xOUR2AJoGQICdIK3NpesubgxZRMx5q7eJyFr-RB8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67513.RAZC2xOUR2AJoGQICdIK3NpesubgxZRMx5q7eJyFr-RB8130 assertion
type: Assertion
description: [A91V perforin variation in healthy subjects and FHLH 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/16611257
was generated by: ECO_0000203

NP67521.RATHHTc6 1WGqd7t0nRoDZsWAiHN8BP2Aqh2oam7ue4hE
has assertion: NP67521.RATHHTc6 1WGqd7t0nRoDZsWAiHN8BP2Aqh2oam7ue4hE130 assertion
has provenance: NP67521.RATHHTc6 1WGqd7t0nRoDZsWAiHN8BP2Aqh2oam7ue4hE130 provenance
has publication info: NP67521.RATHHTc6 1WGqd7t0nRoDZsWAiHN8BP2Aqh2oam7ue4hE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67521.RATHHTc6 1WGqd7t0nRoDZsWAiHN8BP2Aqh2oam7ue4hE130 assertion
type: Assertion
description: [from this study provide evidence for associations between variants in genes in the DSBR pathway and bladder cancers risk that warrant replication in other study 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/17557904
was generated by: ECO_0000203

NP67523.RAV 9ydAXeZXMkMwBbP5qnYFSX-MYPGYxkXIu7VXGOMa4
has assertion: NP67523.RAV 9ydAXeZXMkMwBbP5qnYFSX-MYPGYxkXIu7VXGOMa4130 assertion
has provenance: NP67523.RAV 9ydAXeZXMkMwBbP5qnYFSX-MYPGYxkXIu7VXGOMa4130 provenance
has publication info: NP67523.RAV 9ydAXeZXMkMwBbP5qnYFSX-MYPGYxkXIu7VXGOMa4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67523.RAV 9ydAXeZXMkMwBbP5qnYFSX-MYPGYxkXIu7VXGOMa4130 assertion
type: Assertion
description: [Genetic polymorphisms in 85 DNA repair genes and bladder 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/19237606
was generated by: ECO_0000203

NP67527.RAcenY5dQNRGDh LOWVVky-DZ0CFahgaE2KpvieUBtunc
has assertion: NP67527.RAcenY5dQNRGDh LOWVVky-DZ0CFahgaE2KpvieUBtunc130 assertion
has provenance: NP67527.RAcenY5dQNRGDh LOWVVky-DZ0CFahgaE2KpvieUBtunc130 provenance
has publication info: NP67527.RAcenY5dQNRGDh LOWVVky-DZ0CFahgaE2KpvieUBtunc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67527.RAcenY5dQNRGDh LOWVVky-DZ0CFahgaE2KpvieUBtunc130 assertion
type: Assertion
description: [our findings suggest that variants within the S100B gene predispose to a psychotic subtype of BPAD, possibly via alteration of gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17525977
was generated by: ECO_0000203

NP67528.RAacTSOU2LeH8O8vybw6ZVcs20g4K0rgD8w2L zHKlNQg
has assertion: NP67528.RAacTSOU2LeH8O8vybw6ZVcs20g4K0rgD8w2L zHKlNQg130 assertion
has provenance: NP67528.RAacTSOU2LeH8O8vybw6ZVcs20g4K0rgD8w2L zHKlNQg130 provenance
has publication info: NP67528.RAacTSOU2LeH8O8vybw6ZVcs20g4K0rgD8w2L zHKlNQg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67528.RAacTSOU2LeH8O8vybw6ZVcs20g4K0rgD8w2L zHKlNQg130 assertion
type: Assertion
description: [In conclusion, in the present study population, SCARB1 polymorphisms not only show associations with plasma levels of total and low-density lipoprotein cholesterol, respectively, but also with the risk for PAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17618962
was generated by: ECO_0000203

NP67532.RAUEWS Lv 9DaT73 RyYX4i-4enxOmzrXoLa3ez2pmA20
has assertion: NP67532.RAUEWS Lv 9DaT73 RyYX4i-4enxOmzrXoLa3ez2pmA20130 assertion
has provenance: NP67532.RAUEWS Lv 9DaT73 RyYX4i-4enxOmzrXoLa3ez2pmA20130 provenance
has publication info: NP67532.RAUEWS Lv 9DaT73 RyYX4i-4enxOmzrXoLa3ez2pmA20130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67532.RAUEWS Lv 9DaT73 RyYX4i-4enxOmzrXoLa3ez2pmA20130 assertion
type: Assertion
description: [No significant differences were observed in the F206L polymorphism of L-selectin, or the G241R and E469K polymorphisms in the ICAM-1 gene in 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/16916660
was generated by: ECO_0000203

NP67533.RATjZKmTj9boF6ZX8sqFAtXuGwAecg 1220gw6zJsIWCk
has assertion: NP67533.RATjZKmTj9boF6ZX8sqFAtXuGwAecg 1220gw6zJsIWCk130 assertion
has provenance: NP67533.RATjZKmTj9boF6ZX8sqFAtXuGwAecg 1220gw6zJsIWCk130 provenance
has publication info: NP67533.RATjZKmTj9boF6ZX8sqFAtXuGwAecg 1220gw6zJsIWCk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67533.RATjZKmTj9boF6ZX8sqFAtXuGwAecg 1220gw6zJsIWCk130 assertion
type: Assertion
description: [To further characterize these parameters, the present study analyzed the expression of three isoforms of septin 3 (A, B, and C) in fetal and adult human brains and polymorphism of the septin 3 exon 11 microsatellite in control, pure Alzheimer's disease (AD), Lewy body variant (LBV) of AD, 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/15200238
was generated by: ECO_0000203

NP67536.RAWujjbNTaAL0Ol0O8LWOd-ArzI5yBxkBDP9jrUqIXHHY
has assertion: NP67536.RAWujjbNTaAL0Ol0O8LWOd-ArzI5yBxkBDP9jrUqIXHHY130 assertion
has provenance: NP67536.RAWujjbNTaAL0Ol0O8LWOd-ArzI5yBxkBDP9jrUqIXHHY130 provenance
has publication info: NP67536.RAWujjbNTaAL0Ol0O8LWOd-ArzI5yBxkBDP9jrUqIXHHY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67536.RAWujjbNTaAL0Ol0O8LWOd-ArzI5yBxkBDP9jrUqIXHHY130 assertion
type: Assertion
description: [Recent studies have proposed that the serine protease inhibitor E2 (SERPINE2) was a novel susceptibility gene for chronic obstructive pulmonary disease (COPD) in 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/19604412
was generated by: ECO_0000203

NP67537.RASOprlYYA6FwahIqa3qL4QNvwUfdSL-PodDRBuo47Hvc
has assertion: NP67537.RASOprlYYA6FwahIqa3qL4QNvwUfdSL-PodDRBuo47Hvc130 assertion
has provenance: NP67537.RASOprlYYA6FwahIqa3qL4QNvwUfdSL-PodDRBuo47Hvc130 provenance
has publication info: NP67537.RASOprlYYA6FwahIqa3qL4QNvwUfdSL-PodDRBuo47Hvc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67537.RASOprlYYA6FwahIqa3qL4QNvwUfdSL-PodDRBuo47Hvc130 assertion
type: Assertion
description: [SERPINE2 polymorphisms and chronic obstructive pulmonary 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/19949669
was generated by: ECO_0000203

NP67541.RATLiC46dL3lwOQ8JPJ0wLX4HrTb-DfU6rtw1i-LvJqoo
has assertion: NP67541.RATLiC46dL3lwOQ8JPJ0wLX4HrTb-DfU6rtw1i-LvJqoo130 assertion
has provenance: NP67541.RATLiC46dL3lwOQ8JPJ0wLX4HrTb-DfU6rtw1i-LvJqoo130 provenance
has publication info: NP67541.RATLiC46dL3lwOQ8JPJ0wLX4HrTb-DfU6rtw1i-LvJqoo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67541.RATLiC46dL3lwOQ8JPJ0wLX4HrTb-DfU6rtw1i-LvJqoo130 assertion
type: Assertion
description: [Analysis of the SIM1 contribution to polygenic obesity 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/20075856
was generated by: ECO_0000203

NP67542.RAdDnScpbZE6gO-L-NgSb3sTJQZTnAImQSPMW9bFVFeNM
has assertion: NP67542.RAdDnScpbZE6gO-L-NgSb3sTJQZTnAImQSPMW9bFVFeNM130 assertion
has provenance: NP67542.RAdDnScpbZE6gO-L-NgSb3sTJQZTnAImQSPMW9bFVFeNM130 provenance
has publication info: NP67542.RAdDnScpbZE6gO-L-NgSb3sTJQZTnAImQSPMW9bFVFeNM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67542.RAdDnScpbZE6gO-L-NgSb3sTJQZTnAImQSPMW9bFVFeNM130 assertion
type: Assertion
description: [this report does not support a substantial overall association between the evaluated polymorphisms in the one-carbon metabolism pathway 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/17311260
was generated by: ECO_0000203

NP67543.RAYhQAQez3--ACSW-iBJmrZwoPN0ups OgjAvHfVxxrCE
has assertion: NP67543.RAYhQAQez3--ACSW-iBJmrZwoPN0ups OgjAvHfVxxrCE130 assertion
has provenance: NP67543.RAYhQAQez3--ACSW-iBJmrZwoPN0ups OgjAvHfVxxrCE130 provenance
has publication info: NP67543.RAYhQAQez3--ACSW-iBJmrZwoPN0ups OgjAvHfVxxrCE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67543.RAYhQAQez3--ACSW-iBJmrZwoPN0ups OgjAvHfVxxrCE130 assertion
type: Assertion
description: [GABA(A) receptor beta isoform protein expression in human alcoholic brain: interaction with 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/16766085
was generated by: ECO_0000203

NP67544.RAW7v gN0hsZKCwmgMsSsiBB7rwRkGNvuBeHredD5DPVQ
has assertion: NP67544.RAW7v gN0hsZKCwmgMsSsiBB7rwRkGNvuBeHredD5DPVQ130 assertion
has provenance: NP67544.RAW7v gN0hsZKCwmgMsSsiBB7rwRkGNvuBeHredD5DPVQ130 provenance
has publication info: NP67544.RAW7v gN0hsZKCwmgMsSsiBB7rwRkGNvuBeHredD5DPVQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67544.RAW7v gN0hsZKCwmgMsSsiBB7rwRkGNvuBeHredD5DPVQ130 assertion
type: Assertion
description: [Synergistic association of mitochondrial uncoupling protein (UCP) genes 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/17066476
was generated by: ECO_0000203

NP67546.RAegWMQbW2BrrfI 6Bw0ne5T-XtU8IQtpOOsS6YVzQF7w
has assertion: NP67546.RAegWMQbW2BrrfI 6Bw0ne5T-XtU8IQtpOOsS6YVzQF7w130 assertion
has provenance: NP67546.RAegWMQbW2BrrfI 6Bw0ne5T-XtU8IQtpOOsS6YVzQF7w130 provenance
has publication info: NP67546.RAegWMQbW2BrrfI 6Bw0ne5T-XtU8IQtpOOsS6YVzQF7w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67546.RAegWMQbW2BrrfI 6Bw0ne5T-XtU8IQtpOOsS6YVzQF7w130 assertion
type: Assertion
description: [The effect of dopamine D2, D5 receptor and transporter (SLC6A3) polymorphisms on the cue-elicited heroin craving 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/16526040
was generated by: ECO_0000203

NP67547.RAZF 2PY4WijmE4VUsVjqMfM70hrEyait9jCKx-iD5G44
has assertion: NP67547.RAZF 2PY4WijmE4VUsVjqMfM70hrEyait9jCKx-iD5G44130 assertion
has provenance: NP67547.RAZF 2PY4WijmE4VUsVjqMfM70hrEyait9jCKx-iD5G44130 provenance
has publication info: NP67547.RAZF 2PY4WijmE4VUsVjqMfM70hrEyait9jCKx-iD5G44130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67547.RAZF 2PY4WijmE4VUsVjqMfM70hrEyait9jCKx-iD5G44130 assertion
type: Assertion
description: [We performed a genetic association study using four functional polymorphisms of the dopamine receptor 4 (DRD4), dopamine transporter (DAT), mono-amino-oxidase A (MAOA) and cathecol-O-methyl-transferase (COMT) genes in 103 patients with chronic daily headache associated with DA (CDHDA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16930369
was generated by: ECO_0000203

NP67552.RAXBu0w2i9ZaocbRe53ft3J1zQevkmUxmiF9xEaG4DguM
has assertion: NP67552.RAXBu0w2i9ZaocbRe53ft3J1zQevkmUxmiF9xEaG4DguM130 assertion
has provenance: NP67552.RAXBu0w2i9ZaocbRe53ft3J1zQevkmUxmiF9xEaG4DguM130 provenance
has publication info: NP67552.RAXBu0w2i9ZaocbRe53ft3J1zQevkmUxmiF9xEaG4DguM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67552.RAXBu0w2i9ZaocbRe53ft3J1zQevkmUxmiF9xEaG4DguM130 assertion
type: Assertion
description: [When numeric scores were assigned to both the SNP and demographic data, and sequentially combined by a simple algorithm in a risk model, the composite score was found to be linearly related to lung cancer risk with a bimodal distribution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19789190
was generated by: ECO_0000203

NP67555.RAVgyRWIR4NGV-fKhM KWPQFAy27TgZPFWGcdNA-Zy8gI
has assertion: NP67555.RAVgyRWIR4NGV-fKhM KWPQFAy27TgZPFWGcdNA-Zy8gI130 assertion
has provenance: NP67555.RAVgyRWIR4NGV-fKhM KWPQFAy27TgZPFWGcdNA-Zy8gI130 provenance
has publication info: NP67555.RAVgyRWIR4NGV-fKhM KWPQFAy27TgZPFWGcdNA-Zy8gI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67555.RAVgyRWIR4NGV-fKhM KWPQFAy27TgZPFWGcdNA-Zy8gI130 assertion
type: Assertion
description: [In 253 Gilman probable or definite MSA patients, 457 possible, probable, and definite MSA cases and 1472 controls, a frequency difference for the individual tagging SNPs or tag-defined haplotypes was not detected. No effect was observed of polymorphisms on the pathological expression of MSA in pathologically confirmed 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/16543523
was generated by: ECO_0000203

NP67556.RAbMG-TINRoQtp2Y3eBQ0BKmvuGF7OTMG6kG lRXTllEE
has assertion: NP67556.RAbMG-TINRoQtp2Y3eBQ0BKmvuGF7OTMG6kG lRXTllEE130 assertion
has provenance: NP67556.RAbMG-TINRoQtp2Y3eBQ0BKmvuGF7OTMG6kG lRXTllEE130 provenance
has publication info: NP67556.RAbMG-TINRoQtp2Y3eBQ0BKmvuGF7OTMG6kG lRXTllEE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67556.RAbMG-TINRoQtp2Y3eBQ0BKmvuGF7OTMG6kG lRXTllEE130 assertion
type: Assertion
description: [Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19771175
was generated by: ECO_0000203

NP67560.RAdDQzlzg0Dt1rTqOSybQ3nfRHeWYM8V1W3lt0z2l2MAU
has assertion: NP67560.RAdDQzlzg0Dt1rTqOSybQ3nfRHeWYM8V1W3lt0z2l2MAU130 assertion
has provenance: NP67560.RAdDQzlzg0Dt1rTqOSybQ3nfRHeWYM8V1W3lt0z2l2MAU130 provenance
has publication info: NP67560.RAdDQzlzg0Dt1rTqOSybQ3nfRHeWYM8V1W3lt0z2l2MAU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67560.RAdDQzlzg0Dt1rTqOSybQ3nfRHeWYM8V1W3lt0z2l2MAU130 assertion
type: Assertion
description: [Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset 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/17373700
was generated by: ECO_0000203

NP67568.RAXH0eI522FgE83ct4al7Yan90XtNx6RPSmf7KUBIlV6A
has assertion: NP67568.RAXH0eI522FgE83ct4al7Yan90XtNx6RPSmf7KUBIlV6A130 assertion
has provenance: NP67568.RAXH0eI522FgE83ct4al7Yan90XtNx6RPSmf7KUBIlV6A130 provenance
has publication info: NP67568.RAXH0eI522FgE83ct4al7Yan90XtNx6RPSmf7KUBIlV6A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67568.RAXH0eI522FgE83ct4al7Yan90XtNx6RPSmf7KUBIlV6A130 assertion
type: Assertion
description: [The neuropeptide genes TAC1, TAC3, TAC4, VIP and PACAP(ADCYAP1), and susceptibility to 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/17175032
was generated by: ECO_0000203

NP67569.RAdQYHQSJdd0j8ITtrkC-xZv9Oe7oBWY76FB4PpRxoQNI
has assertion: NP67569.RAdQYHQSJdd0j8ITtrkC-xZv9Oe7oBWY76FB4PpRxoQNI130 assertion
has provenance: NP67569.RAdQYHQSJdd0j8ITtrkC-xZv9Oe7oBWY76FB4PpRxoQNI130 provenance
has publication info: NP67569.RAdQYHQSJdd0j8ITtrkC-xZv9Oe7oBWY76FB4PpRxoQNI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67569.RAdQYHQSJdd0j8ITtrkC-xZv9Oe7oBWY76FB4PpRxoQNI130 assertion
type: Assertion
description: [In contrast to the previously reported significant association between TAS2R16 and alcohol dependence, we found no evidence that TAS2R38 haplotypes influence alcohol dependence in the COGA dataset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17250611
was generated by: ECO_0000203

NP67570.RAX6mqYg0q4QdVs8suYXxaCxnxS NWugUfWutyBUgY36Q
has assertion: NP67570.RAX6mqYg0q4QdVs8suYXxaCxnxS NWugUfWutyBUgY36Q130 assertion
has provenance: NP67570.RAX6mqYg0q4QdVs8suYXxaCxnxS NWugUfWutyBUgY36Q130 provenance
has publication info: NP67570.RAX6mqYg0q4QdVs8suYXxaCxnxS NWugUfWutyBUgY36Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67570.RAX6mqYg0q4QdVs8suYXxaCxnxS NWugUfWutyBUgY36Q130 assertion
type: Assertion
description: [SNPs discovered to date are suitable for risk prediction while additional SNPs discovered in the future may identify more subjects at higher risk. Men identified as high risk by SNP-based testing may be targeted for PCa screening or chemoprevention. The clinical impact on improving the effectiveness of these interventions can be and should be assessed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20878950
was generated by: ECO_0000203

NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8
has assertion: NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130 assertion
has provenance: NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130 provenance
has publication info: NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130 assertion
type: Assertion
description: [We confirm recent reports that 8q24 variants identified to be associated with prostate cancer in men of European descent are also associated with prostate cancer in African Americans. Our report is the first to find evidence of association between SNPs near MSMB and prostate cancer in African Americans. Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4, a SNP that has been implicated to be independently associated, with respect to the widely reported SNP rs10993994 in the nearby gene MSMB, with prostate cancer in men of European descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20717903
was generated by: ECO_0000203

NP67573.RAbD1ZLCA7CYyh-Ny39zM3EKcz2m2AjtFydh9rMLgkepk
has assertion: NP67573.RAbD1ZLCA7CYyh-Ny39zM3EKcz2m2AjtFydh9rMLgkepk130 assertion
has provenance: NP67573.RAbD1ZLCA7CYyh-Ny39zM3EKcz2m2AjtFydh9rMLgkepk130 provenance
has publication info: NP67573.RAbD1ZLCA7CYyh-Ny39zM3EKcz2m2AjtFydh9rMLgkepk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67573.RAbD1ZLCA7CYyh-Ny39zM3EKcz2m2AjtFydh9rMLgkepk130 assertion
type: Assertion
description: [Number of prostate cancer risk alleles may identify possibly 'insignificant' 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/20590552
was generated by: ECO_0000203

NP67576.RAZEUQdFTCQ iXaNwdsDQ15zTWtFnonw15I5m8fww3VL8
has assertion: NP67576.RAZEUQdFTCQ iXaNwdsDQ15zTWtFnonw15I5m8fww3VL8130 assertion
has provenance: NP67576.RAZEUQdFTCQ iXaNwdsDQ15zTWtFnonw15I5m8fww3VL8130 provenance
has publication info: NP67576.RAZEUQdFTCQ iXaNwdsDQ15zTWtFnonw15I5m8fww3VL8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67576.RAZEUQdFTCQ iXaNwdsDQ15zTWtFnonw15I5m8fww3VL8130 assertion
type: Assertion
description: [rs1447295, rs6983561 and rs4430796 showed strong evidence of an association with prostate cancer after adjustments for 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/20026053
was generated by: ECO_0000203

NP67578.RAdx63GVXc2sOWm4P-DUIgizoe-QS0DihOgZmJsQjyCeA
has assertion: NP67578.RAdx63GVXc2sOWm4P-DUIgizoe-QS0DihOgZmJsQjyCeA130 assertion
has provenance: NP67578.RAdx63GVXc2sOWm4P-DUIgizoe-QS0DihOgZmJsQjyCeA130 provenance
has publication info: NP67578.RAdx63GVXc2sOWm4P-DUIgizoe-QS0DihOgZmJsQjyCeA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67578.RAdx63GVXc2sOWm4P-DUIgizoe-QS0DihOgZmJsQjyCeA130 assertion
type: Assertion
description: [We identified associations between prostate cancer susceptibility SNPs and clinical end points. The rs61752561 in KLK3 and rs2735839 in the KLK2-KLK3 intergenic region were strongly associated with prostate cancer-specific survival, and rs10486567 in the 7JAZF1 gene were associated with biochemical recurrence. A larger study will be required to independently validate these findings and determine the role of these SNPs in prognostic models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20460480
was generated by: ECO_0000203

NP67584.RAW82GTr-S3UPBXyG42Zh6-QmEPiQzqxhv9gSQixBX8DI
has assertion: NP67584.RAW82GTr-S3UPBXyG42Zh6-QmEPiQzqxhv9gSQixBX8DI130 assertion
has provenance: NP67584.RAW82GTr-S3UPBXyG42Zh6-QmEPiQzqxhv9gSQixBX8DI130 provenance
has publication info: NP67584.RAW82GTr-S3UPBXyG42Zh6-QmEPiQzqxhv9gSQixBX8DI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67584.RAW82GTr-S3UPBXyG42Zh6-QmEPiQzqxhv9gSQixBX8DI130 assertion
type: Assertion
description: [Transforming growth factor-beta1 polymorphisms in patients with brucellosis: an association between codon 10 and 25 polymorphisms and 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/17184296
was generated by: ECO_0000203

NP67585.RAQfLrOCFBJ-IVkdzXxJURyBasLFrIWnItJIDvlNBtIkc
has assertion: NP67585.RAQfLrOCFBJ-IVkdzXxJURyBasLFrIWnItJIDvlNBtIkc130 assertion
has provenance: NP67585.RAQfLrOCFBJ-IVkdzXxJURyBasLFrIWnItJIDvlNBtIkc130 provenance
has publication info: NP67585.RAQfLrOCFBJ-IVkdzXxJURyBasLFrIWnItJIDvlNBtIkc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67585.RAQfLrOCFBJ-IVkdzXxJURyBasLFrIWnItJIDvlNBtIkc130 assertion
type: Assertion
description: [Microsatelite GT polymorphism in the toll-like receptor 2 is associated 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/16879199
was generated by: ECO_0000203

NP67587.RAZzLq9cQTiD8KeoxWrQDrqnvjtHpKQb95JM3A7Po54Hw
has assertion: NP67587.RAZzLq9cQTiD8KeoxWrQDrqnvjtHpKQb95JM3A7Po54Hw130 assertion
has provenance: NP67587.RAZzLq9cQTiD8KeoxWrQDrqnvjtHpKQb95JM3A7Po54Hw130 provenance
has publication info: NP67587.RAZzLq9cQTiD8KeoxWrQDrqnvjtHpKQb95JM3A7Po54Hw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67587.RAZzLq9cQTiD8KeoxWrQDrqnvjtHpKQb95JM3A7Po54Hw130 assertion
type: Assertion
description: [-238 G>A polymorphism of tumor necrosis factor alpha gene (TNFA) is associated with alcoholic liver cirrhosis in alcoholic Spanish 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/16340448
was generated by: ECO_0000203

NP67588.RAfV4OyCF1BiDoI65oq9Qxt8-VbQ7UsV 11Dj44foEikI
has assertion: NP67588.RAfV4OyCF1BiDoI65oq9Qxt8-VbQ7UsV 11Dj44foEikI130 assertion
has provenance: NP67588.RAfV4OyCF1BiDoI65oq9Qxt8-VbQ7UsV 11Dj44foEikI130 provenance
has publication info: NP67588.RAfV4OyCF1BiDoI65oq9Qxt8-VbQ7UsV 11Dj44foEikI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67588.RAfV4OyCF1BiDoI65oq9Qxt8-VbQ7UsV 11Dj44foEikI130 assertion
type: Assertion
description: [Tumor necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta), produced by endotoxin-activated Kupffer cells, play a key role in the pathogenesis of alcoholic liver cirrhosis (ALC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19278365
was generated by: ECO_0000203

NP67594.RAX7GfGlYtmVavrEZZZkKYZpyEaLzWJMxHqw1z 8MCI4s
has assertion: NP67594.RAX7GfGlYtmVavrEZZZkKYZpyEaLzWJMxHqw1z 8MCI4s130 assertion
has provenance: NP67594.RAX7GfGlYtmVavrEZZZkKYZpyEaLzWJMxHqw1z 8MCI4s130 provenance
has publication info: NP67594.RAX7GfGlYtmVavrEZZZkKYZpyEaLzWJMxHqw1z 8MCI4s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67594.RAX7GfGlYtmVavrEZZZkKYZpyEaLzWJMxHqw1z 8MCI4s130 assertion
type: Assertion
description: [To investigate the effect of single nucleotide polymorphisms (SNPs) of the upstream stimulatory factor (USF) 1 and 2 genes on the onset of Alzheimer's disease (AD), a case-control study was performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16870626
was generated by: ECO_0000203

NP67596.RAVr4 ENFHUh6spOEUi0BEDXnU0XLio M2LvMxEVmmHZ8
has assertion: NP67596.RAVr4 ENFHUh6spOEUi0BEDXnU0XLio M2LvMxEVmmHZ8130 assertion
has provenance: NP67596.RAVr4 ENFHUh6spOEUi0BEDXnU0XLio M2LvMxEVmmHZ8130 provenance
has publication info: NP67596.RAVr4 ENFHUh6spOEUi0BEDXnU0XLio M2LvMxEVmmHZ8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67596.RAVr4 ENFHUh6spOEUi0BEDXnU0XLio M2LvMxEVmmHZ8130 assertion
type: Assertion
description: [Urotensin II gene may contribute to the genetic susceptibility to gestational diabetes mellitus in northern 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/17327028
was generated by: ECO_0000203

NP67602.RAbQvC8XKXv0IHawkoko9aGuHICjhjrU0zCEdemIK-Zfc
has assertion: NP67602.RAbQvC8XKXv0IHawkoko9aGuHICjhjrU0zCEdemIK-Zfc130 assertion
has provenance: NP67602.RAbQvC8XKXv0IHawkoko9aGuHICjhjrU0zCEdemIK-Zfc130 provenance
has publication info: NP67602.RAbQvC8XKXv0IHawkoko9aGuHICjhjrU0zCEdemIK-Zfc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67602.RAbQvC8XKXv0IHawkoko9aGuHICjhjrU0zCEdemIK-Zfc130 assertion
type: Assertion
description: [VEGF genetic variability is associated with increased risk of developing 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/19272614
was generated by: ECO_0000203

NP67604.RAUrIjgHmH3a4Nbh9HIQ1iEXynRzErFdyw644-66A2oww
has assertion: NP67604.RAUrIjgHmH3a4Nbh9HIQ1iEXynRzErFdyw644-66A2oww130 assertion
has provenance: NP67604.RAUrIjgHmH3a4Nbh9HIQ1iEXynRzErFdyw644-66A2oww130 provenance
has publication info: NP67604.RAUrIjgHmH3a4Nbh9HIQ1iEXynRzErFdyw644-66A2oww130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67604.RAUrIjgHmH3a4Nbh9HIQ1iEXynRzErFdyw644-66A2oww130 assertion
type: Assertion
description: [Recent evidences indicate that polymorphisms within the promoter region of the vascular endothelial growth factor (VEGF) gene may elevate the risk for 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/20138124
was generated by: ECO_0000203

NP67608.RASK2EOzNd6NXtRy7EZiDi2oaOEjEyByPCpvDKthKgW4I
has assertion: NP67608.RASK2EOzNd6NXtRy7EZiDi2oaOEjEyByPCpvDKthKgW4I130 assertion
has provenance: NP67608.RASK2EOzNd6NXtRy7EZiDi2oaOEjEyByPCpvDKthKgW4I130 provenance
has publication info: NP67608.RASK2EOzNd6NXtRy7EZiDi2oaOEjEyByPCpvDKthKgW4I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67608.RASK2EOzNd6NXtRy7EZiDi2oaOEjEyByPCpvDKthKgW4I130 assertion
type: Assertion
description: [Polymorphisms in the genes ERCC2, XRCC3 and CD3EAP influence treatment outcome in multiple myeloma patients undergoing autologous bone marrow 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/17131345
was generated by: ECO_0000203

NP67619.RAfwaKtXxxbwuz5-GK0EyFbFOGK0WeVAXW6jhdwchO9Gc
has assertion: NP67619.RAfwaKtXxxbwuz5-GK0EyFbFOGK0WeVAXW6jhdwchO9Gc130 assertion
has provenance: NP67619.RAfwaKtXxxbwuz5-GK0EyFbFOGK0WeVAXW6jhdwchO9Gc130 provenance
has publication info: NP67619.RAfwaKtXxxbwuz5-GK0EyFbFOGK0WeVAXW6jhdwchO9Gc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67619.RAfwaKtXxxbwuz5-GK0EyFbFOGK0WeVAXW6jhdwchO9Gc130 assertion
type: Assertion
description: [Previous studies in three independent cohorts have shown that the rs1858830 C allele variant in the promoter region of the MET gene on chromosome 7q31 is associated with autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19681062
was generated by: ECO_0000203

NP67622.RAZBOO0 gpFqzgiDeJ6eebCKpJ sP9G gzImatIzIN9jk
has assertion: NP67622.RAZBOO0 gpFqzgiDeJ6eebCKpJ sP9G gzImatIzIN9jk130 assertion
has provenance: NP67622.RAZBOO0 gpFqzgiDeJ6eebCKpJ sP9G gzImatIzIN9jk130 provenance
has publication info: NP67622.RAZBOO0 gpFqzgiDeJ6eebCKpJ sP9G gzImatIzIN9jk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67622.RAZBOO0 gpFqzgiDeJ6eebCKpJ sP9G gzImatIzIN9jk130 assertion
type: Assertion
description: [Mutations of hemochromatosis gene in volunteer blood donors and Chilean porphyria cutanea tarda 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/17137171
was generated by: ECO_0000203

NP67648.RAea3E8Uc1mr4L8K4TaoSO0loIZlMzYsXPqKkB47xKytc
has assertion: NP67648.RAea3E8Uc1mr4L8K4TaoSO0loIZlMzYsXPqKkB47xKytc130 assertion
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has publication info: NP67648.RAea3E8Uc1mr4L8K4TaoSO0loIZlMzYsXPqKkB47xKytc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67648.RAea3E8Uc1mr4L8K4TaoSO0loIZlMzYsXPqKkB47xKytc130 assertion
type: Assertion
description: [OAS1 gene haplotype confers susceptibility to 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/17092260
was generated by: ECO_0000203

NP67649.RAb5SIntKk8hqeMxk9JULUKl1xAwKTMvo1PzHu91Sjql0
has assertion: NP67649.RAb5SIntKk8hqeMxk9JULUKl1xAwKTMvo1PzHu91Sjql0130 assertion
has provenance: NP67649.RAb5SIntKk8hqeMxk9JULUKl1xAwKTMvo1PzHu91Sjql0130 provenance
has publication info: NP67649.RAb5SIntKk8hqeMxk9JULUKl1xAwKTMvo1PzHu91Sjql0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67649.RAb5SIntKk8hqeMxk9JULUKl1xAwKTMvo1PzHu91Sjql0130 assertion
type: Assertion
description: [A functional OAS1 SNP, AA genotype, confers susceptibility to MS and the GG genotype may protect against 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/20679634
was generated by: ECO_0000203

NP67651.RAQWGnetjTcgJ-l4UplnGI6v 4S7wigsNZ-oddkMnm3gw
has assertion: NP67651.RAQWGnetjTcgJ-l4UplnGI6v 4S7wigsNZ-oddkMnm3gw130 assertion
has provenance: NP67651.RAQWGnetjTcgJ-l4UplnGI6v 4S7wigsNZ-oddkMnm3gw130 provenance
has publication info: NP67651.RAQWGnetjTcgJ-l4UplnGI6v 4S7wigsNZ-oddkMnm3gw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67651.RAQWGnetjTcgJ-l4UplnGI6v 4S7wigsNZ-oddkMnm3gw130 assertion
type: Assertion
description: [Single nucleotide polymorphisms in miRNA binding sites and miRNA genes as breast/ovarian cancer risk modifiers in Jewish high-risk 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/19950226
was generated by: ECO_0000203

NP67658.RAayDJie-bXgNRFygtiv1rKJa-jdiK5aNPn pD51Tc5OQ
has assertion: NP67658.RAayDJie-bXgNRFygtiv1rKJa-jdiK5aNPn pD51Tc5OQ130 assertion
has provenance: NP67658.RAayDJie-bXgNRFygtiv1rKJa-jdiK5aNPn pD51Tc5OQ130 provenance
has publication info: NP67658.RAayDJie-bXgNRFygtiv1rKJa-jdiK5aNPn pD51Tc5OQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67658.RAayDJie-bXgNRFygtiv1rKJa-jdiK5aNPn pD51Tc5OQ130 assertion
type: Assertion
description: [We therefore investigated in a cohort of HIV-infected Tanzanian patients whether the Asp299Gly TLR4 polymorphism is associated with the development of active 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/17545720
was generated by: ECO_0000203

NP67669.RARlpfBz7U1j2J61lC625gyLAuuaOShF83wCVlPpdymf8
has assertion: NP67669.RARlpfBz7U1j2J61lC625gyLAuuaOShF83wCVlPpdymf8130 assertion
has provenance: NP67669.RARlpfBz7U1j2J61lC625gyLAuuaOShF83wCVlPpdymf8130 provenance
has publication info: NP67669.RARlpfBz7U1j2J61lC625gyLAuuaOShF83wCVlPpdymf8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67669.RARlpfBz7U1j2J61lC625gyLAuuaOShF83wCVlPpdymf8130 assertion
type: Assertion
description: [Our data suggest that cat but not dog ownership substantially increases the risk of eczema within the first year of life in children with FLG loss-of-function variants, but not amongst those without.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18578563
was generated by: ECO_0000203

NP67684.RAUQNaH5SUj9i9tVWgCpsy5QD5hKiSQinAfiXsEG0omrk
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP67684.RAUQNaH5SUj9i9tVWgCpsy5QD5hKiSQinAfiXsEG0omrk130 assertion
type: Assertion
description: [Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of 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/18628988
was generated by: ECO_0000203

NP67689.RAeHH2AMvR0XK7NkMwS9eyQi0HGPJuHJBfXpn18QKoXrk
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP67689.RAeHH2AMvR0XK7NkMwS9eyQi0HGPJuHJBfXpn18QKoXrk130 assertion
type: Assertion
description: [Genetic polymorphisms in nitric oxide synthase genes modify the relationship between vegetable and fruit intake and risk of 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/19423521
was generated by: ECO_0000203

NP67696.RAYH8nLXOxfdACt4sAc5ugf4JaUDf1IPEpN1A9FDr4PPg
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP67696.RAYH8nLXOxfdACt4sAc5ugf4JaUDf1IPEpN1A9FDr4PPg130 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

NP67698.RAUsXkdW4HFaKVBfS7EA-kUkqfehnmCvR9ATV2yhNysQg
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP67698.RAUsXkdW4HFaKVBfS7EA-kUkqfehnmCvR9ATV2yhNysQg130 assertion
type: Assertion
description: [Examination of tetrahydrobiopterin pathway genes in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19674121
was generated by: ECO_0000203

NP67700.RAaIqTVBo-3BwN1d0f0Yz3qwqmJ VDz-cOvq5oOVUmrdo
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP67700.RAaIqTVBo-3BwN1d0f0Yz3qwqmJ VDz-cOvq5oOVUmrdo130 assertion
type: Assertion
description: [Transcriptomic and genetic studies identify IL-33 as a candidate gene 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/19204726
was generated by: ECO_0000203

NP67702.RAdfCFWh8uZmHgsMa-RMSM068S3rgmszZ5ch4xP4sTc8E
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP67702.RAdfCFWh8uZmHgsMa-RMSM068S3rgmszZ5ch4xP4sTc8E130 assertion
type: Assertion
description: [Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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SIO_000772: http://identifiers.org/pubmed/19913121
was generated by: ECO_0000203

NP67704.RARrdP1-oWA--vfY00gQbFxjVHknjaO5QKB908jj4sK1s
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP67704.RARrdP1-oWA--vfY00gQbFxjVHknjaO5QKB908jj4sK1s130 assertion
type: Assertion
description: [A genome-wide association study for late-onset Alzheimer's disease using DNA pooling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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SIO_000772: http://identifiers.org/pubmed/18823527
was generated by: ECO_0000203

NP67706.RAV LXKGoeRVeh1DX3OSuzb2B1TEY2kaxq2iMHiA4bNCU
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP67706.RAV LXKGoeRVeh1DX3OSuzb2B1TEY2kaxq2iMHiA4bNCU130 assertion
type: Assertion
description: [Genome-wide association analysis of age-at-onset 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/22005931
was generated by: ECO_0000203

NP67708.RASU26rbRP1YIh9uNU0gLVMVrvYpy9VUuSTv1DfBODKtM
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP67708.RASU26rbRP1YIh9uNU0gLVMVrvYpy9VUuSTv1DfBODKtM130 assertion
type: Assertion
description: [Genetic variation in GHRL may have a modest impact on BMI in European 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/19077438
was generated by: ECO_0000203

NP67716.RAaNZG5aoo68YXabmRnGxzwRcMl kmKV2U9BUlFHz5vCY
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP67716.RAaNZG5aoo68YXabmRnGxzwRcMl kmKV2U9BUlFHz5vCY130 assertion
type: Assertion
description: [Genetic mutations associated with cigarette smoking 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/19351817
was generated by: ECO_0000203

NP67721.RAWEMjJxBGTGGpOsiJTCIFchq84TDr29Xeouj8 SuCCzY
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP67721.RAWEMjJxBGTGGpOsiJTCIFchq84TDr29Xeouj8 SuCCzY130 assertion
type: Assertion
description: [These results support polygenic genetics for success in abstaining from smoking, overlap with genetics of substance dependence and memory, and nominate gene variants for selective influences on therapeutic responses to bupropion vs NRT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18519826
was generated by: ECO_0000203

NP67725.RAXG7rbyweGLik34WWhYt6AgRC6rz6n85NVdQq2TGU2iQ
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP67725.RAXG7rbyweGLik34WWhYt6AgRC6rz6n85NVdQq2TGU2iQ130 assertion
type: Assertion
description: [A regulatory polymorphism at position -309 in PTPRCAP is associated with susceptibility to diffuse-type gastric cancer and gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20019842
was generated by: ECO_0000203

NP67726.RATdGBQNuq6BvucBRKzo4NMtx9mxPA59kZDv9IZlqphbo
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP67726.RATdGBQNuq6BvucBRKzo4NMtx9mxPA59kZDv9IZlqphbo130 assertion
type: Assertion
description: [Genetic variation in GHRL may have a modest impact on BMI in European 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/19077438
was generated by: ECO_0000203

NP67727.RAWMYGU8n2F8NWSQnsauF-zjkOBPrFg2gbwahu7O6xl1k
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP67727.RAWMYGU8n2F8NWSQnsauF-zjkOBPrFg2gbwahu7O6xl1k130 assertion
type: Assertion
description: [Transcriptomic and genetic studies identify IL-33 as a candidate gene 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/19204726
was generated by: ECO_0000203

NP67728.RAffdXd5sJpHMZhiABYrfsPR1sMeg72cWKMe-lrYS9W8Y
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP67728.RAffdXd5sJpHMZhiABYrfsPR1sMeg72cWKMe-lrYS9W8Y130 assertion
type: Assertion
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SIO_000772: http://identifiers.org/pubmed/18375974
was generated by: ECO_0000203

NP67734.RAZdoEBHo22x97ziyVaokI6MOiG2tR3AJs6PB8XmzcYys
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67734.RAZdoEBHo22x97ziyVaokI6MOiG2tR3AJs6PB8XmzcYys130 assertion
type: Assertion
description: [Genome-wide association defines more than 30 distinct susceptibility loci for 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/18587394
was generated by: ECO_0000203

NP67741.RAS7EXfXzzos0GgDreTWJVmQcIpQH5fQWs5g1htv6y1Bc
has assertion: NP67741.RAS7EXfXzzos0GgDreTWJVmQcIpQH5fQWs5g1htv6y1Bc130 assertion
has provenance: NP67741.RAS7EXfXzzos0GgDreTWJVmQcIpQH5fQWs5g1htv6y1Bc130 provenance
has publication info: NP67741.RAS7EXfXzzos0GgDreTWJVmQcIpQH5fQWs5g1htv6y1Bc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67741.RAS7EXfXzzos0GgDreTWJVmQcIpQH5fQWs5g1htv6y1Bc130 assertion
type: Assertion
description: [Allele and haplotype frequency distribution in PTPN22 gene across variable ethnic groups: Implications for genetic association studies for 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/20166877
was generated by: ECO_0000203

NP67748.RAYo2HBcsTHUL5sFrOs lbnV5SgJ26-LN2WbPuwkxMVQE
has assertion: NP67748.RAYo2HBcsTHUL5sFrOs lbnV5SgJ26-LN2WbPuwkxMVQE130 assertion
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has publication info: NP67748.RAYo2HBcsTHUL5sFrOs lbnV5SgJ26-LN2WbPuwkxMVQE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP67748.RAYo2HBcsTHUL5sFrOs lbnV5SgJ26-LN2WbPuwkxMVQE130 assertion
type: Assertion
description: [These results support polygenic genetics for success in abstaining from smoking, overlap with genetics of substance dependence and memory, and nominate gene variants for selective influences on therapeutic responses to bupropion vs NRT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18519826
was generated by: ECO_0000203

NP67756.RAbxnRtn5uTmRuhURhLklRUa wI4H7Sm4mIrW39GFUUVk
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP67756.RAbxnRtn5uTmRuhURhLklRUa wI4H7Sm4mIrW39GFUUVk130 assertion
type: Assertion
description: [Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic 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/17910045
was generated by: ECO_0000203

NP67770.RASyQVaq1Dd4H6Y28DdlqCmzism-8QXvQ-M4x3Yg56-A0
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP67770.RASyQVaq1Dd4H6Y28DdlqCmzism-8QXvQ-M4x3Yg56-A0130 assertion
type: Assertion
description: [Functional polymorphisms of the cyclooxygenase (PTGS2) gene and risk for gallbladder cancer in a North Indian 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/19455278
was generated by: ECO_0000203

NP67772.RAb7hlvd6kjoTs4ZDFx4qkplBwWHi3B8tFDTIsi6dxslo
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP67772.RAb7hlvd6kjoTs4ZDFx4qkplBwWHi3B8tFDTIsi6dxslo130 assertion
type: Assertion
description: [Collectively, these findings confirm that the COX-2 -765G>C polymorphism is a risk factor for the development of bladder cancer and can provide a plausible mechanistic explanation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20627335
was generated by: ECO_0000203

NP67773.RAcdApv0lJHiqoZGS1QooQUGR8hmX1oMXaWQEZmmwX4Yw
has assertion: NP67773.RAcdApv0lJHiqoZGS1QooQUGR8hmX1oMXaWQEZmmwX4Yw130 assertion
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has publication info: NP67773.RAcdApv0lJHiqoZGS1QooQUGR8hmX1oMXaWQEZmmwX4Yw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP67773.RAcdApv0lJHiqoZGS1QooQUGR8hmX1oMXaWQEZmmwX4Yw130 assertion
type: Assertion
description: [Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18471798
was generated by: ECO_0000203

NP67775.RAZ-PxuhKWV6PmAGLdWMJiUy1lTUsO5EmLZgEDyhIbq2o
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has publication info: NP67775.RAZ-PxuhKWV6PmAGLdWMJiUy1lTUsO5EmLZgEDyhIbq2o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP67775.RAZ-PxuhKWV6PmAGLdWMJiUy1lTUsO5EmLZgEDyhIbq2o130 assertion
type: Assertion
description: [This study evaluated the relationship between autism spectrum disorders (ASDs) and polymorphisms of PTGS2 (the gene encoding Cox-2) with 151 Korean family trios including children with ASDs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18579107
was generated by: ECO_0000203

NP67777.RARcmYcijZ3oG FKbVNmXg5EMUiaQ0l6-uyFhx5LUe98o
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has publication info: NP67777.RARcmYcijZ3oG FKbVNmXg5EMUiaQ0l6-uyFhx5LUe98o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP67777.RARcmYcijZ3oG FKbVNmXg5EMUiaQ0l6-uyFhx5LUe98o130 assertion
type: Assertion
description: [COX2 and p53 risk-alleles coexist in COPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18692035
was generated by: ECO_0000203

NP67779.RATXDKznucJaDZheLcLRJwyDo0cym056g5Rd1Q4zmTGzc
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP67779.RATXDKznucJaDZheLcLRJwyDo0cym056g5Rd1Q4zmTGzc130 assertion
type: Assertion
description: [For the first time, we provide evidence that functional polymorphisms in the COX2 gene may influence the risk of vitiligo in Han Chinese populations, suggesting new clues that help to clarify the pathogenesis of vitiligo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19004621
was generated by: ECO_0000203

NP67780.RAVCOCy0ReapdBncHwH0aT66tYgvV9H0F8mqVFuVW15uI
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67780.RAVCOCy0ReapdBncHwH0aT66tYgvV9H0F8mqVFuVW15uI130 assertion
type: Assertion
description: [Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21085187
was generated by: ECO_0000203

NP67782.RAQSukdylopEj-Ttm4UYfFSNZWUAvN7nPPu51VwhXfftA
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67782.RAQSukdylopEj-Ttm4UYfFSNZWUAvN7nPPu51VwhXfftA130 assertion
type: Assertion
description: [Our data suggest that the homozygous CC genotype of the COX2.8473 T > C polymorphism may be associated with sarcoidosis 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/19042116
was generated by: ECO_0000203

NP67783.RAUlxRJ9g97lfAqEIMA5jx2kqgrs18CuVM6I1AmzMJeIU
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67783.RAUlxRJ9g97lfAqEIMA5jx2kqgrs18CuVM6I1AmzMJeIU130 assertion
type: Assertion
description: [Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic 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/19056482
was generated by: ECO_0000203

NP67787.RAQMB9QpG-VszqDo3LrhrT5OMa7Z3vmqsI4Emg0MqHllo
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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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

NP67787.RAQMB9QpG-VszqDo3LrhrT5OMa7Z3vmqsI4Emg0MqHllo130 assertion
type: Assertion
description: [Our results confirm the protective effect of NSAID use on 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/19075598
was generated by: ECO_0000203

NP67788.RATvwbi7-fm2bqCb1Iy8weekZ68ap3CgKW3fAvGXGqJOk
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP67788.RATvwbi7-fm2bqCb1Iy8weekZ68ap3CgKW3fAvGXGqJOk130 assertion
type: Assertion
description: [The genomic basis of cerebral palsy: a HuGE systematic literature 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/19238444
was generated by: ECO_0000203

NP67792.RARs0rdlCOOD8pGXzw IWHhzQV9PBuBOXPw2xj27 y9zk
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67792.RARs0rdlCOOD8pGXzw IWHhzQV9PBuBOXPw2xj27 y9zk130 assertion
type: Assertion
description: [G-765C COX-2 gene promoter polymorphism and risk of atherosclerosis after kidney 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/19920789
was generated by: ECO_0000203

NP67796.RAeJCvvGLEBHXYQBEFN 5MaMVtpBdh9J3XhoHEHflAocg
has assertion: NP67796.RAeJCvvGLEBHXYQBEFN 5MaMVtpBdh9J3XhoHEHflAocg130 assertion
has provenance: NP67796.RAeJCvvGLEBHXYQBEFN 5MaMVtpBdh9J3XhoHEHflAocg130 provenance
has publication info: NP67796.RAeJCvvGLEBHXYQBEFN 5MaMVtpBdh9J3XhoHEHflAocg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67796.RAeJCvvGLEBHXYQBEFN 5MaMVtpBdh9J3XhoHEHflAocg130 assertion
type: Assertion
description: [Participants with the PLA2 BanI GG or the COX2 rs4648308 AG genotypes had a higher risk of IFN-alpha-induced depression (odds ratio = 3.1 and 3.5, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20034614
was generated by: ECO_0000203

NP67802.RATzDTk6PcCcXWqwNY4Ys5kOQ0VxhevN3xOoNSpy0x51s
has assertion: NP67802.RATzDTk6PcCcXWqwNY4Ys5kOQ0VxhevN3xOoNSpy0x51s130 assertion
has provenance: NP67802.RATzDTk6PcCcXWqwNY4Ys5kOQ0VxhevN3xOoNSpy0x51s130 provenance
has publication info: NP67802.RATzDTk6PcCcXWqwNY4Ys5kOQ0VxhevN3xOoNSpy0x51s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67802.RATzDTk6PcCcXWqwNY4Ys5kOQ0VxhevN3xOoNSpy0x51s130 assertion
type: Assertion
description: [Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white 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/19064572
was generated by: ECO_0000203

NP67803.RAbroCXqGJmN0gh9--PaYcYGcPP-zAfuR6HB4TggGfoC8
has assertion: NP67803.RAbroCXqGJmN0gh9--PaYcYGcPP-zAfuR6HB4TggGfoC8130 assertion
has provenance: NP67803.RAbroCXqGJmN0gh9--PaYcYGcPP-zAfuR6HB4TggGfoC8130 provenance
has publication info: NP67803.RAbroCXqGJmN0gh9--PaYcYGcPP-zAfuR6HB4TggGfoC8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67803.RAbroCXqGJmN0gh9--PaYcYGcPP-zAfuR6HB4TggGfoC8130 assertion
type: Assertion
description: [Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic 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/19056482
was generated by: ECO_0000203

NP67805.RAe h02xxgwt R7DNMxm2KXNb6ec4BB8RGW49h1ioWwy8
has assertion: NP67805.RAe h02xxgwt R7DNMxm2KXNb6ec4BB8RGW49h1ioWwy8130 assertion
has provenance: NP67805.RAe h02xxgwt R7DNMxm2KXNb6ec4BB8RGW49h1ioWwy8130 provenance
has publication info: NP67805.RAe h02xxgwt R7DNMxm2KXNb6ec4BB8RGW49h1ioWwy8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67805.RAe h02xxgwt R7DNMxm2KXNb6ec4BB8RGW49h1ioWwy8130 assertion
type: Assertion
description: [Specific PTGIS and TBXAS1 variants may affect breast cancer susceptibility, but common variants in PTGS1, PTGS2, PTGES, PTGDS, and PGDS have no major role in breast 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/19276290
was generated by: ECO_0000203

NP67808.RAS87jfjeR7lsHGUc7mkCmEEOEX-Q7xk1vW61TG1uzG00
has assertion: NP67808.RAS87jfjeR7lsHGUc7mkCmEEOEX-Q7xk1vW61TG1uzG00130 assertion
has provenance: NP67808.RAS87jfjeR7lsHGUc7mkCmEEOEX-Q7xk1vW61TG1uzG00130 provenance
has publication info: NP67808.RAS87jfjeR7lsHGUc7mkCmEEOEX-Q7xk1vW61TG1uzG00130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67808.RAS87jfjeR7lsHGUc7mkCmEEOEX-Q7xk1vW61TG1uzG00130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP67810.RAd6hKFIgY5CiXtSR ERCwd9gOaqDiJXqtyEa8LEU1WTg
has assertion: NP67810.RAd6hKFIgY5CiXtSR ERCwd9gOaqDiJXqtyEa8LEU1WTg130 assertion
has provenance: NP67810.RAd6hKFIgY5CiXtSR ERCwd9gOaqDiJXqtyEa8LEU1WTg130 provenance
has publication info: NP67810.RAd6hKFIgY5CiXtSR ERCwd9gOaqDiJXqtyEa8LEU1WTg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67810.RAd6hKFIgY5CiXtSR ERCwd9gOaqDiJXqtyEa8LEU1WTg130 assertion
type: Assertion
description: [The presence of the GP VI 13254C allele is an independent predictor of 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/19786296
was generated by: ECO_0000203

NP67815.RAcnhpkkXPtpQo9ozlyrIIBbgnvM9OJrFcSn5EasfnIPc
has assertion: NP67815.RAcnhpkkXPtpQo9ozlyrIIBbgnvM9OJrFcSn5EasfnIPc130 assertion
has provenance: NP67815.RAcnhpkkXPtpQo9ozlyrIIBbgnvM9OJrFcSn5EasfnIPc130 provenance
has publication info: NP67815.RAcnhpkkXPtpQo9ozlyrIIBbgnvM9OJrFcSn5EasfnIPc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67815.RAcnhpkkXPtpQo9ozlyrIIBbgnvM9OJrFcSn5EasfnIPc130 assertion
type: Assertion
description: [Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic 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/19056482
was generated by: ECO_0000203

NP67837.RAYKHLdVty74FSAyusWz0Pr6ueZzE4 2Qk084Jw49iU2g
has assertion: NP67837.RAYKHLdVty74FSAyusWz0Pr6ueZzE4 2Qk084Jw49iU2g130 assertion
has provenance: NP67837.RAYKHLdVty74FSAyusWz0Pr6ueZzE4 2Qk084Jw49iU2g130 provenance
has publication info: NP67837.RAYKHLdVty74FSAyusWz0Pr6ueZzE4 2Qk084Jw49iU2g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67837.RAYKHLdVty74FSAyusWz0Pr6ueZzE4 2Qk084Jw49iU2g130 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

NP67842.RAT1YM61CokioEPjDHOOfqfOjZk5jcBpb4iJG8BzBvc o
has assertion: NP67842.RAT1YM61CokioEPjDHOOfqfOjZk5jcBpb4iJG8BzBvc o130 assertion
has provenance: NP67842.RAT1YM61CokioEPjDHOOfqfOjZk5jcBpb4iJG8BzBvc o130 provenance
has publication info: NP67842.RAT1YM61CokioEPjDHOOfqfOjZk5jcBpb4iJG8BzBvc o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67842.RAT1YM61CokioEPjDHOOfqfOjZk5jcBpb4iJG8BzBvc o130 assertion
type: Assertion
description: [Analysis of candidate genes in occurrence and growth of colorectal adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19888426
was generated by: ECO_0000203

NP67844.RAQntXPQcWLLL1yVRZ0C05NoCLqlA0CcA8B-S1RwxKcMs
has assertion: NP67844.RAQntXPQcWLLL1yVRZ0C05NoCLqlA0CcA8B-S1RwxKcMs130 assertion
has provenance: NP67844.RAQntXPQcWLLL1yVRZ0C05NoCLqlA0CcA8B-S1RwxKcMs130 provenance
has publication info: NP67844.RAQntXPQcWLLL1yVRZ0C05NoCLqlA0CcA8B-S1RwxKcMs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67844.RAQntXPQcWLLL1yVRZ0C05NoCLqlA0CcA8B-S1RwxKcMs130 assertion
type: Assertion
description: [PTEN mutations and relationship to EGFR, ERBB2, KRAS, and TP53 mutations in non-small cell lung cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20018398
was generated by: ECO_0000203

NP67845.RAVpYkCZxUSxpCoKr262DjDMpjN56KCptxcNsG7yRJKG8
has assertion: NP67845.RAVpYkCZxUSxpCoKr262DjDMpjN56KCptxcNsG7yRJKG8130 assertion
has provenance: NP67845.RAVpYkCZxUSxpCoKr262DjDMpjN56KCptxcNsG7yRJKG8130 provenance
has publication info: NP67845.RAVpYkCZxUSxpCoKr262DjDMpjN56KCptxcNsG7yRJKG8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67845.RAVpYkCZxUSxpCoKr262DjDMpjN56KCptxcNsG7yRJKG8130 assertion
type: Assertion
description: [PI3K/PTEN/AKT/mTOR pathway genetic variation predicts toxicity and distant progression in lung cancer patients receiving platinum-based chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20447721
was generated by: ECO_0000203

NP67846.RASFuzDexLox3umTyCqyna0kWkkzM2q kikjtArdxN5QA
has assertion: NP67846.RASFuzDexLox3umTyCqyna0kWkkzM2q kikjtArdxN5QA130 assertion
has provenance: NP67846.RASFuzDexLox3umTyCqyna0kWkkzM2q kikjtArdxN5QA130 provenance
has publication info: NP67846.RASFuzDexLox3umTyCqyna0kWkkzM2q kikjtArdxN5QA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67846.RASFuzDexLox3umTyCqyna0kWkkzM2q kikjtArdxN5QA130 assertion
type: Assertion
description: [Our study demonstrates that mutations in each part of the EGFR pathway were associated with different clinicopathologic features in patients with NSCLCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20881644
was generated by: ECO_0000203

NP67847.RASuhCCKzM T g8NFfJmAtsQ0vWgZcI3U7ztvxUBAnnE4
has assertion: NP67847.RASuhCCKzM T g8NFfJmAtsQ0vWgZcI3U7ztvxUBAnnE4130 assertion
has provenance: NP67847.RASuhCCKzM T g8NFfJmAtsQ0vWgZcI3U7ztvxUBAnnE4130 provenance
has publication info: NP67847.RASuhCCKzM T g8NFfJmAtsQ0vWgZcI3U7ztvxUBAnnE4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67847.RASuhCCKzM T g8NFfJmAtsQ0vWgZcI3U7ztvxUBAnnE4130 assertion
type: Assertion
description: [Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white 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/19064572
was generated by: ECO_0000203

NP67852.RASvSjCyJ M0KNVjRnpAbUYIgevm AaMcXGd1q6uGG0F0
has assertion: NP67852.RASvSjCyJ M0KNVjRnpAbUYIgevm AaMcXGd1q6uGG0F0130 assertion
has provenance: NP67852.RASvSjCyJ M0KNVjRnpAbUYIgevm AaMcXGd1q6uGG0F0130 provenance
has publication info: NP67852.RASvSjCyJ M0KNVjRnpAbUYIgevm AaMcXGd1q6uGG0F0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67852.RASvSjCyJ M0KNVjRnpAbUYIgevm AaMcXGd1q6uGG0F0130 assertion
type: Assertion
description: [We show significant association between ERG gene rearrangements and PTEN genomic aberrations in subset of PCA. Our analysis also provides further support for the observation that homozygous PTEN deletions can occur within the subset of HGPIN lesions, and shows accumulating genetic aberrations with disease progression, evidenced by higher detection in PCA than in HGPIN and more PTEN homozygous deletions in GS 8-10 than in 6-7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20590547
was generated by: ECO_0000203

NP67854.RAbAMmQMf8EjmGlIxyQ22dRFLTHP94OvOhjqZGWf5WZh0
has assertion: NP67854.RAbAMmQMf8EjmGlIxyQ22dRFLTHP94OvOhjqZGWf5WZh0130 assertion
has provenance: NP67854.RAbAMmQMf8EjmGlIxyQ22dRFLTHP94OvOhjqZGWf5WZh0130 provenance
has publication info: NP67854.RAbAMmQMf8EjmGlIxyQ22dRFLTHP94OvOhjqZGWf5WZh0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67854.RAbAMmQMf8EjmGlIxyQ22dRFLTHP94OvOhjqZGWf5WZh0130 assertion
type: Assertion
description: [Concomitant PI3K-AKT and p53 alterations in endometrial carcinomas are associated with 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/19234438
was generated by: ECO_0000203

NP67866.RAf3UG0deuQzXJv3Z8ReaxTj3fQ2Am8Yxrz0Ji80 BmdY
has assertion: NP67866.RAf3UG0deuQzXJv3Z8ReaxTj3fQ2Am8Yxrz0Ji80 BmdY130 assertion
has provenance: NP67866.RAf3UG0deuQzXJv3Z8ReaxTj3fQ2Am8Yxrz0Ji80 BmdY130 provenance
has publication info: NP67866.RAf3UG0deuQzXJv3Z8ReaxTj3fQ2Am8Yxrz0Ji80 BmdY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67866.RAf3UG0deuQzXJv3Z8ReaxTj3fQ2Am8Yxrz0Ji80 BmdY130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP67867.RAZmWM3DYV1lO2K09DhPJDe1UY1UstHe tHyJpoLXuDmA
has assertion: NP67867.RAZmWM3DYV1lO2K09DhPJDe1UY1UstHe tHyJpoLXuDmA130 assertion
has provenance: NP67867.RAZmWM3DYV1lO2K09DhPJDe1UY1UstHe tHyJpoLXuDmA130 provenance
has publication info: NP67867.RAZmWM3DYV1lO2K09DhPJDe1UY1UstHe tHyJpoLXuDmA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67867.RAZmWM3DYV1lO2K09DhPJDe1UY1UstHe tHyJpoLXuDmA130 assertion
type: Assertion
description: [TAS2R38 polymorphisms are an important factor in determining ND in AAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18524836
was generated by: ECO_0000203

NP67872.RAQ-cXOFKd3fSutU1d7AUn1fooC0skrU64oosCC22-ZUU
has assertion: NP67872.RAQ-cXOFKd3fSutU1d7AUn1fooC0skrU64oosCC22-ZUU130 assertion
has provenance: NP67872.RAQ-cXOFKd3fSutU1d7AUn1fooC0skrU64oosCC22-ZUU130 provenance
has publication info: NP67872.RAQ-cXOFKd3fSutU1d7AUn1fooC0skrU64oosCC22-ZUU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67872.RAQ-cXOFKd3fSutU1d7AUn1fooC0skrU64oosCC22-ZUU130 assertion
type: Assertion
description: [Polymorphisms in inflammation-related genes are associated with susceptibility to major depression and antidepressant response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18504423
was generated by: ECO_0000203

NP67873.RASgUk11cureQby6 cwo2vTp496CQazEEqOWjVANiBDgE
has assertion: NP67873.RASgUk11cureQby6 cwo2vTp496CQazEEqOWjVANiBDgE130 assertion
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has publication info: NP67873.RASgUk11cureQby6 cwo2vTp496CQazEEqOWjVANiBDgE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67873.RASgUk11cureQby6 cwo2vTp496CQazEEqOWjVANiBDgE130 assertion
type: Assertion
description: [Polymorphisms in the genes encoding the 4 RET ligands, GDNF, NTN, ARTN, PSPN, and susceptibility to Hirschsprung 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/18970938
was generated by: ECO_0000203

NP67874.RAck0QxxeN-v6GgMMmLhGeF5tFiMdSMoPmRLRyOSbZOa8
has assertion: NP67874.RAck0QxxeN-v6GgMMmLhGeF5tFiMdSMoPmRLRyOSbZOa8130 assertion
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has publication info: NP67874.RAck0QxxeN-v6GgMMmLhGeF5tFiMdSMoPmRLRyOSbZOa8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67874.RAck0QxxeN-v6GgMMmLhGeF5tFiMdSMoPmRLRyOSbZOa8130 assertion
type: Assertion
description: [Single nucleotide polymorphisms in antigen processing machinery component ERAP1 significantly associate with clinical outcome in cervical 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/19202550
was generated by: ECO_0000203

NP67876.RAbeynVDEEwQFlGDa6MzxZMv1kPJQoZzKgLrmy3n7ZWc8
has assertion: NP67876.RAbeynVDEEwQFlGDa6MzxZMv1kPJQoZzKgLrmy3n7ZWc8130 assertion
has provenance: NP67876.RAbeynVDEEwQFlGDa6MzxZMv1kPJQoZzKgLrmy3n7ZWc8130 provenance
has publication info: NP67876.RAbeynVDEEwQFlGDa6MzxZMv1kPJQoZzKgLrmy3n7ZWc8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67876.RAbeynVDEEwQFlGDa6MzxZMv1kPJQoZzKgLrmy3n7ZWc8130 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

NP67878.RARWV7xep9bf96Ygv7hqDQJiQkaHOcCn-kOWRcKNeILyM
has assertion: NP67878.RARWV7xep9bf96Ygv7hqDQJiQkaHOcCn-kOWRcKNeILyM130 assertion
has provenance: NP67878.RARWV7xep9bf96Ygv7hqDQJiQkaHOcCn-kOWRcKNeILyM130 provenance
has publication info: NP67878.RARWV7xep9bf96Ygv7hqDQJiQkaHOcCn-kOWRcKNeILyM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67878.RARWV7xep9bf96Ygv7hqDQJiQkaHOcCn-kOWRcKNeILyM130 assertion
type: Assertion
description: [Single nucleotide polymorphisms in antigen processing machinery component ERAP1 significantly associate with clinical outcome in cervical 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/19202550
was generated by: ECO_0000203

NP67880.RAXF1abh48gbCOkqjLkm0gesD2KmRWN2JvqzLMHFk7UrU
has assertion: NP67880.RAXF1abh48gbCOkqjLkm0gesD2KmRWN2JvqzLMHFk7UrU130 assertion
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has publication info: NP67880.RAXF1abh48gbCOkqjLkm0gesD2KmRWN2JvqzLMHFk7UrU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67880.RAXF1abh48gbCOkqjLkm0gesD2KmRWN2JvqzLMHFk7UrU130 assertion
type: Assertion
description: [Large multifunctional protease LMP2 (Arg60-->His), LMP7 (Lys145-->Gln) and PSMA6 (C(-8)-->G) gene allelic polymorphisms in 147 young patients with essential hypertension and in 208 practically healthy people were determinated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19526842
was generated by: ECO_0000203

NP67882.RAeIkiVmV ndkPCxwrszqZCywHbe-N-n4Y1EM6mdzQiD8
has assertion: NP67882.RAeIkiVmV ndkPCxwrszqZCywHbe-N-n4Y1EM6mdzQiD8130 assertion
has provenance: NP67882.RAeIkiVmV ndkPCxwrszqZCywHbe-N-n4Y1EM6mdzQiD8130 provenance
has publication info: NP67882.RAeIkiVmV ndkPCxwrszqZCywHbe-N-n4Y1EM6mdzQiD8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67882.RAeIkiVmV ndkPCxwrszqZCywHbe-N-n4Y1EM6mdzQiD8130 assertion
type: Assertion
description: [Our results indicate that the PSMA6 variant rs1048990 is a risk factor of myocardial infarction in the 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/19272601
was generated by: ECO_0000203

NP67886.RAfgjOaDgRgF x9ea7- JuMDqGGixagw5zS4Ed4vCQouU
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has publication info: NP67886.RAfgjOaDgRgF x9ea7- JuMDqGGixagw5zS4Ed4vCQouU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67886.RAfgjOaDgRgF x9ea7- JuMDqGGixagw5zS4Ed4vCQouU130 assertion
type: Assertion
description: [Haplotype and cell proliferation analyses of candidate lung cancer susceptibility genes on chromosome 15q24-25.1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19789337
was generated by: ECO_0000203

NP67889.RAW9DDr5m5iCE70RdiccYqczFXRrBpL0M1sd4AOKsUvbY
has assertion: NP67889.RAW9DDr5m5iCE70RdiccYqczFXRrBpL0M1sd4AOKsUvbY130 assertion
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has publication info: NP67889.RAW9DDr5m5iCE70RdiccYqczFXRrBpL0M1sd4AOKsUvbY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67889.RAW9DDr5m5iCE70RdiccYqczFXRrBpL0M1sd4AOKsUvbY130 assertion
type: Assertion
description: [Several genome-wide association studies identified the chr15q25.1 region, which includes three nicotinic cholinergic receptor genes (CHRNA5-B4) and the cell proliferation gene (PSMA4), for its association with lung cancer risk in 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/20587604
was generated by: ECO_0000203

NP67898.RAWssAMYaPv1P8Jj9QaJzok9sg2KnGiVTWdQ05iID-Pd8
has assertion: NP67898.RAWssAMYaPv1P8Jj9QaJzok9sg2KnGiVTWdQ05iID-Pd8130 assertion
has provenance: NP67898.RAWssAMYaPv1P8Jj9QaJzok9sg2KnGiVTWdQ05iID-Pd8130 provenance
has publication info: NP67898.RAWssAMYaPv1P8Jj9QaJzok9sg2KnGiVTWdQ05iID-Pd8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67898.RAWssAMYaPv1P8Jj9QaJzok9sg2KnGiVTWdQ05iID-Pd8130 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

NP67905.RAVylQgtrzXMsFhICzYq5Gjk4MecBvzLCwIunnGbOdKKk
has assertion: NP67905.RAVylQgtrzXMsFhICzYq5Gjk4MecBvzLCwIunnGbOdKKk130 assertion
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has publication info: NP67905.RAVylQgtrzXMsFhICzYq5Gjk4MecBvzLCwIunnGbOdKKk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67905.RAVylQgtrzXMsFhICzYq5Gjk4MecBvzLCwIunnGbOdKKk130 assertion
type: Assertion
description: [Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary 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/19648920
was generated by: ECO_0000203

NP67908.RAU8lE2FnZkhruwZMel0XmV-W5b N9NkA9FPzBwVNqX3s
has assertion: NP67908.RAU8lE2FnZkhruwZMel0XmV-W5b N9NkA9FPzBwVNqX3s130 assertion
has provenance: NP67908.RAU8lE2FnZkhruwZMel0XmV-W5b N9NkA9FPzBwVNqX3s130 provenance
has publication info: NP67908.RAU8lE2FnZkhruwZMel0XmV-W5b N9NkA9FPzBwVNqX3s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67908.RAU8lE2FnZkhruwZMel0XmV-W5b N9NkA9FPzBwVNqX3s130 assertion
type: Assertion
description: [Genetic variation of PSCA gene is associated with the risk of both diffuse- and intestinal-type gastric cancer 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/20131315
was generated by: ECO_0000203

NP67915.RARsRbYm4cMe1Iyg JJycDAdwrCaIDe6SnxWIAYDuIwTI
has assertion: NP67915.RARsRbYm4cMe1Iyg JJycDAdwrCaIDe6SnxWIAYDuIwTI130 assertion
has provenance: NP67915.RARsRbYm4cMe1Iyg JJycDAdwrCaIDe6SnxWIAYDuIwTI130 provenance
has publication info: NP67915.RARsRbYm4cMe1Iyg JJycDAdwrCaIDe6SnxWIAYDuIwTI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67915.RARsRbYm4cMe1Iyg JJycDAdwrCaIDe6SnxWIAYDuIwTI130 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

NP67916.RAfghptP-hb1b24lN6P3RMDte1llVJC9y2s3IUGLzVNg4
has assertion: NP67916.RAfghptP-hb1b24lN6P3RMDte1llVJC9y2s3IUGLzVNg4130 assertion
has provenance: NP67916.RAfghptP-hb1b24lN6P3RMDte1llVJC9y2s3IUGLzVNg4130 provenance
has publication info: NP67916.RAfghptP-hb1b24lN6P3RMDte1llVJC9y2s3IUGLzVNg4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67916.RAfghptP-hb1b24lN6P3RMDte1llVJC9y2s3IUGLzVNg4130 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

NP67918.RAZkShhsOqbzDCjsp1-AOgjJaBHgVtop zafI39Uz3R5I
has assertion: NP67918.RAZkShhsOqbzDCjsp1-AOgjJaBHgVtop zafI39Uz3R5I130 assertion
has provenance: NP67918.RAZkShhsOqbzDCjsp1-AOgjJaBHgVtop zafI39Uz3R5I130 provenance
has publication info: NP67918.RAZkShhsOqbzDCjsp1-AOgjJaBHgVtop zafI39Uz3R5I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67918.RAZkShhsOqbzDCjsp1-AOgjJaBHgVtop zafI39Uz3R5I130 assertion
type: Assertion
description: [Common variants on chromosome 6p22.1 are associated 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/19571809
was generated by: ECO_0000203

NP67921.RAdNBFNI-1OBuNSoaDOmaNXfVoy-1DdoGlvzj1WuJ06wQ
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has publication info: NP67921.RAdNBFNI-1OBuNSoaDOmaNXfVoy-1DdoGlvzj1WuJ06wQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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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

NP67921.RAdNBFNI-1OBuNSoaDOmaNXfVoy-1DdoGlvzj1WuJ06wQ130 assertion
type: Assertion
description: [Association of SPINK1 gene mutation and CFTR gene polymorphisms in patients with pancreas divisum presenting with idiopathic 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/19593166
was generated by: ECO_0000203

NP67922.RAWpsYY2CnB59NevqSyLBgwocCnf1Mp6nBBFvEjMwXOSM
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has publication info: NP67922.RAWpsYY2CnB59NevqSyLBgwocCnf1Mp6nBBFvEjMwXOSM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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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

NP67922.RAWpsYY2CnB59NevqSyLBgwocCnf1Mp6nBBFvEjMwXOSM130 assertion
type: Assertion
description: [Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham 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/17903294
was generated by: ECO_0000203

NP67923.RAasv-66lnFk8ph3VT6LQ1tSOrt7dpFv 51LB3RH2WUzc
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP67923.RAasv-66lnFk8ph3VT6LQ1tSOrt7dpFv 51LB3RH2WUzc130 assertion
type: Assertion
description: [Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19578796
was generated by: ECO_0000203

NP67935.RAa3JpG1C7YYOLVGrj27X6o 2gPL9BS7ThoVdH61 UtUI
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67935.RAa3JpG1C7YYOLVGrj27X6o 2gPL9BS7ThoVdH61 UtUI130 assertion
type: Assertion
description: [Congenital thrombotic risk factors in beta-thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18480081
was generated by: ECO_0000203

NP67948.RAQ6UDBdccXSR5vpkJ1zJzeN2bY9dQ7-Ly5frCktSKOXY
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67948.RAQ6UDBdccXSR5vpkJ1zJzeN2bY9dQ7-Ly5frCktSKOXY130 assertion
type: Assertion
description: [Genetic variations in NR2A have the greatest relevance for human alcohol dependence among the glutamatergic genes selected for their known alteration of alcohol effects in animal models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18606955
was generated by: ECO_0000203

NP67951.RASDgMH47DCFZEBonWKfrEIVhYw6nVlABsP9zGsw4rbBw
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has publication info: NP67951.RASDgMH47DCFZEBonWKfrEIVhYw6nVlABsP9zGsw4rbBw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67951.RASDgMH47DCFZEBonWKfrEIVhYw6nVlABsP9zGsw4rbBw130 assertion
type: Assertion
description: [Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20379614
was generated by: ECO_0000203

NP67952.RAVlJEUN2cBxqpxyYkJr1sNFiMQEJk9Az2P8l8MLlRtdY
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67952.RAVlJEUN2cBxqpxyYkJr1sNFiMQEJk9Az2P8l8MLlRtdY130 assertion
type: Assertion
description: [Tagging single nucleotide polymorphisms in phosphoinositide-3-kinase-related protein kinase genes involved in DNA damage `checkpoints` and lung 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/18451257
was generated by: ECO_0000203

NP67954.RAXSgdtu65iaxJjw0lyk-F2dKUqpCs8RC5cIRbb3SXCDM
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67954.RAXSgdtu65iaxJjw0lyk-F2dKUqpCs8RC5cIRbb3SXCDM130 assertion
type: Assertion
description: [To investigate the association between the polymorphisms of the KU70 and X-ray repair cross complementing group 7 (XRCC7) genes and the 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/18422577
was generated by: ECO_0000203

NP67955.RAfZMv4wIvakhvqqH7ZndVjXKvHWVRhCj00iyCGQYQ5H8
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has publication info: NP67955.RAfZMv4wIvakhvqqH7ZndVjXKvHWVRhCj00iyCGQYQ5H8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67955.RAfZMv4wIvakhvqqH7ZndVjXKvHWVRhCj00iyCGQYQ5H8130 assertion
type: Assertion
description: [Genetic polymorphisms in 85 DNA repair genes and bladder 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/19237606
was generated by: ECO_0000203

NP67957.RAQSuxS45lyCxOgNXpPHnex5Lag7iBis-J5AS4F9m8hTo
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67957.RAQSuxS45lyCxOgNXpPHnex5Lag7iBis-J5AS4F9m8hTo130 assertion
type: Assertion
description: [Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic 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/19074885
was generated by: ECO_0000203

NP67958.RAQ82 0p-bC9qbUBPSIyM7vLv-MJbWTMX4Y7d3c4eXe0g
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has publication info: NP67958.RAQ82 0p-bC9qbUBPSIyM7vLv-MJbWTMX4Y7d3c4eXe0g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67958.RAQ82 0p-bC9qbUBPSIyM7vLv-MJbWTMX4Y7d3c4eXe0g130 assertion
type: Assertion
description: [Our results suggest that PRKCSH gene is not a major genetic cause of PCLD and there may be at least another locus responsible for the 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/19308730
was generated by: ECO_0000203

NP67960.RARbIGB1 64kPEElLIMzsqSBjvyvcyxtaig4P9C5kYY54
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has publication info: NP67960.RARbIGB1 64kPEElLIMzsqSBjvyvcyxtaig4P9C5kYY54130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67960.RARbIGB1 64kPEElLIMzsqSBjvyvcyxtaig4P9C5kYY54130 assertion
type: Assertion
description: [SNPs at T2DM susceptibility loci identified through GWAS in populations of European ancestry show similar effects in 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/19892838
was generated by: ECO_0000203

NP67962.RAQ51KR2fjkjLtYH25ctg7br-RZxKOQt4loVnL2wnrx5w
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP67962.RAQ51KR2fjkjLtYH25ctg7br-RZxKOQt4loVnL2wnrx5w130 assertion
type: Assertion
description: [Our study suggests that a small subset of GWAS-identified SNPs may increase T2D susceptibility by modulating expression of nearby transcripts in adipose or muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21084393
was generated by: ECO_0000203

NP67963.RASowv5jJwzyu2 9XPrVvCQokR1mEr3xPQurapr3vnCbQ
has assertion: NP67963.RASowv5jJwzyu2 9XPrVvCQokR1mEr3xPQurapr3vnCbQ130 assertion
has provenance: NP67963.RASowv5jJwzyu2 9XPrVvCQokR1mEr3xPQurapr3vnCbQ130 provenance
has publication info: NP67963.RASowv5jJwzyu2 9XPrVvCQokR1mEr3xPQurapr3vnCbQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67963.RASowv5jJwzyu2 9XPrVvCQokR1mEr3xPQurapr3vnCbQ130 assertion
type: Assertion
description: [We performed a genome-wide case-control study and found that a nonsynonymous SNP in PRKCH encoding a member of protein kinase C (PKCC eta) was significantly associated with brain 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/19198108
was generated by: ECO_0000203

NP67967.RASZ1RFW1C9xRVtkirPHhdJsaWUoJ6lhK1LOFSoqeO6NQ
has assertion: NP67967.RASZ1RFW1C9xRVtkirPHhdJsaWUoJ6lhK1LOFSoqeO6NQ130 assertion
has provenance: NP67967.RASZ1RFW1C9xRVtkirPHhdJsaWUoJ6lhK1LOFSoqeO6NQ130 provenance
has publication info: NP67967.RASZ1RFW1C9xRVtkirPHhdJsaWUoJ6lhK1LOFSoqeO6NQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67967.RASZ1RFW1C9xRVtkirPHhdJsaWUoJ6lhK1LOFSoqeO6NQ130 assertion
type: Assertion
description: [Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern 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/19367581
was generated by: ECO_0000203

NP67982.RAU9bWoSJaXVyN8elRWb0U HopoP0dGCGGfLEG2Am0368
has assertion: NP67982.RAU9bWoSJaXVyN8elRWb0U HopoP0dGCGGfLEG2Am0368130 assertion
has provenance: NP67982.RAU9bWoSJaXVyN8elRWb0U HopoP0dGCGGfLEG2Am0368130 provenance
has publication info: NP67982.RAU9bWoSJaXVyN8elRWb0U HopoP0dGCGGfLEG2Am0368130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67982.RAU9bWoSJaXVyN8elRWb0U HopoP0dGCGGfLEG2Am0368130 assertion
type: Assertion
description: [Mutations in the perforin gene can be linked to macrophage activation syndrome in patients with systemic onset 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/20019066
was generated by: ECO_0000203

NP67983.RAUjCzZAc2c9T6aEaORerqOxB QGK8Hj2MdxGoxDX5k4M
has assertion: NP67983.RAUjCzZAc2c9T6aEaORerqOxB QGK8Hj2MdxGoxDX5k4M130 assertion
has provenance: NP67983.RAUjCzZAc2c9T6aEaORerqOxB QGK8Hj2MdxGoxDX5k4M130 provenance
has publication info: NP67983.RAUjCzZAc2c9T6aEaORerqOxB QGK8Hj2MdxGoxDX5k4M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67983.RAUjCzZAc2c9T6aEaORerqOxB QGK8Hj2MdxGoxDX5k4M130 assertion
type: Assertion
description: [The results from this study provide evidence for the presence of genes affecting T2DM on chromosomes 4q, 12q, and 22q in AA; 6p in EA; 2p in AI; and 13q in MA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19795399
was generated by: ECO_0000203

NP67985.RAXzYa9V7ZZwCOyv01yO47UeUWOO-jDdGID Pxb4YL39M
has assertion: NP67985.RAXzYa9V7ZZwCOyv01yO47UeUWOO-jDdGID Pxb4YL39M130 assertion
has provenance: NP67985.RAXzYa9V7ZZwCOyv01yO47UeUWOO-jDdGID Pxb4YL39M130 provenance
has publication info: NP67985.RAXzYa9V7ZZwCOyv01yO47UeUWOO-jDdGID Pxb4YL39M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67985.RAXzYa9V7ZZwCOyv01yO47UeUWOO-jDdGID Pxb4YL39M130 assertion
type: Assertion
description: [Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet 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/19536175
was generated by: ECO_0000203

NP67988.RAei6fohj-U38jSMp q-Te0RaBnYcpG6HaDJyQWxf RBo
has assertion: NP67988.RAei6fohj-U38jSMp q-Te0RaBnYcpG6HaDJyQWxf RBo130 assertion
has provenance: NP67988.RAei6fohj-U38jSMp q-Te0RaBnYcpG6HaDJyQWxf RBo130 provenance
has publication info: NP67988.RAei6fohj-U38jSMp q-Te0RaBnYcpG6HaDJyQWxf RBo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67988.RAei6fohj-U38jSMp q-Te0RaBnYcpG6HaDJyQWxf RBo130 assertion
type: Assertion
description: [Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white 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/19064572
was generated by: ECO_0000203

NP67990.RAVOc7seXO6n27LsZBk6uQOfuThHp zMox52d0VSbDvfQ
has assertion: NP67990.RAVOc7seXO6n27LsZBk6uQOfuThHp zMox52d0VSbDvfQ130 assertion
has provenance: NP67990.RAVOc7seXO6n27LsZBk6uQOfuThHp zMox52d0VSbDvfQ130 provenance
has publication info: NP67990.RAVOc7seXO6n27LsZBk6uQOfuThHp zMox52d0VSbDvfQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67990.RAVOc7seXO6n27LsZBk6uQOfuThHp zMox52d0VSbDvfQ130 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

NP67992.RAQOtDxWRGaeeOQBBliUEkqzCeplMRVfwT31 0Z9OrzG0
has assertion: NP67992.RAQOtDxWRGaeeOQBBliUEkqzCeplMRVfwT31 0Z9OrzG0130 assertion
has provenance: NP67992.RAQOtDxWRGaeeOQBBliUEkqzCeplMRVfwT31 0Z9OrzG0130 provenance
has publication info: NP67992.RAQOtDxWRGaeeOQBBliUEkqzCeplMRVfwT31 0Z9OrzG0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP67992.RAQOtDxWRGaeeOQBBliUEkqzCeplMRVfwT31 0Z9OrzG0130 assertion
type: Assertion
description: [A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for 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/19838195
was generated by: ECO_0000203

NP68001.RAcIOebd3FjgmFgrDFyuA3aC9e MffBQhwfQV2MKe0goM
has assertion: NP68001.RAcIOebd3FjgmFgrDFyuA3aC9e MffBQhwfQV2MKe0goM130 assertion
has provenance: NP68001.RAcIOebd3FjgmFgrDFyuA3aC9e MffBQhwfQV2MKe0goM130 provenance
has publication info: NP68001.RAcIOebd3FjgmFgrDFyuA3aC9e MffBQhwfQV2MKe0goM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68001.RAcIOebd3FjgmFgrDFyuA3aC9e MffBQhwfQV2MKe0goM130 assertion
type: Assertion
description: [Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19734900
was generated by: ECO_0000203

NP68002.RAQH2kuy13sRiArG8IhJbOYUmOg1yWZvV xYMyLmDv4xU
has assertion: NP68002.RAQH2kuy13sRiArG8IhJbOYUmOg1yWZvV xYMyLmDv4xU130 assertion
has provenance: NP68002.RAQH2kuy13sRiArG8IhJbOYUmOg1yWZvV xYMyLmDv4xU130 provenance
has publication info: NP68002.RAQH2kuy13sRiArG8IhJbOYUmOg1yWZvV xYMyLmDv4xU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68002.RAQH2kuy13sRiArG8IhJbOYUmOg1yWZvV xYMyLmDv4xU130 assertion
type: Assertion
description: [Protein phosphatase 2A subunit gene haplotypes and proliferative breast disease modify 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/19890961
was generated by: ECO_0000203

NP68012.RAeGrlsafsOX1eGcMumHwcXeBSmhWmT1O9wuhU8n4JbXY
has assertion: NP68012.RAeGrlsafsOX1eGcMumHwcXeBSmhWmT1O9wuhU8n4JbXY130 assertion
has provenance: NP68012.RAeGrlsafsOX1eGcMumHwcXeBSmhWmT1O9wuhU8n4JbXY130 provenance
has publication info: NP68012.RAeGrlsafsOX1eGcMumHwcXeBSmhWmT1O9wuhU8n4JbXY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68012.RAeGrlsafsOX1eGcMumHwcXeBSmhWmT1O9wuhU8n4JbXY130 assertion
type: Assertion
description: [Clinical information of 963 heart failure patients was analyzed according to race, inhibitor-1 genotype, treatment with beta-blockers and mortality patterns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18698139
was generated by: ECO_0000203

NP68022.RAcG 2107lWo0E1M-ENsznI5hfF9JzkLLcIDY4jAvZUPc
has assertion: NP68022.RAcG 2107lWo0E1M-ENsznI5hfF9JzkLLcIDY4jAvZUPc130 assertion
has provenance: NP68022.RAcG 2107lWo0E1M-ENsznI5hfF9JzkLLcIDY4jAvZUPc130 provenance
has publication info: NP68022.RAcG 2107lWo0E1M-ENsznI5hfF9JzkLLcIDY4jAvZUPc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68022.RAcG 2107lWo0E1M-ENsznI5hfF9JzkLLcIDY4jAvZUPc130 assertion
type: Assertion
description: [The PPARGC1A Gly482Ser polymorphism is associated with left ventricular diastolic dysfunction in 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/19077249
was generated by: ECO_0000203

NP68029.RAbjteFPWCCTgNk6HfD qUXCmeC 5rPTnmxj66uP8w6bU
has assertion: NP68029.RAbjteFPWCCTgNk6HfD qUXCmeC 5rPTnmxj66uP8w6bU130 assertion
has provenance: NP68029.RAbjteFPWCCTgNk6HfD qUXCmeC 5rPTnmxj66uP8w6bU130 provenance
has publication info: NP68029.RAbjteFPWCCTgNk6HfD qUXCmeC 5rPTnmxj66uP8w6bU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68029.RAbjteFPWCCTgNk6HfD qUXCmeC 5rPTnmxj66uP8w6bU130 assertion
type: Assertion
description: [Twenty-three polymorphisms in 22 potential PAD candidate genes (F2, FGB, MTHFR, ITGB3, ACE, AGT, IL6, CCL2, ICAM1, SELE, MMP9, PPARG, MMP1, ADD1, P2RY12, LIPC, PLA2G7, SCARB1, MMP3, MTTP, LPA, CHRNA3) showed a significant association in individual 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/19435865
was generated by: ECO_0000203

NP68032.RAWjtEgT-XmWYcMJbQVEcVYK7o5Ld3vfyFd1abHjggsiA
has assertion: NP68032.RAWjtEgT-XmWYcMJbQVEcVYK7o5Ld3vfyFd1abHjggsiA130 assertion
has provenance: NP68032.RAWjtEgT-XmWYcMJbQVEcVYK7o5Ld3vfyFd1abHjggsiA130 provenance
has publication info: NP68032.RAWjtEgT-XmWYcMJbQVEcVYK7o5Ld3vfyFd1abHjggsiA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68032.RAWjtEgT-XmWYcMJbQVEcVYK7o5Ld3vfyFd1abHjggsiA130 assertion
type: Assertion
description: [The polymorphism IL-1beta T-31C is associated with a longer overall survival in patients with multiple myeloma undergoing auto-SCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18997828
was generated by: ECO_0000203

NP68039.RAZP2IzkmW6qrUv4ryZXRp9OgQVFvfyqCL7DzpPR7EAZw
has assertion: NP68039.RAZP2IzkmW6qrUv4ryZXRp9OgQVFvfyqCL7DzpPR7EAZw130 assertion
has provenance: NP68039.RAZP2IzkmW6qrUv4ryZXRp9OgQVFvfyqCL7DzpPR7EAZw130 provenance
has publication info: NP68039.RAZP2IzkmW6qrUv4ryZXRp9OgQVFvfyqCL7DzpPR7EAZw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68039.RAZP2IzkmW6qrUv4ryZXRp9OgQVFvfyqCL7DzpPR7EAZw130 assertion
type: Assertion
description: [The association of olanzapine-induced weight gain with peroxisome proliferator-activated receptor-gamma2 Pro12Ala polymorphism in patients 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/19622037
was generated by: ECO_0000203

NP68043.RAdi67dJI6GA3nDhduKIW 8ZPBX-3gaNzOh4EVKK9uFkE
has assertion: NP68043.RAdi67dJI6GA3nDhduKIW 8ZPBX-3gaNzOh4EVKK9uFkE130 assertion
has provenance: NP68043.RAdi67dJI6GA3nDhduKIW 8ZPBX-3gaNzOh4EVKK9uFkE130 provenance
has publication info: NP68043.RAdi67dJI6GA3nDhduKIW 8ZPBX-3gaNzOh4EVKK9uFkE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68043.RAdi67dJI6GA3nDhduKIW 8ZPBX-3gaNzOh4EVKK9uFkE130 assertion
type: Assertion
description: [To test the occurrence of the Pro12Ala mutation of the peroxisome proliferator-activated receptor- (PPAR)2-gene in patients with non-alcoholic fatty liver disease (NAFLD) or alcoholic fatty liver disease (AFLD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21155004
was generated by: ECO_0000203

NP68044.RAe7i9ARRjn8q6uQlRgV3DPF2ds7adLH8wwq6ouQ W9jM
has assertion: NP68044.RAe7i9ARRjn8q6uQlRgV3DPF2ds7adLH8wwq6ouQ W9jM130 assertion
has provenance: NP68044.RAe7i9ARRjn8q6uQlRgV3DPF2ds7adLH8wwq6ouQ W9jM130 provenance
has publication info: NP68044.RAe7i9ARRjn8q6uQlRgV3DPF2ds7adLH8wwq6ouQ W9jM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68044.RAe7i9ARRjn8q6uQlRgV3DPF2ds7adLH8wwq6ouQ W9jM130 assertion
type: Assertion
description: [Effect of peroxisome proliferator-activated receptors-gamma and co-activator-1alpha genetic polymorphisms on plasma adiponectin levels and susceptibility of non-alcoholic fatty liver disease in Chinese 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/17999673
was generated by: ECO_0000203

NP68047.RATd i Ji gSJYtlFHe7s7-wvNx4prA7S22ysZzOyEqPs
has assertion: NP68047.RATd i Ji gSJYtlFHe7s7-wvNx4prA7S22ysZzOyEqPs130 assertion
has provenance: NP68047.RATd i Ji gSJYtlFHe7s7-wvNx4prA7S22ysZzOyEqPs130 provenance
has publication info: NP68047.RATd i Ji gSJYtlFHe7s7-wvNx4prA7S22ysZzOyEqPs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68047.RATd i Ji gSJYtlFHe7s7-wvNx4prA7S22ysZzOyEqPs130 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

NP68054.RAWmoll2fIskPDnp9NZJGe7FagyZRLDSQnQbnY6Ym4aOs
has assertion: NP68054.RAWmoll2fIskPDnp9NZJGe7FagyZRLDSQnQbnY6Ym4aOs130 assertion
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has publication info: NP68054.RAWmoll2fIskPDnp9NZJGe7FagyZRLDSQnQbnY6Ym4aOs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68054.RAWmoll2fIskPDnp9NZJGe7FagyZRLDSQnQbnY6Ym4aOs130 assertion
type: Assertion
description: [Our data suggest that variants in FLNB and CRTAP at 3p are involved in BMD regulation in southern 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/19727905
was generated by: ECO_0000203

NP68056.RAaZomg2 uD2rvefG3LfEn5NkeCLa5xK8C3NFW-4zRAxA
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has provenance: NP68056.RAaZomg2 uD2rvefG3LfEn5NkeCLa5xK8C3NFW-4zRAxA130 provenance
has publication info: NP68056.RAaZomg2 uD2rvefG3LfEn5NkeCLa5xK8C3NFW-4zRAxA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68056.RAaZomg2 uD2rvefG3LfEn5NkeCLa5xK8C3NFW-4zRAxA130 assertion
type: Assertion
description: [Individual single tube genotyping and DNA pooling by allele-specific PCR to uncover associations of polymorphisms with complex 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/16999948
was generated by: ECO_0000203

NP68058.RAVvvclUmU4-rWVhkTjrPTIILjHWroTACIuXA8OZUT OQ
has assertion: NP68058.RAVvvclUmU4-rWVhkTjrPTIILjHWroTACIuXA8OZUT OQ130 assertion
has provenance: NP68058.RAVvvclUmU4-rWVhkTjrPTIILjHWroTACIuXA8OZUT OQ130 provenance
has publication info: NP68058.RAVvvclUmU4-rWVhkTjrPTIILjHWroTACIuXA8OZUT OQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68058.RAVvvclUmU4-rWVhkTjrPTIILjHWroTACIuXA8OZUT OQ130 assertion
type: Assertion
description: [Peroxisome proliferator-activated receptor gamma polymorphisms and coronary heart 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/20016803
was generated by: ECO_0000203

NP68059.RAd8OwCjeHfBW5D03gZj1GyVpPuBe5jNLtc9C8Dph-Jg0
has assertion: NP68059.RAd8OwCjeHfBW5D03gZj1GyVpPuBe5jNLtc9C8Dph-Jg0130 assertion
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has publication info: NP68059.RAd8OwCjeHfBW5D03gZj1GyVpPuBe5jNLtc9C8Dph-Jg0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68059.RAd8OwCjeHfBW5D03gZj1GyVpPuBe5jNLtc9C8Dph-Jg0130 assertion
type: Assertion
description: [Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19898482
was generated by: ECO_0000203

NP68065.RATRgkzgHNvcfi6KlUc5FK2ZAjMObfbRo8LIrHVGCDslc
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has publication info: NP68065.RATRgkzgHNvcfi6KlUc5FK2ZAjMObfbRo8LIrHVGCDslc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68065.RATRgkzgHNvcfi6KlUc5FK2ZAjMObfbRo8LIrHVGCDslc130 assertion
type: Assertion
description: [PPARD variation is clearly associated with a phenotype of reduced stature in both adults and 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/19383774
was generated by: ECO_0000203

NP68074.RAfJDFH5bUJGhzqPXbbAr-zEL3zyhRxxfOt Oz3XyWHDk
has assertion: NP68074.RAfJDFH5bUJGhzqPXbbAr-zEL3zyhRxxfOt Oz3XyWHDk130 assertion
has provenance: NP68074.RAfJDFH5bUJGhzqPXbbAr-zEL3zyhRxxfOt Oz3XyWHDk130 provenance
has publication info: NP68074.RAfJDFH5bUJGhzqPXbbAr-zEL3zyhRxxfOt Oz3XyWHDk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68074.RAfJDFH5bUJGhzqPXbbAr-zEL3zyhRxxfOt Oz3XyWHDk130 assertion
type: Assertion
description: [Interaction between PPARA genotype and beta-blocker treatment influences clinical outcomes following acute coronary 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/18855529
was generated by: ECO_0000203

NP68080.RAT9FV9nPL0zhryDNXGkR4TDVbsvvrKqT1fOe81oyCowA
has assertion: NP68080.RAT9FV9nPL0zhryDNXGkR4TDVbsvvrKqT1fOe81oyCowA130 assertion
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has publication info: NP68080.RAT9FV9nPL0zhryDNXGkR4TDVbsvvrKqT1fOe81oyCowA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68080.RAT9FV9nPL0zhryDNXGkR4TDVbsvvrKqT1fOe81oyCowA130 assertion
type: Assertion
description: [Contribution of organic cation transporter 2 (OCT2) to cisplatin-induced nephrotoxicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19625999
was generated by: ECO_0000203

NP68086.RAc2Bic7lEVcgkfZYLrcmX2UlLlwQjZKUT0wTl8LOdnFo
has assertion: NP68086.RAc2Bic7lEVcgkfZYLrcmX2UlLlwQjZKUT0wTl8LOdnFo130 assertion
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has publication info: NP68086.RAc2Bic7lEVcgkfZYLrcmX2UlLlwQjZKUT0wTl8LOdnFo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68086.RAc2Bic7lEVcgkfZYLrcmX2UlLlwQjZKUT0wTl8LOdnFo130 assertion
type: Assertion
description: [There is genetic heterogeneity in CRC associations in Americans of African versus European descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20659471
was generated by: ECO_0000203

NP68090.RAY0yuu9MwDSCvI4XWe7JL46ADuSa6vR-bMEQuYmJxaNk
has assertion: NP68090.RAY0yuu9MwDSCvI4XWe7JL46ADuSa6vR-bMEQuYmJxaNk130 assertion
has provenance: NP68090.RAY0yuu9MwDSCvI4XWe7JL46ADuSa6vR-bMEQuYmJxaNk130 provenance
has publication info: NP68090.RAY0yuu9MwDSCvI4XWe7JL46ADuSa6vR-bMEQuYmJxaNk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68090.RAY0yuu9MwDSCvI4XWe7JL46ADuSa6vR-bMEQuYmJxaNk130 assertion
type: Assertion
description: [Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese 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/19258400
was generated by: ECO_0000203

NP68093.RAfS6SNGPx6wZEaYcTs oelW2KjlVW8eeCb bHCByiw04
has assertion: NP68093.RAfS6SNGPx6wZEaYcTs oelW2KjlVW8eeCb bHCByiw04130 assertion
has provenance: NP68093.RAfS6SNGPx6wZEaYcTs oelW2KjlVW8eeCb bHCByiw04130 provenance
has publication info: NP68093.RAfS6SNGPx6wZEaYcTs oelW2KjlVW8eeCb bHCByiw04130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68093.RAfS6SNGPx6wZEaYcTs oelW2KjlVW8eeCb bHCByiw04130 assertion
type: Assertion
description: [Paraoxonase gene mutations in amyotrophic lateral 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/20582942
was generated by: ECO_0000203

NP68097.RAYJnxvJxeHl--eLzf6CJdlZKB6Ct vdAU4Mg8UqWwIbs
has assertion: NP68097.RAYJnxvJxeHl--eLzf6CJdlZKB6Ct vdAU4Mg8UqWwIbs130 assertion
has provenance: NP68097.RAYJnxvJxeHl--eLzf6CJdlZKB6Ct vdAU4Mg8UqWwIbs130 provenance
has publication info: NP68097.RAYJnxvJxeHl--eLzf6CJdlZKB6Ct vdAU4Mg8UqWwIbs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68097.RAYJnxvJxeHl--eLzf6CJdlZKB6Ct vdAU4Mg8UqWwIbs130 assertion
type: Assertion
description: [These findings contribute to the increasing weight of evidence that genetic variants in the paraoxonase gene cluster are associated with amyotrophic lateral 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/18695162
was generated by: ECO_0000203

NP68100.RAWpkuFTAazTjSHr8VR8x8HYviAOrqEaJjz2 oI OG2xk
has assertion: NP68100.RAWpkuFTAazTjSHr8VR8x8HYviAOrqEaJjz2 oI OG2xk130 assertion
has provenance: NP68100.RAWpkuFTAazTjSHr8VR8x8HYviAOrqEaJjz2 oI OG2xk130 provenance
has publication info: NP68100.RAWpkuFTAazTjSHr8VR8x8HYviAOrqEaJjz2 oI OG2xk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68100.RAWpkuFTAazTjSHr8VR8x8HYviAOrqEaJjz2 oI OG2xk130 assertion
type: Assertion
description: [Association of genetic factors with clinical peculiarities of hypertensive disease in patients with burdened familial anamnesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19254215
was generated by: ECO_0000203

NP68104.RATKo3hiD5bR09DhPuQU5UYsjA7CkQcg T01JV9ks0IZc
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68104.RATKo3hiD5bR09DhPuQU5UYsjA7CkQcg T01JV9ks0IZc130 assertion
type: Assertion
description: [Evaluation of genetic damage in a Brazilian population occupationally exposed to pesticides and its correlation with polymorphisms in metabolizing 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/18550589
was generated by: ECO_0000203

NP68108.RAUHpBKhGOUyXEVHL-NzFuUX0nM-EeGuRDpIUT5OWBjuc
has assertion: NP68108.RAUHpBKhGOUyXEVHL-NzFuUX0nM-EeGuRDpIUT5OWBjuc130 assertion
has provenance: NP68108.RAUHpBKhGOUyXEVHL-NzFuUX0nM-EeGuRDpIUT5OWBjuc130 provenance
has publication info: NP68108.RAUHpBKhGOUyXEVHL-NzFuUX0nM-EeGuRDpIUT5OWBjuc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68108.RAUHpBKhGOUyXEVHL-NzFuUX0nM-EeGuRDpIUT5OWBjuc130 assertion
type: Assertion
description: [These findings contribute to the increasing weight of evidence that genetic variants in the paraoxonase gene cluster are associated with amyotrophic lateral 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/18695162
was generated by: ECO_0000203

NP68111.RASj9Q95A1MUCMXye55w7Er9 ZJYD0GVJ5OecJFVRvkWs
has assertion: NP68111.RASj9Q95A1MUCMXye55w7Er9 ZJYD0GVJ5OecJFVRvkWs130 assertion
has provenance: NP68111.RASj9Q95A1MUCMXye55w7Er9 ZJYD0GVJ5OecJFVRvkWs130 provenance
has publication info: NP68111.RASj9Q95A1MUCMXye55w7Er9 ZJYD0GVJ5OecJFVRvkWs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68111.RASj9Q95A1MUCMXye55w7Er9 ZJYD0GVJ5OecJFVRvkWs130 assertion
type: Assertion
description: [The aim of the present study was to identify an association between the -A162G polymorphism of the promoter region of the human PON1 gene and the risk of sALS in a Polish 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/20625960
was generated by: ECO_0000203

NP68112.RAdSIMOamSvH6nLJ1yWtVp7-dZ8IFa98rwmyllgls V1w
has assertion: NP68112.RAdSIMOamSvH6nLJ1yWtVp7-dZ8IFa98rwmyllgls V1w130 assertion
has provenance: NP68112.RAdSIMOamSvH6nLJ1yWtVp7-dZ8IFa98rwmyllgls V1w130 provenance
has publication info: NP68112.RAdSIMOamSvH6nLJ1yWtVp7-dZ8IFa98rwmyllgls V1w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68112.RAdSIMOamSvH6nLJ1yWtVp7-dZ8IFa98rwmyllgls V1w130 assertion
type: Assertion
description: [Recently, non-synonymous coding single nucleotide polymorphisms (SNPs), known to lower serum PON activity, have been associated with sporadic ALS (SALS) in a Polish 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/17702780
was generated by: ECO_0000203

NP68113.RAfwu8yfzCYZtSKloTGv97kjYK-104CildP6dTqML2hzU
has assertion: NP68113.RAfwu8yfzCYZtSKloTGv97kjYK-104CildP6dTqML2hzU130 assertion
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has publication info: NP68113.RAfwu8yfzCYZtSKloTGv97kjYK-104CildP6dTqML2hzU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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

NP68113.RAfwu8yfzCYZtSKloTGv97kjYK-104CildP6dTqML2hzU130 assertion
type: Assertion
description: [The measurement of the lactonase activity of paraoxonase-1 in the clinical evaluation of patients with chronic liver impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18977341
was generated by: ECO_0000203

NP68115.RAUGufwkjTNCIjvWoaOALGqe18nvJfhhNkDEnTjQnOAnw
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has publication info: NP68115.RAUGufwkjTNCIjvWoaOALGqe18nvJfhhNkDEnTjQnOAnw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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

NP68115.RAUGufwkjTNCIjvWoaOALGqe18nvJfhhNkDEnTjQnOAnw130 assertion
type: Assertion
description: [The PON1 192 AA genotype may play an important role as a risk factor for ovarian cancer in the Turkish population and the A and L alleles may be associated with early onset of 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/19454508
was generated by: ECO_0000203

NP68119.RAW8zXuvm2Cq9hb4xXubmdgTQeYZoAyvX2IRH NQgmkdQ
has assertion: NP68119.RAW8zXuvm2Cq9hb4xXubmdgTQeYZoAyvX2IRH NQgmkdQ130 assertion
has provenance: NP68119.RAW8zXuvm2Cq9hb4xXubmdgTQeYZoAyvX2IRH NQgmkdQ130 provenance
has publication info: NP68119.RAW8zXuvm2Cq9hb4xXubmdgTQeYZoAyvX2IRH NQgmkdQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68119.RAW8zXuvm2Cq9hb4xXubmdgTQeYZoAyvX2IRH NQgmkdQ130 assertion
type: Assertion
description: [No significant differences were found for PON1 activity between normal and obese 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/21078685
was generated by: ECO_0000203

NP68120.RAfbbnM4B3I1qPA6HlQv-vPkYZU2wormJwu67HPRv pqE
has assertion: NP68120.RAfbbnM4B3I1qPA6HlQv-vPkYZU2wormJwu67HPRv pqE130 assertion
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has publication info: NP68120.RAfbbnM4B3I1qPA6HlQv-vPkYZU2wormJwu67HPRv pqE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68120.RAfbbnM4B3I1qPA6HlQv-vPkYZU2wormJwu67HPRv pqE130 assertion
type: Assertion
description: [In patients, the QQ genotype was statistically less frequent, while the RR genotype frequency was somewhat less than in 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/19846948
was generated by: ECO_0000203

NP68124.RAasD7WUETelEv7FzA160qwK7Nmt q-wXNC705rmNBsrg
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has publication info: NP68124.RAasD7WUETelEv7FzA160qwK7Nmt q-wXNC705rmNBsrg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68124.RAasD7WUETelEv7FzA160qwK7Nmt q-wXNC705rmNBsrg130 assertion
type: Assertion
description: [MC1R variation and melanoma risk in the Swedish population in relation to clinical and pathological parameters.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19077144
was generated by: ECO_0000203

NP68127.RAW9DGc8vrW7XfnH0Ou1QpZIJUMyUInpVtq8jHGmnEr1U
has assertion: NP68127.RAW9DGc8vrW7XfnH0Ou1QpZIJUMyUInpVtq8jHGmnEr1U130 assertion
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has publication info: NP68127.RAW9DGc8vrW7XfnH0Ou1QpZIJUMyUInpVtq8jHGmnEr1U130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68127.RAW9DGc8vrW7XfnH0Ou1QpZIJUMyUInpVtq8jHGmnEr1U130 assertion
type: Assertion
description: [Severe obesity in Han Chinese was associated with 3 novel common SNPs for ESR1 and PPARgamma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19491387
was generated by: ECO_0000203

NP68132.RATmVg-2VXvmBtPhi31GcQmODlXyuITKpENUelxUltWg4
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68132.RATmVg-2VXvmBtPhi31GcQmODlXyuITKpENUelxUltWg4130 assertion
type: Assertion
description: [Genetic polymorphisms in 85 DNA repair genes and bladder 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/19237606
was generated by: ECO_0000203

NP68136.RAaOj2EcI46UCF5OijHTRcBnp4VPcJzEKJJ97x46fQpPY
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68136.RAaOj2EcI46UCF5OijHTRcBnp4VPcJzEKJJ97x46fQpPY130 assertion
type: Assertion
description: [Genetic polymorphisms in 85 DNA repair genes and bladder 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/19237606
was generated by: ECO_0000203

NP68137.RAYpfYLpw219UnqFVHR8t2P4JP7kW4o7BbHttJsqpcy1A
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has publication info: NP68137.RAYpfYLpw219UnqFVHR8t2P4JP7kW4o7BbHttJsqpcy1A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68137.RAYpfYLpw219UnqFVHR8t2P4JP7kW4o7BbHttJsqpcy1A130 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

NP68145.RAS-qSjsKKVBJMCq69onAawZVRBzusK4A94SmBA8mekvc
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has publication info: NP68145.RAS-qSjsKKVBJMCq69onAawZVRBzusK4A94SmBA8mekvc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68145.RAS-qSjsKKVBJMCq69onAawZVRBzusK4A94SmBA8mekvc130 assertion
type: Assertion
description: [Genetic polymorphisms in 85 DNA repair genes and bladder 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/19237606
was generated by: ECO_0000203

NP68153.RAcMrWAECdRU-bnR3XsrMcCHM9e5BQchGOgZ2wv3K4Ujw
has assertion: NP68153.RAcMrWAECdRU-bnR3XsrMcCHM9e5BQchGOgZ2wv3K4Ujw130 assertion
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has publication info: NP68153.RAcMrWAECdRU-bnR3XsrMcCHM9e5BQchGOgZ2wv3K4Ujw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68153.RAcMrWAECdRU-bnR3XsrMcCHM9e5BQchGOgZ2wv3K4Ujw130 assertion
type: Assertion
description: [Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18575922
was generated by: ECO_0000203

NP68156.RATcRIdN2k3ZiQWbSlm5JBF3KwUJmSxjVmf3PXd-Sq4tU
has assertion: NP68156.RATcRIdN2k3ZiQWbSlm5JBF3KwUJmSxjVmf3PXd-Sq4tU130 assertion
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68156.RATcRIdN2k3ZiQWbSlm5JBF3KwUJmSxjVmf3PXd-Sq4tU130 assertion
type: Assertion
description: [Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic 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/19074885
was generated by: ECO_0000203

NP68157.RAfYEm0fzSjoNfw1W7tnDBpK90s4DazY-zPEhCWucpijI
has assertion: NP68157.RAfYEm0fzSjoNfw1W7tnDBpK90s4DazY-zPEhCWucpijI130 assertion
has provenance: NP68157.RAfYEm0fzSjoNfw1W7tnDBpK90s4DazY-zPEhCWucpijI130 provenance
has publication info: NP68157.RAfYEm0fzSjoNfw1W7tnDBpK90s4DazY-zPEhCWucpijI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68157.RAfYEm0fzSjoNfw1W7tnDBpK90s4DazY-zPEhCWucpijI130 assertion
type: Assertion
description: [Genetic polymorphisms in 85 DNA repair genes and bladder 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/19237606
was generated by: ECO_0000203

NP68175.RAZNzvMThsYzfAlhOevqk3JUw2eA5y4J3SI4aDx0T01Ks
has assertion: NP68175.RAZNzvMThsYzfAlhOevqk3JUw2eA5y4J3SI4aDx0T01Ks130 assertion
has provenance: NP68175.RAZNzvMThsYzfAlhOevqk3JUw2eA5y4J3SI4aDx0T01Ks130 provenance
has publication info: NP68175.RAZNzvMThsYzfAlhOevqk3JUw2eA5y4J3SI4aDx0T01Ks130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68175.RAZNzvMThsYzfAlhOevqk3JUw2eA5y4J3SI4aDx0T01Ks130 assertion
type: Assertion
description: [Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19536092
was generated by: ECO_0000203

NP68178.RAam1MJBp8EDE2mw-80DffQ26KNHRAcyS6MG5jRK2D2Zo
has assertion: NP68178.RAam1MJBp8EDE2mw-80DffQ26KNHRAcyS6MG5jRK2D2Zo130 assertion
has provenance: NP68178.RAam1MJBp8EDE2mw-80DffQ26KNHRAcyS6MG5jRK2D2Zo130 provenance
has publication info: NP68178.RAam1MJBp8EDE2mw-80DffQ26KNHRAcyS6MG5jRK2D2Zo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68178.RAam1MJBp8EDE2mw-80DffQ26KNHRAcyS6MG5jRK2D2Zo130 assertion
type: Assertion
description: [we find some evidence that common variants in mismatch repair genes may contribute to survival 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/19115210
was generated by: ECO_0000203

NP68179.RAUCnxFUNUjOT9q TTjWwPkwTwUvYFmeqczJEp9 q3myU
has assertion: NP68179.RAUCnxFUNUjOT9q TTjWwPkwTwUvYFmeqczJEp9 q3myU130 assertion
has provenance: NP68179.RAUCnxFUNUjOT9q TTjWwPkwTwUvYFmeqczJEp9 q3myU130 provenance
has publication info: NP68179.RAUCnxFUNUjOT9q TTjWwPkwTwUvYFmeqczJEp9 q3myU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68179.RAUCnxFUNUjOT9q TTjWwPkwTwUvYFmeqczJEp9 q3myU130 assertion
type: Assertion
description: [Population-based study of the association of variants in mismatch repair genes with prostate cancer risk and outcomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20056646
was generated by: ECO_0000203

NP68193.RAborWr11kh gSvClYSSymN7Fp aBqt2HzhJeqScL602Q
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has publication info: NP68193.RAborWr11kh gSvClYSSymN7Fp aBqt2HzhJeqScL602Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68193.RAborWr11kh gSvClYSSymN7Fp aBqt2HzhJeqScL602Q130 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

NP68197.RAfWUtAQy4y5n jnn9PJF5T KHI6tDJD mulW9xR DrnU
has assertion: NP68197.RAfWUtAQy4y5n jnn9PJF5T KHI6tDJD mulW9xR DrnU130 assertion
has provenance: NP68197.RAfWUtAQy4y5n jnn9PJF5T KHI6tDJD mulW9xR DrnU130 provenance
has publication info: NP68197.RAfWUtAQy4y5n jnn9PJF5T KHI6tDJD mulW9xR DrnU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68197.RAfWUtAQy4y5n jnn9PJF5T KHI6tDJD mulW9xR DrnU130 assertion
type: Assertion
description: [Genetic variation in phospholipid transfer protein modulates lipoprotein profiles in hyperalphalipoproteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19013296
was generated by: ECO_0000203

NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp Ja0DTTDxNhtquPtAM
has assertion: NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp Ja0DTTDxNhtquPtAM130 assertion
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has publication info: NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp Ja0DTTDxNhtquPtAM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp Ja0DTTDxNhtquPtAM130 assertion
type: Assertion
description: [The minor A allele at PLIN4 was associated with higher risk of MS at baseline, whereas the PLIN6 SNP was associated with better weight loss, suggesting that these polymorphisms may predict outcome strategies based on multidisciplinary treatment for OCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18812483
was generated by: ECO_0000203

NP68210.RAZeWJYCOhKgD-ElE1QYD9FSdQnOiYUwby1776CRNShcw
has assertion: NP68210.RAZeWJYCOhKgD-ElE1QYD9FSdQnOiYUwby1776CRNShcw130 assertion
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has publication info: NP68210.RAZeWJYCOhKgD-ElE1QYD9FSdQnOiYUwby1776CRNShcw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68210.RAZeWJYCOhKgD-ElE1QYD9FSdQnOiYUwby1776CRNShcw130 assertion
type: Assertion
description: [Our findings support the view that relevant relationships between circadian clocks and the metabolic syndrome in humans exist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19470168
was generated by: ECO_0000203

NP68216.RAUNNThCj LLQ6w1eAlNhNJTw7mU8H1aAJOKRKqEvHkQY
has assertion: NP68216.RAUNNThCj LLQ6w1eAlNhNJTw7mU8H1aAJOKRKqEvHkQY130 assertion
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has publication info: NP68216.RAUNNThCj LLQ6w1eAlNhNJTw7mU8H1aAJOKRKqEvHkQY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68216.RAUNNThCj LLQ6w1eAlNhNJTw7mU8H1aAJOKRKqEvHkQY130 assertion
type: Assertion
description: [Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20628624
was generated by: ECO_0000203

NP68217.RATM 4jd4lUh8ZiEPurp NimKdQbErkAGAGgJiaDmbidc
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has publication info: NP68217.RATM 4jd4lUh8ZiEPurp NimKdQbErkAGAGgJiaDmbidc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68217.RATM 4jd4lUh8ZiEPurp NimKdQbErkAGAGgJiaDmbidc130 assertion
type: Assertion
description: [Genetic profiling of genes from the oxidative stress pathway among North and South 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/18720901
was generated by: ECO_0000203

NP68222.RAb1WMqR4a0uxI0H5TfjitZ5skkoRwEMYe9M1NTgUuUwY
has assertion: NP68222.RAb1WMqR4a0uxI0H5TfjitZ5skkoRwEMYe9M1NTgUuUwY130 assertion
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has publication info: NP68222.RAb1WMqR4a0uxI0H5TfjitZ5skkoRwEMYe9M1NTgUuUwY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68222.RAb1WMqR4a0uxI0H5TfjitZ5skkoRwEMYe9M1NTgUuUwY130 assertion
type: Assertion
description: [Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19578796
was generated by: ECO_0000203

NP68224.RAbT90L HXgmbHP0OvZRCgrzhb73n0o2KzFCfuMXEvBDo
has assertion: NP68224.RAbT90L HXgmbHP0OvZRCgrzhb73n0o2KzFCfuMXEvBDo130 assertion
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has publication info: NP68224.RAbT90L HXgmbHP0OvZRCgrzhb73n0o2KzFCfuMXEvBDo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68224.RAbT90L HXgmbHP0OvZRCgrzhb73n0o2KzFCfuMXEvBDo130 assertion
type: Assertion
description: [Genetic deficiency of plasma lipoprotein-associated phospholipase A2 (PLA2G7 V297F null mutation) and risk of Alzheimer's disease in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20634581
was generated by: ECO_0000203

NP68226.RAXqJaaQOxsoMShol6P3QqvTmXOegXs-2ZztKIovDa5 4
has assertion: NP68226.RAXqJaaQOxsoMShol6P3QqvTmXOegXs-2ZztKIovDa5 4130 assertion
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68226.RAXqJaaQOxsoMShol6P3QqvTmXOegXs-2ZztKIovDa5 4130 assertion
type: Assertion
description: [We sought to determine whether allelic variants in the human PAFAH gene (Arg92His, Ile198Thr, and Ala379Val) contribute to variability in PAF-AH activity in patient plasma obtained within 72 h of ARDS 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/19583678
was generated by: ECO_0000203

NP68233.RAfxkBFVefRDZfDgEtwzZOsvjYSoBiyIQwW6ee3OdhTMc
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68233.RAfxkBFVefRDZfDgEtwzZOsvjYSoBiyIQwW6ee3OdhTMc130 assertion
type: Assertion
description: [Centrosome-related genes, genetic variation, and 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/20508983
was generated by: ECO_0000203

NP68237.RASt3qg7OwXr1Ro9b7p0NQXdgpD6mb1d8OwWWHpFps1Us
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68237.RASt3qg7OwXr1Ro9b7p0NQXdgpD6mb1d8OwWWHpFps1Us130 assertion
type: Assertion
description: [Novel susceptibility loci for second primary tumors/recurrence in head and neck cancer patients: large-scale evaluation of 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/19584075
was generated by: ECO_0000203

NP68238.RAVbQGioJ5fwYXzHo3YuL7c5DNwxNnpuZCutcLzPU3HHg
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has publication info: NP68238.RAVbQGioJ5fwYXzHo3YuL7c5DNwxNnpuZCutcLzPU3HHg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68238.RAVbQGioJ5fwYXzHo3YuL7c5DNwxNnpuZCutcLzPU3HHg130 assertion
type: Assertion
description: [Neurodegeneration associated with genetic defects in phospholipase A(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/18799783
was generated by: ECO_0000203

NP68242.RAV6abXUnkFa-FojRT8NpMr U0YFeQlF3TIzVuZCgaQfQ
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has publication info: NP68242.RAV6abXUnkFa-FojRT8NpMr U0YFeQlF3TIzVuZCgaQfQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68242.RAV6abXUnkFa-FojRT8NpMr U0YFeQlF3TIzVuZCgaQfQ130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP68245.RAZmoPMn93f6kxTjx7SaxSbTje1MbkaOKUhKCzmdVkq2c
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has publication info: NP68245.RAZmoPMn93f6kxTjx7SaxSbTje1MbkaOKUhKCzmdVkq2c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP68245.RAZmoPMn93f6kxTjx7SaxSbTje1MbkaOKUhKCzmdVkq2c130 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

NP68249.RAcpbLQDy4jmEsR q20l0Im4pgsYp -axlI4h6epKD3I0
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68249.RAcpbLQDy4jmEsR q20l0Im4pgsYp -axlI4h6epKD3I0130 assertion
type: Assertion
description: [Phospholipase A2 and cyclooxygenase 2 genes influence the risk of interferon-alpha-induced depression by regulating polyunsaturated fatty acids 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/20034614
was generated by: ECO_0000203

NP68250.RAb8ePBoIoSOQo02370OCHldKBtRjeZDijMY9JkjkPEI4
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68250.RAb8ePBoIoSOQo02370OCHldKBtRjeZDijMY9JkjkPEI4130 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

NP68255.RAVWFBw0v42kqSjhEVvtJsABJ 4z7FiMrnq99TTRgWeSM
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68255.RAVWFBw0v42kqSjhEVvtJsABJ 4z7FiMrnq99TTRgWeSM130 assertion
type: Assertion
description: [In this first study applying new TFC to patients suspected of ARVD/C, 64% of probable ARVD/C patients and 11% of family members were additionally diagnosed. ECG criteria and pathogenic mutations especially contributed to new diagnosis. Newly proposed TFC have a major impact in increasing diagnostic yield of ARVD/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/20215590
was generated by: ECO_0000203

NP68258.RAS1ldhh3 f1DOT7Lt-h5cy1pIvqPhjZxVB0PhsEvUxwk
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68258.RAS1ldhh3 f1DOT7Lt-h5cy1pIvqPhjZxVB0PhsEvUxwk130 assertion
type: Assertion
description: [Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20379614
was generated by: ECO_0000203

NP68262.RAcDsuP1ahjd7fh0eflgoCEgdv2dkKAboHq8y6Pdys6aQ
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68262.RAcDsuP1ahjd7fh0eflgoCEgdv2dkKAboHq8y6Pdys6aQ130 assertion
type: Assertion
description: [To verify their findings and to determine the nature of the association in a subset of our PD patients we have analyzed two PITX3 SNPs (rs2281983 and rs4919621) in 265 PD patients and compared them with 210 age-matched 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/19394114
was generated by: ECO_0000203

NP68264.RASe6e0W6RbhUgWdARdR-6NNioC r5AeiUsSkeigMYDWU
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68264.RASe6e0W6RbhUgWdARdR-6NNioC r5AeiUsSkeigMYDWU130 assertion
type: Assertion
description: [, we report the variation in genes of a pathway that has been involved in dopaminergic neuron differentiation and 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/20468068
was generated by: ECO_0000203

NP68274.RAbAa4pjMkRifHLfkV-BXDY8eHv9 TRahzU2jwkAxZ-N0
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68274.RAbAa4pjMkRifHLfkV-BXDY8eHv9 TRahzU2jwkAxZ-N0130 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

NP68278.RAarTcSAHtTzIJQ3w17oNnfUHFQMtgi9ntL 8b5kCyRhA
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68278.RAarTcSAHtTzIJQ3w17oNnfUHFQMtgi9ntL 8b5kCyRhA130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP68289.RAeOgn8UxyvkZAzMK6bivpSz3rwG3spAeCK1UqFG9GwgU
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68289.RAeOgn8UxyvkZAzMK6bivpSz3rwG3spAeCK1UqFG9GwgU130 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

NP68291.RASoEDH6zuuYTOoLVXUZ-Y6981N 8-LUMP dqNXwgG34
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68291.RASoEDH6zuuYTOoLVXUZ-Y6981N 8-LUMP dqNXwgG34130 assertion
type: Assertion
description: [PIK3CA mutation is associated with poor prognosis among patients with curatively resected colon 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/19237633
was generated by: ECO_0000203

NP68293.RATG6GlZIja-gzyKnfDYIXTe-YDroDJI O75wpU rroyc
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68293.RATG6GlZIja-gzyKnfDYIXTe-YDroDJI O75wpU rroyc130 assertion
type: Assertion
description: [Rare mutations in the PIK3CA gene contribute to aggressive endometrial 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/19839777
was generated by: ECO_0000203

NP68297.RAch1M8YhVQjvMzXvD-GjleenVtW6eA8Wkb7vZtQNuh2s
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP68297.RAch1M8YhVQjvMzXvD-GjleenVtW6eA8Wkb7vZtQNuh2s130 assertion
type: Assertion
description: [Genetic mutations associated with cigarette smoking 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/19351817
was generated by: ECO_0000203

NP68299.RAbXe-ueqDx4UZwz9XEG7Tl0cD7Dh1IWewfk8N1NNXOGs
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68299.RAbXe-ueqDx4UZwz9XEG7Tl0cD7Dh1IWewfk8N1NNXOGs130 assertion
type: Assertion
description: [PIK3CA mutations mostly begin to develop in ductal carcinoma of the breast.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19818761
was generated by: ECO_0000203

NP68311.RAVv2LW4vmYWtpFvtNiDXrmSnav3gytqIIxNoBKaESF9s
has assertion: NP68311.RAVv2LW4vmYWtpFvtNiDXrmSnav3gytqIIxNoBKaESF9s130 assertion
has provenance: NP68311.RAVv2LW4vmYWtpFvtNiDXrmSnav3gytqIIxNoBKaESF9s130 provenance
has publication info: NP68311.RAVv2LW4vmYWtpFvtNiDXrmSnav3gytqIIxNoBKaESF9s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68311.RAVv2LW4vmYWtpFvtNiDXrmSnav3gytqIIxNoBKaESF9s130 assertion
type: Assertion
description: [Genetic polymorphisms of peptidase inhibitor 3 (elafin) are associated with acute respiratory distress 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/19251943
was generated by: ECO_0000203

NP68313.RARD51ayYkI21DY8LQMWMjjsqDCt0qYKSq6q1p7gh9deU
has assertion: NP68313.RARD51ayYkI21DY8LQMWMjjsqDCt0qYKSq6q1p7gh9deU130 assertion
has provenance: NP68313.RARD51ayYkI21DY8LQMWMjjsqDCt0qYKSq6q1p7gh9deU130 provenance
has publication info: NP68313.RARD51ayYkI21DY8LQMWMjjsqDCt0qYKSq6q1p7gh9deU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68313.RARD51ayYkI21DY8LQMWMjjsqDCt0qYKSq6q1p7gh9deU130 assertion
type: Assertion
description: [Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20379614
was generated by: ECO_0000203

NP68316.RAT19IwJ9Vdp9tNUa7304g-T8NVdx8nhTKX NTZRrCY-E
has assertion: NP68316.RAT19IwJ9Vdp9tNUa7304g-T8NVdx8nhTKX NTZRrCY-E130 assertion
has provenance: NP68316.RAT19IwJ9Vdp9tNUa7304g-T8NVdx8nhTKX NTZRrCY-E130 provenance
has publication info: NP68316.RAT19IwJ9Vdp9tNUa7304g-T8NVdx8nhTKX NTZRrCY-E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68316.RAT19IwJ9Vdp9tNUa7304g-T8NVdx8nhTKX NTZRrCY-E130 assertion
type: Assertion
description: [Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic 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/18384079
was generated by: ECO_0000203

NP68317.RAVskaw7vQ8lQEJep5zK0rRCEtkRUBg1THweRnJffgx0Y
has assertion: NP68317.RAVskaw7vQ8lQEJep5zK0rRCEtkRUBg1THweRnJffgx0Y130 assertion
has provenance: NP68317.RAVskaw7vQ8lQEJep5zK0rRCEtkRUBg1THweRnJffgx0Y130 provenance
has publication info: NP68317.RAVskaw7vQ8lQEJep5zK0rRCEtkRUBg1THweRnJffgx0Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68317.RAVskaw7vQ8lQEJep5zK0rRCEtkRUBg1THweRnJffgx0Y130 assertion
type: Assertion
description: [Association analysis of glycine- and serine-related genes in a Japanese population of patients 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/19223009
was generated by: ECO_0000203

NP68319.RAVTeGavsIM9wLYcYIbj9clvah2IfVqfGEZfGXW70oZls
has assertion: NP68319.RAVTeGavsIM9wLYcYIbj9clvah2IfVqfGEZfGXW70oZls130 assertion
has provenance: NP68319.RAVTeGavsIM9wLYcYIbj9clvah2IfVqfGEZfGXW70oZls130 provenance
has publication info: NP68319.RAVTeGavsIM9wLYcYIbj9clvah2IfVqfGEZfGXW70oZls130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68319.RAVTeGavsIM9wLYcYIbj9clvah2IfVqfGEZfGXW70oZls130 assertion
type: Assertion
description: [Ovarian cancer risk in Polish BRCA1 mutation carriers is not associated with the prohibitin 3' untranslated region 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/18397521
was generated by: ECO_0000203

NP68326.RAQTf-bmlIHh1kJ0ojq-2ER9GKjmD6xPL64J9zA2sFWm4
has assertion: NP68326.RAQTf-bmlIHh1kJ0ojq-2ER9GKjmD6xPL64J9zA2sFWm4130 assertion
has provenance: NP68326.RAQTf-bmlIHh1kJ0ojq-2ER9GKjmD6xPL64J9zA2sFWm4130 provenance
has publication info: NP68326.RAQTf-bmlIHh1kJ0ojq-2ER9GKjmD6xPL64J9zA2sFWm4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68326.RAQTf-bmlIHh1kJ0ojq-2ER9GKjmD6xPL64J9zA2sFWm4130 assertion
type: Assertion
description: [Progesterone receptor (PROGINS) polymorphism and the risk of 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/18384825
was generated by: ECO_0000203

NP68329.RAdLblTMH 7j-2RWnYAOWhi10ghqgndXnh2 6FI1aGGU
has assertion: NP68329.RAdLblTMH 7j-2RWnYAOWhi10ghqgndXnh2 6FI1aGGU130 assertion
has provenance: NP68329.RAdLblTMH 7j-2RWnYAOWhi10ghqgndXnh2 6FI1aGGU130 provenance
has publication info: NP68329.RAdLblTMH 7j-2RWnYAOWhi10ghqgndXnh2 6FI1aGGU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68329.RAdLblTMH 7j-2RWnYAOWhi10ghqgndXnh2 6FI1aGGU130 assertion
type: Assertion
description: [Androgen, progesterone, and FSH receptor polymorphisms in ovarian cancer risk and 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/19458022
was generated by: ECO_0000203

NP68330.RAXXSrujmcy4OlGsa0GcIzmWji8Pfr44lE3M-o1xjj6VQ
has assertion: NP68330.RAXXSrujmcy4OlGsa0GcIzmWji8Pfr44lE3M-o1xjj6VQ130 assertion
has provenance: NP68330.RAXXSrujmcy4OlGsa0GcIzmWji8Pfr44lE3M-o1xjj6VQ130 provenance
has publication info: NP68330.RAXXSrujmcy4OlGsa0GcIzmWji8Pfr44lE3M-o1xjj6VQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68330.RAXXSrujmcy4OlGsa0GcIzmWji8Pfr44lE3M-o1xjj6VQ130 assertion
type: Assertion
description: [Androgen receptor cytosine, adenine, guanine repeats, and haplotypes in relation to ovarian 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/15994977
was generated by: ECO_0000203

NP68334.RAUPC9dEWgYGZ3zjhHF5mT02GWVroSVvr6LgigVrOPjdU
has assertion: NP68334.RAUPC9dEWgYGZ3zjhHF5mT02GWVroSVvr6LgigVrOPjdU130 assertion
has provenance: NP68334.RAUPC9dEWgYGZ3zjhHF5mT02GWVroSVvr6LgigVrOPjdU130 provenance
has publication info: NP68334.RAUPC9dEWgYGZ3zjhHF5mT02GWVroSVvr6LgigVrOPjdU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68334.RAUPC9dEWgYGZ3zjhHF5mT02GWVroSVvr6LgigVrOPjdU130 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

NP68335.RAfcYutZN8KlndEBRIfBIHSvw-c2cDBAtPnTNSy2XI5DQ
has assertion: NP68335.RAfcYutZN8KlndEBRIfBIHSvw-c2cDBAtPnTNSy2XI5DQ130 assertion
has provenance: NP68335.RAfcYutZN8KlndEBRIfBIHSvw-c2cDBAtPnTNSy2XI5DQ130 provenance
has publication info: NP68335.RAfcYutZN8KlndEBRIfBIHSvw-c2cDBAtPnTNSy2XI5DQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68335.RAfcYutZN8KlndEBRIfBIHSvw-c2cDBAtPnTNSy2XI5DQ130 assertion
type: Assertion
description: [Screening of 214 single nucleotide polymorphisms in 44 candidate cancer susceptibility genes: a case-control study on gastric and colorectal cancers 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/18510611
was generated by: ECO_0000203

NP68338.RATdRaN96SM7fClJ1MlBo3bshfmPy7OIFa171tisfz0hk
has assertion: NP68338.RATdRaN96SM7fClJ1MlBo3bshfmPy7OIFa171tisfz0hk130 assertion
has provenance: NP68338.RATdRaN96SM7fClJ1MlBo3bshfmPy7OIFa171tisfz0hk130 provenance
has publication info: NP68338.RATdRaN96SM7fClJ1MlBo3bshfmPy7OIFa171tisfz0hk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68338.RATdRaN96SM7fClJ1MlBo3bshfmPy7OIFa171tisfz0hk130 assertion
type: Assertion
description: [Allele and haplotype frequencies in the hPR are significantly different among women with preterm birth and women with preterm birth plus a family history of preterm birth. This suggests the hPR gene may be a candidate for association with preterm birth or familial 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/20308837
was generated by: ECO_0000203

NP68347.RATJopK-cLe6tq0oPnPc6cdIyl0bcXXqR4zPMsyRth9lo
has assertion: NP68347.RATJopK-cLe6tq0oPnPc6cdIyl0bcXXqR4zPMsyRth9lo130 assertion
has provenance: NP68347.RATJopK-cLe6tq0oPnPc6cdIyl0bcXXqR4zPMsyRth9lo130 provenance
has publication info: NP68347.RATJopK-cLe6tq0oPnPc6cdIyl0bcXXqR4zPMsyRth9lo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68347.RATJopK-cLe6tq0oPnPc6cdIyl0bcXXqR4zPMsyRth9lo130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP68359.RAblipQG7H6gnxvw0KI-ZJD7by9-GWv YRv81dHdXAcn8
has assertion: NP68359.RAblipQG7H6gnxvw0KI-ZJD7by9-GWv YRv81dHdXAcn8130 assertion
has provenance: NP68359.RAblipQG7H6gnxvw0KI-ZJD7by9-GWv YRv81dHdXAcn8130 provenance
has publication info: NP68359.RAblipQG7H6gnxvw0KI-ZJD7by9-GWv YRv81dHdXAcn8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68359.RAblipQG7H6gnxvw0KI-ZJD7by9-GWv YRv81dHdXAcn8130 assertion
type: Assertion
description: [Variants in circadian genes and prostate cancer risk: a population-based study in 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/17984998
was generated by: ECO_0000203

NP68363.RAZOSTKs6gBaDcs5F5z87FVzEsnGwb10AymIf yTnRG0o
has assertion: NP68363.RAZOSTKs6gBaDcs5F5z87FVzEsnGwb10AymIf yTnRG0o130 assertion
has provenance: NP68363.RAZOSTKs6gBaDcs5F5z87FVzEsnGwb10AymIf yTnRG0o130 provenance
has publication info: NP68363.RAZOSTKs6gBaDcs5F5z87FVzEsnGwb10AymIf yTnRG0o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68363.RAZOSTKs6gBaDcs5F5z87FVzEsnGwb10AymIf yTnRG0o130 assertion
type: Assertion
description: [Variants in circadian genes and prostate cancer risk: a population-based study in 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/17984998
was generated by: ECO_0000203

NP68367.RAZAr H8IJO8Zm7f7rwFwwaYRi-5rhSPlGRLHhkL-3D30
has assertion: NP68367.RAZAr H8IJO8Zm7f7rwFwwaYRi-5rhSPlGRLHhkL-3D30130 assertion
has provenance: NP68367.RAZAr H8IJO8Zm7f7rwFwwaYRi-5rhSPlGRLHhkL-3D30130 provenance
has publication info: NP68367.RAZAr H8IJO8Zm7f7rwFwwaYRi-5rhSPlGRLHhkL-3D30130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68367.RAZAr H8IJO8Zm7f7rwFwwaYRi-5rhSPlGRLHhkL-3D30130 assertion
type: Assertion
description: [Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/22158537
was generated by: ECO_0000203

NP68369.RAffq9qdRF-buQAhUdUFojwUWiiMdPlN-JXyKTgBwF-mM
has assertion: NP68369.RAffq9qdRF-buQAhUdUFojwUWiiMdPlN-JXyKTgBwF-mM130 assertion
has provenance: NP68369.RAffq9qdRF-buQAhUdUFojwUWiiMdPlN-JXyKTgBwF-mM130 provenance
has publication info: NP68369.RAffq9qdRF-buQAhUdUFojwUWiiMdPlN-JXyKTgBwF-mM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68369.RAffq9qdRF-buQAhUdUFojwUWiiMdPlN-JXyKTgBwF-mM130 assertion
type: Assertion
description: [Our data suggest that none of the investigated PEDF polymorphisms is likely a major risk factor for exudative AMD in a white European 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/19223990
was generated by: ECO_0000203

NP68372.RAUL6uCRCJCech4az4Wa2Hv4Y974uCVDwj8QUPSC7J4K4
has assertion: NP68372.RAUL6uCRCJCech4az4Wa2Hv4Y974uCVDwj8QUPSC7J4K4130 assertion
has provenance: NP68372.RAUL6uCRCJCech4az4Wa2Hv4Y974uCVDwj8QUPSC7J4K4130 provenance
has publication info: NP68372.RAUL6uCRCJCech4az4Wa2Hv4Y974uCVDwj8QUPSC7J4K4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68372.RAUL6uCRCJCech4az4Wa2Hv4Y974uCVDwj8QUPSC7J4K4130 assertion
type: Assertion
description: [To determine whether there is an association between complement factor H (CFH), high-temperature requirement A-1 (HTRA1), vascular endothelial growth factor (VEGF), and pigment epithelium-derived factor (PEDF) genotypes and response to treatment with photodynamic therapy (PDT) for age-related macular degeneration (AMD) 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/20678803
was generated by: ECO_0000203

NP68375.RAaqE8fdJff1UZfv7pdBXzNX2ja9JwcxLTM6ChlNsiZGQ
has assertion: NP68375.RAaqE8fdJff1UZfv7pdBXzNX2ja9JwcxLTM6ChlNsiZGQ130 assertion
has provenance: NP68375.RAaqE8fdJff1UZfv7pdBXzNX2ja9JwcxLTM6ChlNsiZGQ130 provenance
has publication info: NP68375.RAaqE8fdJff1UZfv7pdBXzNX2ja9JwcxLTM6ChlNsiZGQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68375.RAaqE8fdJff1UZfv7pdBXzNX2ja9JwcxLTM6ChlNsiZGQ130 assertion
type: Assertion
description: [Platelet-endothelial cell adhesion molecule-1 gene polymorphism and its soluble level are associated with ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19183069
was generated by: ECO_0000203

NP68376.RAWnmfHttQZhZiDVx UkPok4f-3fBExV9AUzTDKooQZWk
has assertion: NP68376.RAWnmfHttQZhZiDVx UkPok4f-3fBExV9AUzTDKooQZWk130 assertion
has provenance: NP68376.RAWnmfHttQZhZiDVx UkPok4f-3fBExV9AUzTDKooQZWk130 provenance
has publication info: NP68376.RAWnmfHttQZhZiDVx UkPok4f-3fBExV9AUzTDKooQZWk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68376.RAWnmfHttQZhZiDVx UkPok4f-3fBExV9AUzTDKooQZWk130 assertion
type: Assertion
description: [Platelet-endothelial cell adhesion molecule-1 gene polymorphism and its soluble level are associated with ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19183069
was generated by: ECO_0000203

NP68380.RAQrrpQbcPafGvBh9NdvzrbBvoZBkArPHbfL4S02JlsyI
has assertion: NP68380.RAQrrpQbcPafGvBh9NdvzrbBvoZBkArPHbfL4S02JlsyI130 assertion
has provenance: NP68380.RAQrrpQbcPafGvBh9NdvzrbBvoZBkArPHbfL4S02JlsyI130 provenance
has publication info: NP68380.RAQrrpQbcPafGvBh9NdvzrbBvoZBkArPHbfL4S02JlsyI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68380.RAQrrpQbcPafGvBh9NdvzrbBvoZBkArPHbfL4S02JlsyI130 assertion
type: Assertion
description: [Single-nucleotide polymorphism in codon 469 of ICAM-1 and codon 125 of PECAM-1 were examined in 158 patients with astrocytomas and 162 controls using polymerase chain reaction and restriction enzyme 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/19306055
was generated by: ECO_0000203

NP68383.RATSRA5lP9x0W nLaD20FHlOdbb7WC5xj AdcaDff7ZR0
has assertion: NP68383.RATSRA5lP9x0W nLaD20FHlOdbb7WC5xj AdcaDff7ZR0130 assertion
has provenance: NP68383.RATSRA5lP9x0W nLaD20FHlOdbb7WC5xj AdcaDff7ZR0130 provenance
has publication info: NP68383.RATSRA5lP9x0W nLaD20FHlOdbb7WC5xj AdcaDff7ZR0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68383.RATSRA5lP9x0W nLaD20FHlOdbb7WC5xj AdcaDff7ZR0130 assertion
type: Assertion
description: [Transcriptionally less active prodynorphin promoter alleles are associated with temporal lobe epilepsy: a case-control study 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/18334734
was generated by: ECO_0000203

NP68391.RAd2oaK2Pw-906SMQe6wuK3sv2k4aGWAyffk4dxW5Rojg
has assertion: NP68391.RAd2oaK2Pw-906SMQe6wuK3sv2k4aGWAyffk4dxW5Rojg130 assertion
has provenance: NP68391.RAd2oaK2Pw-906SMQe6wuK3sv2k4aGWAyffk4dxW5Rojg130 provenance
has publication info: NP68391.RAd2oaK2Pw-906SMQe6wuK3sv2k4aGWAyffk4dxW5Rojg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68391.RAd2oaK2Pw-906SMQe6wuK3sv2k4aGWAyffk4dxW5Rojg130 assertion
type: Assertion
description: [Interaction between BRCA1/BRCA2 and ATM/ATR associate with breast cancer susceptibility in a 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/20513533
was generated by: ECO_0000203

NP68399.RAQqrgZPEqkqsnCs8b80lD bTImaCCfdPevaA2vjLIIMA
has assertion: NP68399.RAQqrgZPEqkqsnCs8b80lD bTImaCCfdPevaA2vjLIIMA130 assertion
has provenance: NP68399.RAQqrgZPEqkqsnCs8b80lD bTImaCCfdPevaA2vjLIIMA130 provenance
has publication info: NP68399.RAQqrgZPEqkqsnCs8b80lD bTImaCCfdPevaA2vjLIIMA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68399.RAQqrgZPEqkqsnCs8b80lD bTImaCCfdPevaA2vjLIIMA130 assertion
type: Assertion
description: [This genetic epidemiological study demonstrated that 26.65% of the prelingual deafness in Northern Chinese patients can be detected at younger ages by genetic testing of three common hearing loss genes (GJB2, SLC26A4 and mtDNA A1555G), and thus, early intervention measures could be undertaken to help them in language acquisition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18274916
was generated by: ECO_0000203

NP68407.RAY0f6JepyYP2d8 pqw2-YY-8R0UKbkK7U7B8-hxYoM6E
has assertion: NP68407.RAY0f6JepyYP2d8 pqw2-YY-8R0UKbkK7U7B8-hxYoM6E130 assertion
has provenance: NP68407.RAY0f6JepyYP2d8 pqw2-YY-8R0UKbkK7U7B8-hxYoM6E130 provenance
has publication info: NP68407.RAY0f6JepyYP2d8 pqw2-YY-8R0UKbkK7U7B8-hxYoM6E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68407.RAY0f6JepyYP2d8 pqw2-YY-8R0UKbkK7U7B8-hxYoM6E130 assertion
type: Assertion
description: [The number of mutant alleles of SLC26A4, but not the presence of cochlear anomalies, has a significant association with severity of hearing loss in ears with EVA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19998422
was generated by: ECO_0000203

NP68413.RAQeIZ3W1oOUqDQwF eb3Pj0QRn91RLagIneUZu1o5gNo
has assertion: NP68413.RAQeIZ3W1oOUqDQwF eb3Pj0QRn91RLagIneUZu1o5gNo130 assertion
has provenance: NP68413.RAQeIZ3W1oOUqDQwF eb3Pj0QRn91RLagIneUZu1o5gNo130 provenance
has publication info: NP68413.RAQeIZ3W1oOUqDQwF eb3Pj0QRn91RLagIneUZu1o5gNo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68413.RAQeIZ3W1oOUqDQwF eb3Pj0QRn91RLagIneUZu1o5gNo130 assertion
type: Assertion
description: [Screening of SLC26A4 (PDS) gene mutation in cochlear implant recipients with inner ear malformation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18167283
was generated by: ECO_0000203

NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8
has assertion: NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130 assertion
has provenance: NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130 provenance
has publication info: NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130 assertion
type: Assertion
description: [To investigate the hot spot mutation of SLC26A4 gene and its incidence among patients with moderate to profound sensorineural hearing loss (SNHL) and to analyze the epidemiology of enlarged vestibular aqueduct syndrome in 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/18067822
was generated by: ECO_0000203

NP68415.RAS0a98Sfc1rng gb2Ubiymothkf4ISd5xqqE 36OmXVI
has assertion: NP68415.RAS0a98Sfc1rng gb2Ubiymothkf4ISd5xqqE 36OmXVI130 assertion
has provenance: NP68415.RAS0a98Sfc1rng gb2Ubiymothkf4ISd5xqqE 36OmXVI130 provenance
has publication info: NP68415.RAS0a98Sfc1rng gb2Ubiymothkf4ISd5xqqE 36OmXVI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68415.RAS0a98Sfc1rng gb2Ubiymothkf4ISd5xqqE 36OmXVI130 assertion
type: Assertion
description: [Genetic diagnosis and imaging results are the 2 predominant factors determining the outcome in children with cochlear implants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18316665
was generated by: ECO_0000203

NP68422.RAdPApwW5Gr5l-dTkRO6yx2xmlXjqwEoNXCv88QvJmKQk
has assertion: NP68422.RAdPApwW5Gr5l-dTkRO6yx2xmlXjqwEoNXCv88QvJmKQk130 assertion
has provenance: NP68422.RAdPApwW5Gr5l-dTkRO6yx2xmlXjqwEoNXCv88QvJmKQk130 provenance
has publication info: NP68422.RAdPApwW5Gr5l-dTkRO6yx2xmlXjqwEoNXCv88QvJmKQk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68422.RAdPApwW5Gr5l-dTkRO6yx2xmlXjqwEoNXCv88QvJmKQk130 assertion
type: Assertion
description: [This study was unable to find an association between KIT mutational status and clinical outcome of imatinib in Korean patients with advanced GISTs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19411681
was generated by: ECO_0000203

NP68435.RAcjYPBKUeehnLfrIAt4nmCWaF6aTwMiW6PrmgsNHluis
has assertion: NP68435.RAcjYPBKUeehnLfrIAt4nmCWaF6aTwMiW6PrmgsNHluis130 assertion
has provenance: NP68435.RAcjYPBKUeehnLfrIAt4nmCWaF6aTwMiW6PrmgsNHluis130 provenance
has publication info: NP68435.RAcjYPBKUeehnLfrIAt4nmCWaF6aTwMiW6PrmgsNHluis130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68435.RAcjYPBKUeehnLfrIAt4nmCWaF6aTwMiW6PrmgsNHluis130 assertion
type: Assertion
description: [PDE11A, PDE9A, and PDE1A are unlikely to play an important role in antidepressant outcome in this 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/19214142
was generated by: ECO_0000203

NP68439.RAbu5yh 6kG80zxAuHrxutxAUg8hked-nnnKCluUsfb0I
has assertion: NP68439.RAbu5yh 6kG80zxAuHrxutxAUg8hked-nnnKCluUsfb0I130 assertion
has provenance: NP68439.RAbu5yh 6kG80zxAuHrxutxAUg8hked-nnnKCluUsfb0I130 provenance
has publication info: NP68439.RAbu5yh 6kG80zxAuHrxutxAUg8hked-nnnKCluUsfb0I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68439.RAbu5yh 6kG80zxAuHrxutxAUg8hked-nnnKCluUsfb0I130 assertion
type: Assertion
description: [the results suggest a primary effect of PDE8B variants on cAMP levels in the thyroid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18514160
was generated by: ECO_0000203

NP68440.RAR7etcnnzv4aXH-ggMHlqdFHp3THumzr65C T2HafJ c
has assertion: NP68440.RAR7etcnnzv4aXH-ggMHlqdFHp3THumzr65C T2HafJ c130 assertion
has provenance: NP68440.RAR7etcnnzv4aXH-ggMHlqdFHp3THumzr65C T2HafJ c130 provenance
has publication info: NP68440.RAR7etcnnzv4aXH-ggMHlqdFHp3THumzr65C T2HafJ c130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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

NP68440.RAR7etcnnzv4aXH-ggMHlqdFHp3THumzr65C T2HafJ c130 assertion
type: Assertion
description: [We identified novel candidate genes for treatment response to risperidone and provide evidence that one of these additionally may confer susceptibility to 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/19850283
was generated by: ECO_0000203

NP68447.RAQKg iucbSgT75VN8RyE4YpjNImEZz-aIq7A0C0StIQo
has assertion: NP68447.RAQKg iucbSgT75VN8RyE4YpjNImEZz-aIq7A0C0StIQo130 assertion
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has publication info: NP68447.RAQKg iucbSgT75VN8RyE4YpjNImEZz-aIq7A0C0StIQo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68447.RAQKg iucbSgT75VN8RyE4YpjNImEZz-aIq7A0C0StIQo130 assertion
type: Assertion
description: [Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19578796
was generated by: ECO_0000203

NP68450.RAewWsGJ7qgwUc5vpSHKVqSXcKdbjwDftzPrOL0c2-EIc
has assertion: NP68450.RAewWsGJ7qgwUc5vpSHKVqSXcKdbjwDftzPrOL0c2-EIc130 assertion
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has publication info: NP68450.RAewWsGJ7qgwUc5vpSHKVqSXcKdbjwDftzPrOL0c2-EIc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68450.RAewWsGJ7qgwUc5vpSHKVqSXcKdbjwDftzPrOL0c2-EIc130 assertion
type: Assertion
description: [Genetic association and post-mortem brain mRNA analysis of DISC1 and related genes 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/19632097
was generated by: ECO_0000203

NP68452.RAUOUTiTZBuqzH3uW8ioX2mf5nhyy4l TO2aXpqqgzt1E
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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version: v2.1.0.0

NP68452.RAUOUTiTZBuqzH3uW8ioX2mf5nhyy4l TO2aXpqqgzt1E130 assertion
type: Assertion
description: [the SNPs of the PDE4D (83T/C) and IL-1 (-889C/T) were associated with increased risk for the development of IS in Northern Han 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/19786079
was generated by: ECO_0000203

NP68456.RAYgdoLkPTR5e3ursh7NjN5CcLGjuugvDx-WsVkZA1tVA
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68456.RAYgdoLkPTR5e3ursh7NjN5CcLGjuugvDx-WsVkZA1tVA130 assertion
type: Assertion
description: [Association of PDE11A global haplotype with major depression and antidepressant drug response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19557111
was generated by: ECO_0000203

NP68458.RAes7Bj1UX5JuHRpuLMEn0Jm3mAv3utl-zIRcRqVCbWFA
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68458.RAes7Bj1UX5JuHRpuLMEn0Jm3mAv3utl-zIRcRqVCbWFA130 assertion
type: Assertion
description: [PDE11A, PDE9A, and PDE1A are unlikely to play an important role in antidepressant outcome in this 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/19214142
was generated by: ECO_0000203

NP68467.RAWU2XzhRQo4HeJR2kzcM1ygftBTP2YMlZ6hFkO3rYMug
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68467.RAWU2XzhRQo4HeJR2kzcM1ygftBTP2YMlZ6hFkO3rYMug130 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

NP68468.RAbDq6K-evBEL8msjCgkYNvQAg6wKoiXUNoTfzSK6KY8A
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68468.RAbDq6K-evBEL8msjCgkYNvQAg6wKoiXUNoTfzSK6KY8A130 assertion
type: Assertion
description: [Our results suggested that the PD1 gene contributed to a genetic susceptibility to SSPE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20066438
was generated by: ECO_0000203

NP68470.RATlDUlPN8PUY1fugBJbNHBHWSIoo92055USetCAthYow
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP68470.RATlDUlPN8PUY1fugBJbNHBHWSIoo92055USetCAthYow130 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

NP68473.RAYLUsBzG0-Lc45uW5X1H n7vuJDC89Zxg2d85NRZypY0
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68473.RAYLUsBzG0-Lc45uW5X1H n7vuJDC89Zxg2d85NRZypY0130 assertion
type: Assertion
description: [rs1130409/T1865G (APEX1), rs1799782/T22142C (XRCC1), rs25487/G23990A (XRCC1), rs4989588/T3337A (FEN1), rs4989586/ G3259A (FEN1), rs4989587/C3315T (FEN1), and rs1050525/G6941T (PCNA) with breast 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/18669164
was generated by: ECO_0000203

NP68476.RAUGFWca2GWS2Re1QqyMjcO59Ssm7np8yxd03HrhTaBp4
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68476.RAUGFWca2GWS2Re1QqyMjcO59Ssm7np8yxd03HrhTaBp4130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP68477.RAR5i4os4ZF9dkYGV84dlx VIYHHNzTRObP VBOJbPS7A
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68477.RAR5i4os4ZF9dkYGV84dlx VIYHHNzTRObP VBOJbPS7A130 assertion
type: Assertion
description: [Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19536092
was generated by: ECO_0000203

NP68480.RAVDk385RCqeDtamMNmJ0eviR6GBWD5XGDaJ-f-F9E9Fs
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68480.RAVDk385RCqeDtamMNmJ0eviR6GBWD5XGDaJ-f-F9E9Fs130 assertion
type: Assertion
description: [Several gene variants in the Glycolysis were associated with schizophrenia in three independent 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/18460190
was generated by: ECO_0000203

NP68482.RAbeATUgiphDrwg5 uvkNgQk44oFxUJxajbqPwFe7kRxM
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68482.RAbeATUgiphDrwg5 uvkNgQk44oFxUJxajbqPwFe7kRxM130 assertion
type: Assertion
description: [Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19578796
was generated by: ECO_0000203

NP68484.RAQInOm6LKdWY36GhNYRTbKon3NtCSwBssKbnzSsRzQFQ
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68484.RAQInOm6LKdWY36GhNYRTbKon3NtCSwBssKbnzSsRzQFQ130 assertion
type: Assertion
description: [Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: preliminary evidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19054571
was generated by: ECO_0000203

NP68485.RASRoTc3DmS4D8XCfsQZDzftRpWbp05MxV5ArVHUfEfLI
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP68485.RASRoTc3DmS4D8XCfsQZDzftRpWbp05MxV5ArVHUfEfLI130 assertion
type: Assertion
description: [Genome-wide analysis of survival in 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/19414679
was generated by: ECO_0000203

NP68496.RAQM 4ZlvcZoVRfProTchTYJuTwd68fJhDi52qSAwAr5M
has assertion: NP68496.RAQM 4ZlvcZoVRfProTchTYJuTwd68fJhDi52qSAwAr5M130 assertion
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has publication info: NP68496.RAQM 4ZlvcZoVRfProTchTYJuTwd68fJhDi52qSAwAr5M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68496.RAQM 4ZlvcZoVRfProTchTYJuTwd68fJhDi52qSAwAr5M130 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

NP68503.RASMWWCkYUosyfWx8BgF9F 5dGTSa96b5PjWhMoh6ZdGc
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68503.RASMWWCkYUosyfWx8BgF9F 5dGTSa96b5PjWhMoh6ZdGc130 assertion
type: Assertion
description: [Our results revealed an association between high myopia and AC and AG dinucleotide repeat lengths in the PAX6 P1 promoter, indicating the involvement of PAX6 in the pathogenesis of high myopia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19907666
was generated by: ECO_0000203

NP68508.RARwYZrTdN1AAXmDkfkVOQGTMfEAfunIhWrwdv8iLLnGw
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has publication info: NP68508.RARwYZrTdN1AAXmDkfkVOQGTMfEAfunIhWrwdv8iLLnGw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP68508.RARwYZrTdN1AAXmDkfkVOQGTMfEAfunIhWrwdv8iLLnGw130 assertion
type: Assertion
description: [PAX6 mutations cause panocular malformations that vary considerably in pattern and 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/19218613
was generated by: ECO_0000203

NP68512.RATzTKI8xQMt4i5vG1NV4-G2sN94ifFw8cc 9872SncjY
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has publication info: NP68512.RATzTKI8xQMt4i5vG1NV4-G2sN94ifFw8cc 9872SncjY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68512.RATzTKI8xQMt4i5vG1NV4-G2sN94ifFw8cc 9872SncjY130 assertion
type: Assertion
description: [Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19578796
was generated by: ECO_0000203

NP68515.RAZCV1BfOHf2CIpjSLVskhIgv8SSjCndu4p3KO8rtnRP4
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68515.RAZCV1BfOHf2CIpjSLVskhIgv8SSjCndu4p3KO8rtnRP4130 assertion
type: Assertion
description: [To investigate the association of polymorphisms of PAX1 gene with congenital scoliosis (CS) in Chinese Han population and the relationship between the PAX1 gene polymorphisms and the clinical phenotypes of CS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19080705
was generated by: ECO_0000203

NP68525.RATmOkdpMLNiO43vaK6KUKiywUCaF3ER576q2uClGYwGE
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68525.RATmOkdpMLNiO43vaK6KUKiywUCaF3ER576q2uClGYwGE130 assertion
type: Assertion
description: [We identified novel candidate genes for treatment response to risperidone and provide evidence that one of these additionally may confer susceptibility to 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/19850283
was generated by: ECO_0000203

NP68530.RASDtHZXpWfzuZ8do 7M1-xnOCtQp32GzBLbdIOh FJhY
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68530.RASDtHZXpWfzuZ8do 7M1-xnOCtQp32GzBLbdIOh FJhY130 assertion
type: Assertion
description: [Postoperative bleeding in cardiac surgery: the role of tranexamic acid in patients homozygous for the 5G polymorphism of the plasminogen activator inhibitor-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/18362590
was generated by: ECO_0000203

NP68539.RAS8xB6rg0ERAKpC22tIZ3JBr7PE MHpsl2XEZ6tFmC2w
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68539.RAS8xB6rg0ERAKpC22tIZ3JBr7PE MHpsl2XEZ6tFmC2w130 assertion
type: Assertion
description: [Thrombophilic gene polymorphisms are risk factors for unexplained infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18930220
was generated by: ECO_0000203

NP68548.RAeVOVHKflRUGcp9QvJkPuC5zD9cKu5-r-R9VaLjiAqnE
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68548.RAeVOVHKflRUGcp9QvJkPuC5zD9cKu5-r-R9VaLjiAqnE130 assertion
type: Assertion
description: [Hereditary thrombophilia promotes induction of nephrosclerosis leading to activation of intraglomerular blood clotting which contributes to CGN 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/19799197
was generated by: ECO_0000203

NP68553.RAY4uA5hN1k4nhvqa85xpor0aamYjztrKkANRjDfWABjg
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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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version: v2.1.0.0

NP68553.RAY4uA5hN1k4nhvqa85xpor0aamYjztrKkANRjDfWABjg130 assertion
type: Assertion
description: [We tested four genes phenylalanine hydroxylase (PAH), the serotonin transporter (SLC6A4), monoamine oxidase B (MAOB), and the gamma-aminobutyric acid A receptor beta-3 subunit (GABRB3) for their impact on five schizophrenia symptom factors: delusions, hallucinations, mania, depression, and negative 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/19268543
was generated by: ECO_0000203

NP68557.RAReOSkybLFP QPnDbyqwQAM71s4hzxonYGMdSdIlDtlQ
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68557.RAReOSkybLFP QPnDbyqwQAM71s4hzxonYGMdSdIlDtlQ130 assertion
type: Assertion
description: [Genetic association and post-mortem brain mRNA analysis of DISC1 and related genes 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/19632097
was generated by: ECO_0000203

NP68565.RAdJIBzyXDD67NyRm4khk1BGw-fORzLpjc-WkMcdEh1DU
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68565.RAdJIBzyXDD67NyRm4khk1BGw-fORzLpjc-WkMcdEh1DU130 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

NP68568.RAQTLzJ9xgTe7LhJ o02vLllaujliTHAt mCcfTB1Ky E
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68568.RAQTLzJ9xgTe7LhJ o02vLllaujliTHAt mCcfTB1Ky E130 assertion
type: Assertion
description: [P2RX7 Gln460Arg polymorphism is associated with depression among diabetic 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/18801407
was generated by: ECO_0000203

NP68569.RARDX rm2Tm-qYy2VI1fpohDy5J5t3t15Q6THzl6as0C0
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68569.RARDX rm2Tm-qYy2VI1fpohDy5J5t3t15Q6THzl6as0C0130 assertion
type: Assertion
description: [A population-based association study of candidate genes for depression and sleep disturbance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19548263
was generated by: ECO_0000203

NP68571.RAVBHUyqI9prdkfeYGkLOY9v64oeaO oqm3YSUl4YegOE
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68571.RAVBHUyqI9prdkfeYGkLOY9v64oeaO oqm3YSUl4YegOE130 assertion
type: Assertion
description: [Ambulatory blood pressure is associated with polymorphic variation in P2X receptor 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/18852390
was generated by: ECO_0000203

NP68598.RAaY03-vQr xO92iefni0Mh90OHqNHsz1I4zSiudMUuWw
has assertion: NP68598.RAaY03-vQr xO92iefni0Mh90OHqNHsz1I4zSiudMUuWw130 assertion
has provenance: NP68598.RAaY03-vQr xO92iefni0Mh90OHqNHsz1I4zSiudMUuWw130 provenance
has publication info: NP68598.RAaY03-vQr xO92iefni0Mh90OHqNHsz1I4zSiudMUuWw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68598.RAaY03-vQr xO92iefni0Mh90OHqNHsz1I4zSiudMUuWw130 assertion
type: Assertion
description: [Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic 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/19074885
was generated by: ECO_0000203

NP68609.RAfiDK0NFwZR9Z8YoMuC6SlaifWORU95KOTzi4iXbLwQA
has assertion: NP68609.RAfiDK0NFwZR9Z8YoMuC6SlaifWORU95KOTzi4iXbLwQA130 assertion
has provenance: NP68609.RAfiDK0NFwZR9Z8YoMuC6SlaifWORU95KOTzi4iXbLwQA130 provenance
has publication info: NP68609.RAfiDK0NFwZR9Z8YoMuC6SlaifWORU95KOTzi4iXbLwQA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68609.RAfiDK0NFwZR9Z8YoMuC6SlaifWORU95KOTzi4iXbLwQA130 assertion
type: Assertion
description: [Pharmacological effects of lipid-lowering drugs recapitulate with a larger amplitude the phenotypic effects of common variants within their target 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/18787507
was generated by: ECO_0000203

NP68614.RAQJJzyYjlDpMuVYwL8a eAdO51HsxkjbgimlpduqQxgE
has assertion: NP68614.RAQJJzyYjlDpMuVYwL8a eAdO51HsxkjbgimlpduqQxgE130 assertion
has provenance: NP68614.RAQJJzyYjlDpMuVYwL8a eAdO51HsxkjbgimlpduqQxgE130 provenance
has publication info: NP68614.RAQJJzyYjlDpMuVYwL8a eAdO51HsxkjbgimlpduqQxgE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68614.RAQJJzyYjlDpMuVYwL8a eAdO51HsxkjbgimlpduqQxgE130 assertion
type: Assertion
description: [Our results imply that OPTC and EPYC are unlikely to play a major role in high myopia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19844586
was generated by: ECO_0000203

NP68630.RAT7Edk02IirZRfknVeE8uP8ZynxoReSCDUdz jRlsFc4
has assertion: NP68630.RAT7Edk02IirZRfknVeE8uP8ZynxoReSCDUdz jRlsFc4130 assertion
has provenance: NP68630.RAT7Edk02IirZRfknVeE8uP8ZynxoReSCDUdz jRlsFc4130 provenance
has publication info: NP68630.RAT7Edk02IirZRfknVeE8uP8ZynxoReSCDUdz jRlsFc4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68630.RAT7Edk02IirZRfknVeE8uP8ZynxoReSCDUdz jRlsFc4130 assertion
type: Assertion
description: [Variation in the mu-opioid receptor gene (OPRM1) is associated with dispositional and neural sensitivity to social rejection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19706472
was generated by: ECO_0000203

NP68633.RAZ3skF0KWOiRoNlIQ9 r7wMweapDFjpPpwl2y CQ9uOM
has assertion: NP68633.RAZ3skF0KWOiRoNlIQ9 r7wMweapDFjpPpwl2y CQ9uOM130 assertion
has provenance: NP68633.RAZ3skF0KWOiRoNlIQ9 r7wMweapDFjpPpwl2y CQ9uOM130 provenance
has publication info: NP68633.RAZ3skF0KWOiRoNlIQ9 r7wMweapDFjpPpwl2y CQ9uOM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68633.RAZ3skF0KWOiRoNlIQ9 r7wMweapDFjpPpwl2y CQ9uOM130 assertion
type: Assertion
description: [Association of ABCB1/MDR1 and OPRM1 gene polymorphisms with morphine pain relief.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17898703
was generated by: ECO_0000203

NP68638.RAaCwPz4g8dsWQYTzKmmfquCG4YiY S-42k5rPu3RF6I8
has assertion: NP68638.RAaCwPz4g8dsWQYTzKmmfquCG4YiY S-42k5rPu3RF6I8130 assertion
has provenance: NP68638.RAaCwPz4g8dsWQYTzKmmfquCG4YiY S-42k5rPu3RF6I8130 provenance
has publication info: NP68638.RAaCwPz4g8dsWQYTzKmmfquCG4YiY S-42k5rPu3RF6I8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68638.RAaCwPz4g8dsWQYTzKmmfquCG4YiY S-42k5rPu3RF6I8130 assertion
type: Assertion
description: [Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger 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/19598235
was generated by: ECO_0000203

NP68645.RAfT69Ya5brEtSRheZtXIBoB6KOa0fxZVSPAXb4Sxow5E
has assertion: NP68645.RAfT69Ya5brEtSRheZtXIBoB6KOa0fxZVSPAXb4Sxow5E130 assertion
has provenance: NP68645.RAfT69Ya5brEtSRheZtXIBoB6KOa0fxZVSPAXb4Sxow5E130 provenance
has publication info: NP68645.RAfT69Ya5brEtSRheZtXIBoB6KOa0fxZVSPAXb4Sxow5E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68645.RAfT69Ya5brEtSRheZtXIBoB6KOa0fxZVSPAXb4Sxow5E130 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

NP68652.RAS5Tg4CgEN5gxP4NmGM7CNrf9Bu9hM56 yzgIj8a0ujw
has assertion: NP68652.RAS5Tg4CgEN5gxP4NmGM7CNrf9Bu9hM56 yzgIj8a0ujw130 assertion
has provenance: NP68652.RAS5Tg4CgEN5gxP4NmGM7CNrf9Bu9hM56 yzgIj8a0ujw130 provenance
has publication info: NP68652.RAS5Tg4CgEN5gxP4NmGM7CNrf9Bu9hM56 yzgIj8a0ujw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68652.RAS5Tg4CgEN5gxP4NmGM7CNrf9Bu9hM56 yzgIj8a0ujw130 assertion
type: Assertion
description: [137 patients with primary open angle glaucoma (67 patients with high-tension glaucoma (HTG), 70 patients with normal-tension glaucoma (NTG)) and 75 controls from the North East of England were 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/19581274
was generated by: ECO_0000203

NP68657.RAZY- 5QlkIWgvmFEDFGrw57nFh4yO2Wlvkto3xk28Cls
has assertion: NP68657.RAZY- 5QlkIWgvmFEDFGrw57nFh4yO2Wlvkto3xk28Cls130 assertion
has provenance: NP68657.RAZY- 5QlkIWgvmFEDFGrw57nFh4yO2Wlvkto3xk28Cls130 provenance
has publication info: NP68657.RAZY- 5QlkIWgvmFEDFGrw57nFh4yO2Wlvkto3xk28Cls130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68657.RAZY- 5QlkIWgvmFEDFGrw57nFh4yO2Wlvkto3xk28Cls130 assertion
type: Assertion
description: [Genetic variations in ATP2B1, CSK, ARSG and CSMD1 loci are related to blood pressure and/or hypertension in two Korean cohorts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19960030
was generated by: ECO_0000203

NP68669.RAeJ5rcu-oehahTDU877c3lYuTA9oH6kTqZ1A5IsTasVg
has assertion: NP68669.RAeJ5rcu-oehahTDU877c3lYuTA9oH6kTqZ1A5IsTasVg130 assertion
has provenance: NP68669.RAeJ5rcu-oehahTDU877c3lYuTA9oH6kTqZ1A5IsTasVg130 provenance
has publication info: NP68669.RAeJ5rcu-oehahTDU877c3lYuTA9oH6kTqZ1A5IsTasVg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68669.RAeJ5rcu-oehahTDU877c3lYuTA9oH6kTqZ1A5IsTasVg130 assertion
type: Assertion
description: [We observed a strong association between breast cancer occurrence and the genotypes C/C of the RAD51-135G/C polymorphism, Ser/Ser of the OGG1-Ser326Cys and Lys/Gln of the XPD-Lys751Gln, whereas the genotypes G/C of the RAD51-135G/C and Lys/Lys of the XPD-Lys751Gln exerted a protective effect against 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/18977234
was generated by: ECO_0000203

NP68670.RASVNl6JCk2AOuNsDsDygGLfYJv5oF8AdzvyZltO HzDI
has assertion: NP68670.RASVNl6JCk2AOuNsDsDygGLfYJv5oF8AdzvyZltO HzDI130 assertion
has provenance: NP68670.RASVNl6JCk2AOuNsDsDygGLfYJv5oF8AdzvyZltO HzDI130 provenance
has publication info: NP68670.RASVNl6JCk2AOuNsDsDygGLfYJv5oF8AdzvyZltO HzDI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68670.RASVNl6JCk2AOuNsDsDygGLfYJv5oF8AdzvyZltO HzDI130 assertion
type: Assertion
description: [Comprehensive screen of genetic variation in DNA repair pathway genes and postmenopausal 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/20496165
was generated by: ECO_0000203

NP68674.RAbE-0QHQm8DmqnGgGRsHlKvYSfqaapi7-zA5 qcZkNSA
has assertion: NP68674.RAbE-0QHQm8DmqnGgGRsHlKvYSfqaapi7-zA5 qcZkNSA130 assertion
has provenance: NP68674.RAbE-0QHQm8DmqnGgGRsHlKvYSfqaapi7-zA5 qcZkNSA130 provenance
has publication info: NP68674.RAbE-0QHQm8DmqnGgGRsHlKvYSfqaapi7-zA5 qcZkNSA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68674.RAbE-0QHQm8DmqnGgGRsHlKvYSfqaapi7-zA5 qcZkNSA130 assertion
type: Assertion
description: [, our data suggest that Thai women with a certain XRCC1 diplotype or homozygous for two or three variant alleles of XRCC1, OGG1, and APEX1 are likely to have an increased susceptibility to 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/17922186
was generated by: ECO_0000203

NP68678.RAUGfq6APn hpxVd2kiEJ5cTknHS4c1TTiqZ4zhPk8oTM
has assertion: NP68678.RAUGfq6APn hpxVd2kiEJ5cTknHS4c1TTiqZ4zhPk8oTM130 assertion
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has publication info: NP68678.RAUGfq6APn hpxVd2kiEJ5cTknHS4c1TTiqZ4zhPk8oTM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68678.RAUGfq6APn hpxVd2kiEJ5cTknHS4c1TTiqZ4zhPk8oTM130 assertion
type: Assertion
description: [, the variant 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/20562008
was generated by: ECO_0000203

NP68682.RAQAh7AWznVZUDpFkmDAdIa7Rfh4GcPjrnV11PmtwhYMs
has assertion: NP68682.RAQAh7AWznVZUDpFkmDAdIa7Rfh4GcPjrnV11PmtwhYMs130 assertion
has provenance: NP68682.RAQAh7AWznVZUDpFkmDAdIa7Rfh4GcPjrnV11PmtwhYMs130 provenance
has publication info: NP68682.RAQAh7AWznVZUDpFkmDAdIa7Rfh4GcPjrnV11PmtwhYMs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68682.RAQAh7AWznVZUDpFkmDAdIa7Rfh4GcPjrnV11PmtwhYMs130 assertion
type: Assertion
description: [Genetic polymorphism in ornithine decarboxylase and 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/19225907
was generated by: ECO_0000203

NP68684.RARaMKGcK13xAyjyxWKNEnI5RFXsw2qT3iiWtLhBfrJAE
has assertion: NP68684.RARaMKGcK13xAyjyxWKNEnI5RFXsw2qT3iiWtLhBfrJAE130 assertion
has provenance: NP68684.RARaMKGcK13xAyjyxWKNEnI5RFXsw2qT3iiWtLhBfrJAE130 provenance
has publication info: NP68684.RARaMKGcK13xAyjyxWKNEnI5RFXsw2qT3iiWtLhBfrJAE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
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version: v2.1.0.0

NP68684.RARaMKGcK13xAyjyxWKNEnI5RFXsw2qT3iiWtLhBfrJAE130 assertion
type: Assertion
description: [Variants of the melanocortin 1 receptor gene (MC1R) and P gene as indicators of the population origin of an individual.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18839200
was generated by: ECO_0000203

NP68692.RAXNCuZYv6WBdeJog4mMHj4nwUnXckXIZ1rGUtnlnyAoc
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68692.RAXNCuZYv6WBdeJog4mMHj4nwUnXckXIZ1rGUtnlnyAoc130 assertion
type: Assertion
description: [This study supports an underlying polygenic response to interferon beta treatment in MS and highlights the importance of the glutamatergic system in patient response to interferon beta 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/19667218
was generated by: ECO_0000203

NP68694.RAXeumockyobB3NPsxpgDXJi5kIFn79L4VMMY0nDARj-U
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP68694.RAXeumockyobB3NPsxpgDXJi5kIFn79L4VMMY0nDARj-U130 assertion
type: Assertion
description: [A pharmacogenetic study of polymorphisms in interferon pathway genes and response to interferon-alpha treatment in chronic hepatitis B 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/19559055
was generated by: ECO_0000203

NP68700.RAU1jeENRarsKXXTw3RUO6VlCAumkdK2N4Ejsc-4xPKtM
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type: Nanopublication
created: 2014-10-02T12:32:32+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68700.RAU1jeENRarsKXXTw3RUO6VlCAumkdK2N4Ejsc-4xPKtM130 assertion
type: Assertion
description: [These novel genetic findings provide new insights in relation to the mechanisms that might be involved in the development of vitiligo vulgaris.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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was generated by: ECO_0000203

NP68708.RAdPP3 Zi487EbuDKLLyldOI657yLUGVfrq7VwG-RliU0
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP68708.RAdPP3 Zi487EbuDKLLyldOI657yLUGVfrq7VwG-RliU0130 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.
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SIO_000772: http://identifiers.org/pubmed/18676680
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NP68717.RAZn-54MHpwY4M86nNdwJIaO-Z JINa1-nx9XjNS15Its
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP68717.RAZn-54MHpwY4M86nNdwJIaO-Z JINa1-nx9XjNS15Its130 assertion
type: Assertion
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evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19344762
was generated by: ECO_0000203

NP68719.RAZHIqsVs3v5t8k7qpa7ncut3oAXuilNfn I82-iiH-ZU
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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version: v2.1.0.0

NP68719.RAZHIqsVs3v5t8k7qpa7ncut3oAXuilNfn I82-iiH-ZU130 assertion
type: Assertion
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SIO_000772: http://identifiers.org/pubmed/20379614
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NP68722.RAbtoXM3HpLwoZC9HMKPI5HSZ5hyOLi1Zx-WhWvfHjniw
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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NP68722.RAbtoXM3HpLwoZC9HMKPI5HSZ5hyOLi1Zx-WhWvfHjniw130 assertion
type: Assertion
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SIO_000772: http://identifiers.org/pubmed/19488044
was generated by: ECO_0000203

NP68726.RAZNInTjtGkfySA5uMAVCimQvG sHXi1SHu sL1dPwfXU
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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version: v2.1.0.0

NP68726.RAZNInTjtGkfySA5uMAVCimQvG sHXi1SHu sL1dPwfXU130 assertion
type: Assertion
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SIO_000772: http://identifiers.org/pubmed/19548263
was generated by: ECO_0000203

NP68727.RAZWNLLfZ zkmRv9ZYZD48JbEgkebyDO84Q2cPexLCutI
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP68727.RAZWNLLfZ zkmRv9ZYZD48JbEgkebyDO84Q2cPexLCutI130 assertion
type: Assertion
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SIO_000772: http://identifiers.org/pubmed/20014955
was generated by: ECO_0000203

NP68729.RAQI0WU1aDselPf8pj3a6zDg5wF54E4AlrjqpxXnu3gPs
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP68729.RAQI0WU1aDselPf8pj3a6zDg5wF54E4AlrjqpxXnu3gPs130 assertion
type: Assertion
description: [SNPs in neurotrophin system genes and Alzheimer's disease in an Italian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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SIO_000772: http://identifiers.org/pubmed/18780967
was generated by: ECO_0000203

NP68732.RAcsEsmEx vp2CGNtYVeaKhAdWyvL3nq -sMGE7uMgHoU
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type: Nanopublication
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version: v2.1.0.0

NP68732.RAcsEsmEx vp2CGNtYVeaKhAdWyvL3nq -sMGE7uMgHoU130 assertion
type: Assertion
description: [NTRK1 c.1810C>T polymorphism appears to be a new independent prognostic factor of poor outcome in neuroblastoma, especially in children under 18 months of age with no MYCN amplification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20003389
was generated by: ECO_0000203

NP68733.RAS17DPiB Z-2VO63TcWBMShGX86UkLqWszkQlLE95zTk
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP68733.RAS17DPiB Z-2VO63TcWBMShGX86UkLqWszkQlLE95zTk130 assertion
type: Assertion
description: [Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger 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/19598235
was generated by: ECO_0000203

NP68734.RAYUA97OSH5L FqZQRlFpeTZnfMf UYQb538UUDWlNsg
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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NP68734.RAYUA97OSH5L FqZQRlFpeTZnfMf UYQb538UUDWlNsg130 assertion
type: Assertion
description: [Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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SIO_000772: http://identifiers.org/pubmed/19536092
was generated by: ECO_0000203

NP68742.RAZX16nzXWGhk22wCykwT5Af8lkxf3f4cJsEzdzWk3Qtg
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP68742.RAZX16nzXWGhk22wCykwT5Af8lkxf3f4cJsEzdzWk3Qtg130 assertion
type: Assertion
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SIO_000772: http://identifiers.org/pubmed/19197363
was generated by: ECO_0000203

NP68756.RAUC57r1HvVUNWFD6O64pOin9EXEpENcfeifBcjuozCHk
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP68756.RAUC57r1HvVUNWFD6O64pOin9EXEpENcfeifBcjuozCHk130 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.
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SIO_000772: http://identifiers.org/pubmed/19851445
was generated by: ECO_0000203

NP68760.RAb4xiQ6jZ7lOV SmLTEst 0pQQuhzgdQUHxMc-E iO78
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68760.RAb4xiQ6jZ7lOV SmLTEst 0pQQuhzgdQUHxMc-E iO78130 assertion
type: Assertion
description: [Association between sodium- and potassium-activated adenosine triphosphatase alpha isoforms and bipolar 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/19058785
was generated by: ECO_0000203

NP68766.RATrmBrIBJVqBIyHOv7L-CBIIdZ8IqjY31t7J20DyLS5c
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68766.RATrmBrIBJVqBIyHOv7L-CBIIdZ8IqjY31t7J20DyLS5c130 assertion
type: Assertion
description: [NRG1 gene in recurrent major depression: no association in a large-scale case-control 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/19367584
was generated by: ECO_0000203

NP68768.RAeRsqDLi1yuME8 MUjqOE1rAgKg4vH7hUlzBNR-b7mLo
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type: Nanopublication
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rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68768.RAeRsqDLi1yuME8 MUjqOE1rAgKg4vH7hUlzBNR-b7mLo130 assertion
type: Assertion
description: [Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger 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/19598235
was generated by: ECO_0000203

NP68775.RAdidJYjye2qde0HsHVmR9jVNhyS45lxq9dH5iBbS8EBw
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type: Nanopublication
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rights holder: IBIGroup
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NP68775.RAdidJYjye2qde0HsHVmR9jVNhyS45lxq9dH5iBbS8EBw130 assertion
type: Assertion
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SIO_000772: http://identifiers.org/pubmed/18615679
was generated by: ECO_0000203

NP68777.RAXZfR167s9c8qot QOTWETTr3gK4- KnHWs5zdwZfd4E
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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NP68777.RAXZfR167s9c8qot QOTWETTr3gK4- KnHWs5zdwZfd4E130 assertion
type: Assertion
description: [Genetic mutations associated with cigarette smoking in pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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was generated by: ECO_0000203

NP68786.RAV5Rbl3jF2SS7UsMOvi7 0Uf0-y3pGJKx6rwy01U7k0E
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type: Nanopublication
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version: v2.1.0.0

NP68786.RAV5Rbl3jF2SS7UsMOvi7 0Uf0-y3pGJKx6rwy01U7k0E130 assertion
type: Assertion
description: [Screening of 214 single nucleotide polymorphisms in 44 candidate cancer susceptibility genes: a case-control study on gastric and colorectal cancers in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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was generated by: ECO_0000203

NP68788.RAd1I8Y-fQkDB7Mu44qRyPIsHBy2v5u8de35r9DApl2Es
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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NP68788.RAd1I8Y-fQkDB7Mu44qRyPIsHBy2v5u8de35r9DApl2Es130 assertion
type: Assertion
description: [Association of HPA axis genes with suicidal behaviour in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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was generated by: ECO_0000203

NP68793.RAd2nvHdGLyWJcjjDtHIWqs9gsEhKhbDBpLZX06ORPim4
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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NP68793.RAd2nvHdGLyWJcjjDtHIWqs9gsEhKhbDBpLZX06ORPim4130 assertion
type: Assertion
description: [Polymorphisms of the glucocorticoid receptor gene and major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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SIO_000772: http://identifiers.org/pubmed/16580345
was generated by: ECO_0000203

NP68795.RAWbvzkQ4R5mU-WE3Ys6UG8ccFvSbhc-ssa8DKZF gyVI
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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version: v2.1.0.0

NP68795.RAWbvzkQ4R5mU-WE3Ys6UG8ccFvSbhc-ssa8DKZF gyVI130 assertion
type: Assertion
description: [Mutation screen and association analysis of the glucocorticoid receptor gene (NR3C1) in childhood-onset mood disorders (COMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19089807
was generated by: ECO_0000203

NP68796.RAS0PxJjvMSul2jeYyPsV8Vk6Sacn-nKVD7hWydz9Iqsc
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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version: v2.1.0.0

NP68796.RAS0PxJjvMSul2jeYyPsV8Vk6Sacn-nKVD7hWydz9Iqsc130 assertion
type: Assertion
description: [Functional glucocorticoid receptor gene variants do not underlie the high variability of 17-hydroxyprogesterone screening values in healthy newborns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19174530
was generated by: ECO_0000203

NP68802.RAWim uUK EhXFl20w-OR vT50bTcxQi6PQZo3sy9cL9w
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
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version: v2.1.0.0

NP68802.RAWim uUK EhXFl20w-OR vT50bTcxQi6PQZo3sy9cL9w130 assertion
type: Assertion
description: [Glucocorticoid replacement therapy and pharmacogenetics in Addison's disease: effects on bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19282465
was generated by: ECO_0000203

NP68805.RAdLVr2p3NFFOHM9Jjpnl4JIdoMUjqHMdSgv1-5lik6xE
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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version: v2.1.0.0

NP68805.RAdLVr2p3NFFOHM9Jjpnl4JIdoMUjqHMdSgv1-5lik6xE130 assertion
type: Assertion
description: [Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19578796
was generated by: ECO_0000203

NP68809.RAU8ghmWU4M-z7O7r7wSsEwgecshNaiJv9O3B3qSVEhts
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type: Nanopublication
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rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68809.RAU8ghmWU4M-z7O7r7wSsEwgecshNaiJv9O3B3qSVEhts130 assertion
type: Assertion
description: [The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17982421
was generated by: ECO_0000203

NP68813.RAXmxvYD2UUbVWq077aKGfVon1e17BS7KLb1N5Bg-MEHQ
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68813.RAXmxvYD2UUbVWq077aKGfVon1e17BS7KLb1N5Bg-MEHQ130 assertion
type: Assertion
description: [Clinical implications of CYP2D6 genotypes predictive of tamoxifen pharmacokinetics in metastatic breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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was generated by: ECO_0000203

NP68819.RASE6SPtxFTrU6kY22HFVocT0JNlIfq scst2Wa-C4GlE
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68819.RASE6SPtxFTrU6kY22HFVocT0JNlIfq scst2Wa-C4GlE130 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.
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was generated by: ECO_0000203

NP68820.RAdAanQLSu0cPuW3rc59-V2pD9LCVn9ddGp6Gzy51yHzI
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68820.RAdAanQLSu0cPuW3rc59-V2pD9LCVn9ddGp6Gzy51yHzI130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP68821.RARfAhEjm9REUS2vCVKBnXG1XZdQjDP0s24 cCWoeET5Y
has assertion: NP68821.RARfAhEjm9REUS2vCVKBnXG1XZdQjDP0s24 cCWoeET5Y130 assertion
has provenance: NP68821.RARfAhEjm9REUS2vCVKBnXG1XZdQjDP0s24 cCWoeET5Y130 provenance
has publication info: NP68821.RARfAhEjm9REUS2vCVKBnXG1XZdQjDP0s24 cCWoeET5Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68821.RARfAhEjm9REUS2vCVKBnXG1XZdQjDP0s24 cCWoeET5Y130 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

NP68823.RATqIr1Obw6daymlKOS9-9C6tJF2CdueAMjGSXCFvMle0
has assertion: NP68823.RATqIr1Obw6daymlKOS9-9C6tJF2CdueAMjGSXCFvMle0130 assertion
has provenance: NP68823.RATqIr1Obw6daymlKOS9-9C6tJF2CdueAMjGSXCFvMle0130 provenance
has publication info: NP68823.RATqIr1Obw6daymlKOS9-9C6tJF2CdueAMjGSXCFvMle0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68823.RATqIr1Obw6daymlKOS9-9C6tJF2CdueAMjGSXCFvMle0130 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

NP68830.RAa00cwuGcpmhxkkn29Jo4MmU4ofwqaIjmgmX7r4mq sI
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68830.RAa00cwuGcpmhxkkn29Jo4MmU4ofwqaIjmgmX7r4mq sI130 assertion
type: Assertion
description: [PER2 variantion is associated with depression vulnerability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19693801
was generated by: ECO_0000203

NP68831.RAaRkPtzaSNqL6sReQVCZVa R16cOQ7uoQqer5ePz5aJ0
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68831.RAaRkPtzaSNqL6sReQVCZVa R16cOQ7uoQqer5ePz5aJ0130 assertion
type: Assertion
description: [The aim of our study was to investigate the association between REV-ERBalpha gene (NR1D1) single nucleotide polymorphisms (SNPs) and bipolar disorder (BP) in a case-control sample of Sardinian ancestry and evaluate its effect on age at onset (AAO) of BP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19267705
was generated by: ECO_0000203

NP68833.RAQ7NJmoFdvBtEpBjCxihYSCpIvplVRIMwLr-JqN1NI1M
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has publication info: NP68833.RAQ7NJmoFdvBtEpBjCxihYSCpIvplVRIMwLr-JqN1NI1M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68833.RAQ7NJmoFdvBtEpBjCxihYSCpIvplVRIMwLr-JqN1NI1M130 assertion
type: Assertion
description: [Nuclear receptor rev-erb-{alpha} circadian gene variants and lithium carbonate prophylaxis in bipolar affective 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/20348464
was generated by: ECO_0000203

NP68836.RAS5vhvcBaG-xsscBxrMSz42FO 4F4fpAc5cxTqCyRt3Q
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has provenance: NP68836.RAS5vhvcBaG-xsscBxrMSz42FO 4F4fpAc5cxTqCyRt3Q130 provenance
has publication info: NP68836.RAS5vhvcBaG-xsscBxrMSz42FO 4F4fpAc5cxTqCyRt3Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68836.RAS5vhvcBaG-xsscBxrMSz42FO 4F4fpAc5cxTqCyRt3Q130 assertion
type: Assertion
description: [Association analysis of nuclear receptor Rev-erb alpha gene (NR1D1) with mood disorders 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/18804497
was generated by: ECO_0000203

NP68849.RAaTbm0f9j-hI4lp1aymoP477KQkUZ rMBPfX5LUy3F1k
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has publication info: NP68849.RAaTbm0f9j-hI4lp1aymoP477KQkUZ rMBPfX5LUy3F1k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68849.RAaTbm0f9j-hI4lp1aymoP477KQkUZ rMBPfX5LUy3F1k130 assertion
type: Assertion
description: [Tagging single nucleotide polymorphisms in phosphoinositide-3-kinase-related protein kinase genes involved in DNA damage `checkpoints` and lung 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/18451257
was generated by: ECO_0000203

NP68856.RAeURblvX-gJpYPUdh5MN1ii7vV0vCAJvA5ORRYoc3b o
has assertion: NP68856.RAeURblvX-gJpYPUdh5MN1ii7vV0vCAJvA5ORRYoc3b o130 assertion
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has publication info: NP68856.RAeURblvX-gJpYPUdh5MN1ii7vV0vCAJvA5ORRYoc3b o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68856.RAeURblvX-gJpYPUdh5MN1ii7vV0vCAJvA5ORRYoc3b o130 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

NP68859.RAVcq34bfoFXLDhhHfSutHsl-gBXnlj VnaiAyR4T2i68
has assertion: NP68859.RAVcq34bfoFXLDhhHfSutHsl-gBXnlj VnaiAyR4T2i68130 assertion
has provenance: NP68859.RAVcq34bfoFXLDhhHfSutHsl-gBXnlj VnaiAyR4T2i68130 provenance
has publication info: NP68859.RAVcq34bfoFXLDhhHfSutHsl-gBXnlj VnaiAyR4T2i68130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68859.RAVcq34bfoFXLDhhHfSutHsl-gBXnlj VnaiAyR4T2i68130 assertion
type: Assertion
description: [Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic 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/19074885
was generated by: ECO_0000203

NP68864.RAfc7Tj06fdiWxZzrjlFNU2cXcB32A3tGSDKVylq16DvE
has assertion: NP68864.RAfc7Tj06fdiWxZzrjlFNU2cXcB32A3tGSDKVylq16DvE130 assertion
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68864.RAfc7Tj06fdiWxZzrjlFNU2cXcB32A3tGSDKVylq16DvE130 assertion
type: Assertion
description: [A field synopsis on low-penetrance variants in DNA repair genes and 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/19116388
was generated by: ECO_0000203

NP68865.RASnKZydvIZUhF4Y 8IZHnErX8AN 1kh4lcUY89aNJIq4
has assertion: NP68865.RASnKZydvIZUhF4Y 8IZHnErX8AN 1kh4lcUY89aNJIq4130 assertion
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68865.RASnKZydvIZUhF4Y 8IZHnErX8AN 1kh4lcUY89aNJIq4130 assertion
type: Assertion
description: [Description and validation of high-throughput simultaneous genotyping and mutation scanning by high-resolution melting curve 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/19347964
was generated by: ECO_0000203

NP68873.RAWHjC4f tRLtO2qAZzj7JElme09B67Fl-mkFaFqh83yw
has assertion: NP68873.RAWHjC4f tRLtO2qAZzj7JElme09B67Fl-mkFaFqh83yw130 assertion
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has publication info: NP68873.RAWHjC4f tRLtO2qAZzj7JElme09B67Fl-mkFaFqh83yw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68873.RAWHjC4f tRLtO2qAZzj7JElme09B67Fl-mkFaFqh83yw130 assertion
type: Assertion
description: [Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass grafting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19326473
was generated by: ECO_0000203

NP68879.RAQcwe6FqUvVRji79PZ2PPEo6QT904lplbyLOtoGM0lo8
has assertion: NP68879.RAQcwe6FqUvVRji79PZ2PPEo6QT904lplbyLOtoGM0lo8130 assertion
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has publication info: NP68879.RAQcwe6FqUvVRji79PZ2PPEo6QT904lplbyLOtoGM0lo8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68879.RAQcwe6FqUvVRji79PZ2PPEo6QT904lplbyLOtoGM0lo8130 assertion
type: Assertion
description: [Our study indicates interesting new candidate genes and functional pathways for further study and confirms earlier 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/19161160
was generated by: ECO_0000203

NP68880.RASKL2ZcDptRCRw8cT896OL41ItfOuz7VqBhcQXLmU4qc
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68880.RASKL2ZcDptRCRw8cT896OL41ItfOuz7VqBhcQXLmU4qc130 assertion
type: Assertion
description: [We hypothesized that the corin I555(P568) allele would be associated with adverse outcomes and impaired BNP processing in blacks with systolic 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/19919978
was generated by: ECO_0000203

NP68882.RAfx1fMpt VSKzLat7lxr8GojchhVH70xlH58FfOnxioo
has assertion: NP68882.RAfx1fMpt VSKzLat7lxr8GojchhVH70xlH58FfOnxioo130 assertion
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has publication info: NP68882.RAfx1fMpt VSKzLat7lxr8GojchhVH70xlH58FfOnxioo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68882.RAfx1fMpt VSKzLat7lxr8GojchhVH70xlH58FfOnxioo130 assertion
type: Assertion
description: [Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass grafting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19326473
was generated by: ECO_0000203

NP68883.RAeKIsCO M ZtT4vZzmc3XdbsHb8m6CVUKZfAlrlJSFCk
has assertion: NP68883.RAeKIsCO M ZtT4vZzmc3XdbsHb8m6CVUKZfAlrlJSFCk130 assertion
has provenance: NP68883.RAeKIsCO M ZtT4vZzmc3XdbsHb8m6CVUKZfAlrlJSFCk130 provenance
has publication info: NP68883.RAeKIsCO M ZtT4vZzmc3XdbsHb8m6CVUKZfAlrlJSFCk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68883.RAeKIsCO M ZtT4vZzmc3XdbsHb8m6CVUKZfAlrlJSFCk130 assertion
type: Assertion
description: [The genomic basis of cerebral palsy: a HuGE systematic literature 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/19238444
was generated by: ECO_0000203

NP68886.RAZiT-bHH3G76VbG9zWmZgYOeDkqeXKazCu4l8cnbaFz4
has assertion: NP68886.RAZiT-bHH3G76VbG9zWmZgYOeDkqeXKazCu4l8cnbaFz4130 assertion
has provenance: NP68886.RAZiT-bHH3G76VbG9zWmZgYOeDkqeXKazCu4l8cnbaFz4130 provenance
has publication info: NP68886.RAZiT-bHH3G76VbG9zWmZgYOeDkqeXKazCu4l8cnbaFz4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68886.RAZiT-bHH3G76VbG9zWmZgYOeDkqeXKazCu4l8cnbaFz4130 assertion
type: Assertion
description: [Determination of NPM1 mutation status has become essential for the molecular classification of acute myeloid leukemias (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20616361
was generated by: ECO_0000203

NP68894.RAbnwtDzC0lMjpD0-x4oVP75kRxyVJM3chRYcFS5EnVxg
has assertion: NP68894.RAbnwtDzC0lMjpD0-x4oVP75kRxyVJM3chRYcFS5EnVxg130 assertion
has provenance: NP68894.RAbnwtDzC0lMjpD0-x4oVP75kRxyVJM3chRYcFS5EnVxg130 provenance
has publication info: NP68894.RAbnwtDzC0lMjpD0-x4oVP75kRxyVJM3chRYcFS5EnVxg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68894.RAbnwtDzC0lMjpD0-x4oVP75kRxyVJM3chRYcFS5EnVxg130 assertion
type: Assertion
description: [Nucleophosmin (NPM1) mutations occur frequently in adult cytogenetically normal acute myeloid leukemia (CN-AML) and confer favorable 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/19020547
was generated by: ECO_0000203

NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K- m7Ok
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has publication info: NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K- m7Ok130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K- m7Ok130 assertion
type: Assertion
description: [To investigate the association of the polymorphism of NPHS1, coding gene of nephrin, with the degree of proteinuria, renal function, and prognosis of IgA nephropathy (IgAN) in patients in north 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/19671286
was generated by: ECO_0000203

NP68899.RAV7pw4Ibo0PmjSOghF6H39e7WOcZw8HD783msFTKQuK0
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP68899.RAV7pw4Ibo0PmjSOghF6H39e7WOcZw8HD783msFTKQuK0130 assertion
type: Assertion
description: [In two large, independent populations, ABO blood type was statistically significantly associated with the 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/19276450
was generated by: ECO_0000203

NP68901.RAVFWp4x93vneJCIiJ9MGRKKDmy3ZP7-1hR88vA-wo1oo
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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

NP68901.RAVFWp4x93vneJCIiJ9MGRKKDmy3ZP7-1hR88vA-wo1oo130 assertion
type: Assertion
description: [The g.-762T>C polymorphism of the NPC1L1 gene is common in Chinese and contributes to a higher promoter activity and higher serum cholesterol 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/19265861
was generated by: ECO_0000203

NP68904.RAUiV8QywzKpDYHArwSsa6K1epQ6xbw8ZKBHm6O6rwGFY
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has publication info: NP68904.RAUiV8QywzKpDYHArwSsa6K1epQ6xbw8ZKBHm6O6rwGFY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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

NP68904.RAUiV8QywzKpDYHArwSsa6K1epQ6xbw8ZKBHm6O6rwGFY130 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

NP68909.RAbOqwJ3lA35PcTJrTme nuv2Cic13lsCaN9lWBpAE-ak
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has publication info: NP68909.RAbOqwJ3lA35PcTJrTme nuv2Cic13lsCaN9lWBpAE-ak130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68909.RAbOqwJ3lA35PcTJrTme nuv2Cic13lsCaN9lWBpAE-ak130 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

NP68921.RAcms1h7Xvb9ZvKd4bh8NXmhkFokMjdB9VNBBD-WGA64o
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68921.RAcms1h7Xvb9ZvKd4bh8NXmhkFokMjdB9VNBBD-WGA64o130 assertion
type: Assertion
description: [Our finding may contribute to understanding of the pathophysiology of AIP as well as to a priori identification of patients vulnerable for development of AIP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19680635
was generated by: ECO_0000203

NP68929.RAWpA0cjYpzGsLLC5LxVIuBPvFZxSwsTpSjkIrJ6BoFLI
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has provenance: NP68929.RAWpA0cjYpzGsLLC5LxVIuBPvFZxSwsTpSjkIrJ6BoFLI130 provenance
has publication info: NP68929.RAWpA0cjYpzGsLLC5LxVIuBPvFZxSwsTpSjkIrJ6BoFLI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68929.RAWpA0cjYpzGsLLC5LxVIuBPvFZxSwsTpSjkIrJ6BoFLI130 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

NP68933.RAZeVUxBJH98vjAsiBZFuoZwhiRMOVlnQMGFxhBVRojys
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has publication info: NP68933.RAZeVUxBJH98vjAsiBZFuoZwhiRMOVlnQMGFxhBVRojys130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68933.RAZeVUxBJH98vjAsiBZFuoZwhiRMOVlnQMGFxhBVRojys130 assertion
type: Assertion
description: [Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A 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/19794065
was generated by: ECO_0000203

NP68935.RAWS9xSUAnSM-GZbjpT5gvc6jdMGun-O0Y4aftLuf BLQ
has assertion: NP68935.RAWS9xSUAnSM-GZbjpT5gvc6jdMGun-O0Y4aftLuf BLQ130 assertion
has provenance: NP68935.RAWS9xSUAnSM-GZbjpT5gvc6jdMGun-O0Y4aftLuf BLQ130 provenance
has publication info: NP68935.RAWS9xSUAnSM-GZbjpT5gvc6jdMGun-O0Y4aftLuf BLQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68935.RAWS9xSUAnSM-GZbjpT5gvc6jdMGun-O0Y4aftLuf BLQ130 assertion
type: Assertion
description: [Metabolic markers, but not genotyping for 20 diabetogenic SNPs, improve discrimination of incident type 2 diabetes beyond lifestyle 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/19720844
was generated by: ECO_0000203

NP68937.RAfUlqDMGPz0-P1XKdIB7df4LsvoyOWxq0BFnDF9c0AXg
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68937.RAfUlqDMGPz0-P1XKdIB7df4LsvoyOWxq0BFnDF9c0AXg130 assertion
type: Assertion
description: [NOTCH2 mutations in marginal zone 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/18508802
was generated by: ECO_0000203

NP68947.RAV5mXvVIkkE EUSPOkEtex2xCzkkAsWuX70GPdg2npBo
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has publication info: NP68947.RAV5mXvVIkkE EUSPOkEtex2xCzkkAsWuX70GPdg2npBo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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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

NP68947.RAV5mXvVIkkE EUSPOkEtex2xCzkkAsWuX70GPdg2npBo130 assertion
type: Assertion
description: [Role of nitric oxide synthase gene intron 4 and exon 7 polymorphisms in obstructive sleep apnea 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/18651156
was generated by: ECO_0000203

NP68954.RAQQyAfU5iNcqTDnPm6La6rC6 TZY MxKcVvckeT8zZco
has assertion: NP68954.RAQQyAfU5iNcqTDnPm6La6rC6 TZY MxKcVvckeT8zZco130 assertion
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has publication info: NP68954.RAQQyAfU5iNcqTDnPm6La6rC6 TZY MxKcVvckeT8zZco130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68954.RAQQyAfU5iNcqTDnPm6La6rC6 TZY MxKcVvckeT8zZco130 assertion
type: Assertion
description: [Common 894G>T single nucleotide polymorphism in the gene coding for endothelial nitric oxide synthase (eNOS) and risk of congenital heart 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/18844489
was generated by: ECO_0000203

NP68955.RAXCxHxkSVpd6ZtSpB7yhjynfDsAL5bw8sGaGnnkZFFjI
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68955.RAXCxHxkSVpd6ZtSpB7yhjynfDsAL5bw8sGaGnnkZFFjI130 assertion
type: Assertion
description: [The G894T polymorphism of eNOS gene is associated with pulmonary hypertension of COPD 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/18953956
was generated by: ECO_0000203

NP68956.RAadKtv4zlHZGY8AvzysQI9LCRJ0Pbg0jL-3M9NyYMVZI
has assertion: NP68956.RAadKtv4zlHZGY8AvzysQI9LCRJ0Pbg0jL-3M9NyYMVZI130 assertion
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has publication info: NP68956.RAadKtv4zlHZGY8AvzysQI9LCRJ0Pbg0jL-3M9NyYMVZI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68956.RAadKtv4zlHZGY8AvzysQI9LCRJ0Pbg0jL-3M9NyYMVZI130 assertion
type: Assertion
description: [In this COPD cohort we confirm that PH is frequent and usually mild, but out of proportion in a subgroup.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19556740
was generated by: ECO_0000203

NP68970.RAYupx5b93 Iyh WGwGy25ZCVpKeNgnYkKiNDwdoW8PuQ
has assertion: NP68970.RAYupx5b93 Iyh WGwGy25ZCVpKeNgnYkKiNDwdoW8PuQ130 assertion
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68970.RAYupx5b93 Iyh WGwGy25ZCVpKeNgnYkKiNDwdoW8PuQ130 assertion
type: Assertion
description: [The endothelial nitric oxide synthase Glu298Asp polymorphism is not a risk factor for endometriosis in south Indian 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/18313829
was generated by: ECO_0000203

NP68971.RAWpiyIfBB6rXUUjwviI728rtQ6GOl4aXrVCNGfgK1VKc
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP68971.RAWpiyIfBB6rXUUjwviI728rtQ6GOl4aXrVCNGfgK1VKc130 assertion
type: Assertion
description: [Relationships between endothelial nitric oxide synthase gene polymorphisms and osteoporosis 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/19650200
was generated by: ECO_0000203

NP68974.RAb05SPL qpJXIO6-VGS 6w0FliRHKgCoaT-5AeuwZw9E
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68974.RAb05SPL qpJXIO6-VGS 6w0FliRHKgCoaT-5AeuwZw9E130 assertion
type: Assertion
description: [Our findings suggest that there are at least 2 pathways in the pathogenesis of severe 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/19838007
was generated by: ECO_0000203

NP68975.RAfCQn5pcQFXGOcGdbZtOjaNU71IKQY7bx0CEt9uWyk6Q
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
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version: v2.1.0.0

NP68975.RAfCQn5pcQFXGOcGdbZtOjaNU71IKQY7bx0CEt9uWyk6Q130 assertion
type: Assertion
description: [Interactions were observed between NOS3 SNPs and female sex and postmenopausal hormone use in the women in relation to HTPOAG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19815736
was generated by: ECO_0000203

NP68978.RAU4tFwTNBYi85ztaegMUVm1ZT9grs4WTk1CjGWCn8P3I
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68978.RAU4tFwTNBYi85ztaegMUVm1ZT9grs4WTk1CjGWCn8P3I130 assertion
type: Assertion
description: [Endothelial nitric oxide synthase and nicotinamide adenosine dinucleotide phosphate oxidase p22phox gene (C242T) polymorphisms and systemic lupus erythematosus 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/19965945
was generated by: ECO_0000203

NP68986.RAWC-YKxcXYszlorGOxibzBHOsjN8YHczKC64uZN-Vtzc
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP68986.RAWC-YKxcXYszlorGOxibzBHOsjN8YHczKC64uZN-Vtzc130 assertion
type: Assertion
description: [Genetic profiling of genes from the oxidative stress pathway among North and South 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/18720901
was generated by: ECO_0000203

NP68988.RARX2Zi 7iYM2QP mBQHjvSNMWPA9cYjWlfhOqh5SXi4E
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP68988.RARX2Zi 7iYM2QP mBQHjvSNMWPA9cYjWlfhOqh5SXi4E130 assertion
type: Assertion
description: [In this work we investigated about the presence of a correlation between a (CA)n repeat located in exon 29 of NOS1 gene and the beta-thalassemia trait 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/19103196
was generated by: ECO_0000203

NP68993.RActQyJD5zqKw yyyDhXaTVrAmJDmFYoaTI4gCcXEdKn0
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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

NP68993.RActQyJD5zqKw yyyDhXaTVrAmJDmFYoaTI4gCcXEdKn0130 assertion
type: Assertion
description: [Microarray analysis of multiple candidate genes and associated plasma proteins for nephropathy secondary to type 2 diabetes among Chinese 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/19415232
was generated by: ECO_0000203

NP68994.RAV95eXNPlKAyTF8UbcsK6Xnp4b1Sl6VpiGxtawHL--m0
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68994.RAV95eXNPlKAyTF8UbcsK6Xnp4b1Sl6VpiGxtawHL--m0130 assertion
type: Assertion
description: [This study suggests that common genetic variants in the OR10J3 and FCER1A be strongly associated with breast cancer risk among 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/19372141
was generated by: ECO_0000203

NP68996.RAT1vsp6CwbwCN1WNvpqGfQtrttATpvDiP5W4lZvGxf94
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68996.RAT1vsp6CwbwCN1WNvpqGfQtrttATpvDiP5W4lZvGxf94130 assertion
type: Assertion
description: [Identification and association analysis of single nucleotide polymorphisms in the human noggin (NOG) gene and osteoporosis 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/19167531
was generated by: ECO_0000203

NP68999.RAYMlBEtJc5MWCJIlKIt4Ef7G73oIc wf8vz PEdcDGxo
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP68999.RAYMlBEtJc5MWCJIlKIt4Ef7G73oIc wf8vz PEdcDGxo130 assertion
type: Assertion
description: [No association was found between infant NNMT gene variants and risk for spina bifida in our 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/18553462
was generated by: ECO_0000203

NP69006.RAbSsZ7lSkPn4vF2gA00MJOLbK1A5HYtNU6MVKtEBnwq8
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP69006.RAbSsZ7lSkPn4vF2gA00MJOLbK1A5HYtNU6MVKtEBnwq8130 assertion
type: Assertion
description: [Association analysis among polymorphisms of the various genes and chronic alcoholic 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/18336668
was generated by: ECO_0000203

NP69008.RATOvd7PgHt7zl-vlMCR0Bm8PgZnVz5HZqv-WQSI- A-0
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP69008.RATOvd7PgHt7zl-vlMCR0Bm8PgZnVz5HZqv-WQSI- A-0130 assertion
type: Assertion
description: [In this study, we evaluated the risks of OC associated with common germline variants in five oncogenes (BRAF, ERBB2, KRAS, NMI and PIK3CA) known to be involved in OC 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/19240718
was generated by: ECO_0000203

NP69009.RASrm355O 86IAtmIQjW-kKDSing2IgQAulBRR-Eo8qI8
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has publication info: NP69009.RASrm355O 86IAtmIQjW-kKDSing2IgQAulBRR-Eo8qI8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69009.RASrm355O 86IAtmIQjW-kKDSing2IgQAulBRR-Eo8qI8130 assertion
type: Assertion
description: [Variants encoding lower activity of NOS3 may affect outcomes in breast cancer patients, with the direction of risk differing depending on chemotherapy 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/19671875
was generated by: ECO_0000203

NP69014.RAQt75rFG4tuwc3SCl4im9rA83JcqRy5pl7-2d6YZBEEM
has assertion: NP69014.RAQt75rFG4tuwc3SCl4im9rA83JcqRy5pl7-2d6YZBEEM130 assertion
has provenance: NP69014.RAQt75rFG4tuwc3SCl4im9rA83JcqRy5pl7-2d6YZBEEM130 provenance
has publication info: NP69014.RAQt75rFG4tuwc3SCl4im9rA83JcqRy5pl7-2d6YZBEEM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69014.RAQt75rFG4tuwc3SCl4im9rA83JcqRy5pl7-2d6YZBEEM130 assertion
type: Assertion
description: [SNPs located at the gene HUS1 are good candidates for further investigation in independent association studies and functional assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18950845
was generated by: ECO_0000203

NP69015.RAWwCbLmJPvdEzSZ7XPbsrmzjf1MrT5ZAKi4SUI V5oJc
has assertion: NP69015.RAWwCbLmJPvdEzSZ7XPbsrmzjf1MrT5ZAKi4SUI V5oJc130 assertion
has provenance: NP69015.RAWwCbLmJPvdEzSZ7XPbsrmzjf1MrT5ZAKi4SUI V5oJc130 provenance
has publication info: NP69015.RAWwCbLmJPvdEzSZ7XPbsrmzjf1MrT5ZAKi4SUI V5oJc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69015.RAWwCbLmJPvdEzSZ7XPbsrmzjf1MrT5ZAKi4SUI V5oJc130 assertion
type: Assertion
description: [Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot 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/19714462
was generated by: ECO_0000203

NP69023.RAUGz2uuqeWlYCb5K4jX2rRHtRrwDWwyyCIZJ4ISq2K8Q
has assertion: NP69023.RAUGz2uuqeWlYCb5K4jX2rRHtRrwDWwyyCIZJ4ISq2K8Q130 assertion
has provenance: NP69023.RAUGz2uuqeWlYCb5K4jX2rRHtRrwDWwyyCIZJ4ISq2K8Q130 provenance
has publication info: NP69023.RAUGz2uuqeWlYCb5K4jX2rRHtRrwDWwyyCIZJ4ISq2K8Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69023.RAUGz2uuqeWlYCb5K4jX2rRHtRrwDWwyyCIZJ4ISq2K8Q130 assertion
type: Assertion
description: [Increasing evidence suggests a role for nerve growth factor (NGFB), brain-derived neurotrophic factor (BDNF), and their receptors, nerve growth factor receptor (NGFR), and neurotrophin tyrosine kinase receptors 1 and 2 (NTRK1 and NTRK2), 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/18780967
was generated by: ECO_0000203

NP69037.RAeWZUWzpMtDikdXY8ndTp-HVu I4VzNlWkkVW8fVq KU
has assertion: NP69037.RAeWZUWzpMtDikdXY8ndTp-HVu I4VzNlWkkVW8fVq KU130 assertion
has provenance: NP69037.RAeWZUWzpMtDikdXY8ndTp-HVu I4VzNlWkkVW8fVq KU130 provenance
has publication info: NP69037.RAeWZUWzpMtDikdXY8ndTp-HVu I4VzNlWkkVW8fVq KU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69037.RAeWZUWzpMtDikdXY8ndTp-HVu I4VzNlWkkVW8fVq KU130 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

NP69038.RAQMb1B8BZgU68L3DLwxl8DglRnnULOt6b6 WCC0lS1NI
has assertion: NP69038.RAQMb1B8BZgU68L3DLwxl8DglRnnULOt6b6 WCC0lS1NI130 assertion
has provenance: NP69038.RAQMb1B8BZgU68L3DLwxl8DglRnnULOt6b6 WCC0lS1NI130 provenance
has publication info: NP69038.RAQMb1B8BZgU68L3DLwxl8DglRnnULOt6b6 WCC0lS1NI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69038.RAQMb1B8BZgU68L3DLwxl8DglRnnULOt6b6 WCC0lS1NI130 assertion
type: Assertion
description: [SNPs located at the gene HUS1 are good candidates for further investigation in independent association studies and functional assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18950845
was generated by: ECO_0000203

NP69042.RAdbPMbg0- nsZs6zJEb01j3JarxKUf3jKo7ujDg4HbeE
has assertion: NP69042.RAdbPMbg0- nsZs6zJEb01j3JarxKUf3jKo7ujDg4HbeE130 assertion
has provenance: NP69042.RAdbPMbg0- nsZs6zJEb01j3JarxKUf3jKo7ujDg4HbeE130 provenance
has publication info: NP69042.RAdbPMbg0- nsZs6zJEb01j3JarxKUf3jKo7ujDg4HbeE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69042.RAdbPMbg0- nsZs6zJEb01j3JarxKUf3jKo7ujDg4HbeE130 assertion
type: Assertion
description: [Considering the number of single-SNP tests performed and null gene-level results, we conclude that NFKBIA and NFKBIB are not likely to harbor ovarian cancer risk 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/19500386
was generated by: ECO_0000203

NP69044.RAZGoc8LvGHwZcypulucp59FPBggky6dtpx 1r4eMXW8A
has assertion: NP69044.RAZGoc8LvGHwZcypulucp59FPBggky6dtpx 1r4eMXW8A130 assertion
has provenance: NP69044.RAZGoc8LvGHwZcypulucp59FPBggky6dtpx 1r4eMXW8A130 provenance
has publication info: NP69044.RAZGoc8LvGHwZcypulucp59FPBggky6dtpx 1r4eMXW8A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69044.RAZGoc8LvGHwZcypulucp59FPBggky6dtpx 1r4eMXW8A130 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

NP69049.RAeMecCD2WErselwlqeArfEohSNsdRGSFgZgsIGLNk1lc
has assertion: NP69049.RAeMecCD2WErselwlqeArfEohSNsdRGSFgZgsIGLNk1lc130 assertion
has provenance: NP69049.RAeMecCD2WErselwlqeArfEohSNsdRGSFgZgsIGLNk1lc130 provenance
has publication info: NP69049.RAeMecCD2WErselwlqeArfEohSNsdRGSFgZgsIGLNk1lc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69049.RAeMecCD2WErselwlqeArfEohSNsdRGSFgZgsIGLNk1lc130 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

NP69051.RAVXpWWGuLSgeMgErfZcmbBp3jBlMq4fP0NmoKf5GCXwE
has assertion: NP69051.RAVXpWWGuLSgeMgErfZcmbBp3jBlMq4fP0NmoKf5GCXwE130 assertion
has provenance: NP69051.RAVXpWWGuLSgeMgErfZcmbBp3jBlMq4fP0NmoKf5GCXwE130 provenance
has publication info: NP69051.RAVXpWWGuLSgeMgErfZcmbBp3jBlMq4fP0NmoKf5GCXwE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69051.RAVXpWWGuLSgeMgErfZcmbBp3jBlMq4fP0NmoKf5GCXwE130 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

NP69052.RAfJ-6k1Py-oWiGJ00FEBgtCuciRfiFkyQJLgIyPo25qY
has assertion: NP69052.RAfJ-6k1Py-oWiGJ00FEBgtCuciRfiFkyQJLgIyPo25qY130 assertion
has provenance: NP69052.RAfJ-6k1Py-oWiGJ00FEBgtCuciRfiFkyQJLgIyPo25qY130 provenance
has publication info: NP69052.RAfJ-6k1Py-oWiGJ00FEBgtCuciRfiFkyQJLgIyPo25qY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69052.RAfJ-6k1Py-oWiGJ00FEBgtCuciRfiFkyQJLgIyPo25qY130 assertion
type: Assertion
description: [Although the polymorphisms at NFKB1, FAS-1377, and extended haplotype FAS-1377G/-670G may play a role in the development of silicosis in the Chinese population, our findings should be verified by larger studies with >1 case/control ratio.]. 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

NP69054.RAci9mM5hDTeuwiYx9LXd6SKwtfwC4-SKRiXBTwmL3hVs
has assertion: NP69054.RAci9mM5hDTeuwiYx9LXd6SKwtfwC4-SKRiXBTwmL3hVs130 assertion
has provenance: NP69054.RAci9mM5hDTeuwiYx9LXd6SKwtfwC4-SKRiXBTwmL3hVs130 provenance
has publication info: NP69054.RAci9mM5hDTeuwiYx9LXd6SKwtfwC4-SKRiXBTwmL3hVs130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69054.RAci9mM5hDTeuwiYx9LXd6SKwtfwC4-SKRiXBTwmL3hVs130 assertion
type: Assertion
description: [This result may indicate that the effect of interferon-alpha treatment is dependent on the availability of nuclear factor-kappaB and the polymorphism in NFKB1 may, therefore, be a good prognostic marker for multiple myeloma patients on maintenance treatment with interferon-alpha after high-dose 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/19734419
was generated by: ECO_0000203

NP69066.RAbDMgHC363aKcs2n1V sLgIdJQNYWh5ZLVYNRjqFNf9g
has assertion: NP69066.RAbDMgHC363aKcs2n1V sLgIdJQNYWh5ZLVYNRjqFNf9g130 assertion
has provenance: NP69066.RAbDMgHC363aKcs2n1V sLgIdJQNYWh5ZLVYNRjqFNf9g130 provenance
has publication info: NP69066.RAbDMgHC363aKcs2n1V sLgIdJQNYWh5ZLVYNRjqFNf9g130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69066.RAbDMgHC363aKcs2n1V sLgIdJQNYWh5ZLVYNRjqFNf9g130 assertion
type: Assertion
description: [These results suggest that the NFKB1 promoter polymorphism is a useful marker for the identification of patients with superficial bladder cancer where the risk of recurrence is high.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17725175
was generated by: ECO_0000203

NP69069.RAcTraau1LkaghOHoFJlHpuxvW8ZR4KcMjn8dW6I87RWw
has assertion: NP69069.RAcTraau1LkaghOHoFJlHpuxvW8ZR4KcMjn8dW6I87RWw130 assertion
has provenance: NP69069.RAcTraau1LkaghOHoFJlHpuxvW8ZR4KcMjn8dW6I87RWw130 provenance
has publication info: NP69069.RAcTraau1LkaghOHoFJlHpuxvW8ZR4KcMjn8dW6I87RWw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69069.RAcTraau1LkaghOHoFJlHpuxvW8ZR4KcMjn8dW6I87RWw130 assertion
type: Assertion
description: [Since the presence of the rs2304052 C allele is associated with an increased risk (odds ratio: 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/19817957
was generated by: ECO_0000203

NP69074.RASCpVn-cBBkh2auchyb4tStz2FDf6E5Kx2R6ZOUsoSoU
has assertion: NP69074.RASCpVn-cBBkh2auchyb4tStz2FDf6E5Kx2R6ZOUsoSoU130 assertion
has provenance: NP69074.RASCpVn-cBBkh2auchyb4tStz2FDf6E5Kx2R6ZOUsoSoU130 provenance
has publication info: NP69074.RASCpVn-cBBkh2auchyb4tStz2FDf6E5Kx2R6ZOUsoSoU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69074.RASCpVn-cBBkh2auchyb4tStz2FDf6E5Kx2R6ZOUsoSoU130 assertion
type: Assertion
description: [Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21085187
was generated by: ECO_0000203

NP69087.RAWOIaO9cq3OlGMkgWv0ILOCIKVITam3ahDxqcfeeB-2I
has assertion: NP69087.RAWOIaO9cq3OlGMkgWv0ILOCIKVITam3ahDxqcfeeB-2I130 assertion
has provenance: NP69087.RAWOIaO9cq3OlGMkgWv0ILOCIKVITam3ahDxqcfeeB-2I130 provenance
has publication info: NP69087.RAWOIaO9cq3OlGMkgWv0ILOCIKVITam3ahDxqcfeeB-2I130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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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

NP69087.RAWOIaO9cq3OlGMkgWv0ILOCIKVITam3ahDxqcfeeB-2I130 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

NP69090.RATkiyyVtEJuPEyvq0r6gDcegpsctfgQcLmy0zqwiOh4Y
has assertion: NP69090.RATkiyyVtEJuPEyvq0r6gDcegpsctfgQcLmy0zqwiOh4Y130 assertion
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has publication info: NP69090.RATkiyyVtEJuPEyvq0r6gDcegpsctfgQcLmy0zqwiOh4Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69090.RATkiyyVtEJuPEyvq0r6gDcegpsctfgQcLmy0zqwiOh4Y130 assertion
type: Assertion
description: [Centrosome-related genes, genetic variation, and 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/20508983
was generated by: ECO_0000203

NP69093.RAVFHz0PxrCkGcn3DKjq18W zFLfTSiV7HmF6XSWkLY-M
has assertion: NP69093.RAVFHz0PxrCkGcn3DKjq18W zFLfTSiV7HmF6XSWkLY-M130 assertion
has provenance: NP69093.RAVFHz0PxrCkGcn3DKjq18W zFLfTSiV7HmF6XSWkLY-M130 provenance
has publication info: NP69093.RAVFHz0PxrCkGcn3DKjq18W zFLfTSiV7HmF6XSWkLY-M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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authored by: 0000-0002-9383-528X
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69093.RAVFHz0PxrCkGcn3DKjq18W zFLfTSiV7HmF6XSWkLY-M130 assertion
type: Assertion
description: [Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: preliminary evidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19054571
was generated by: ECO_0000203

NP69095.RAcx-UPf6uv00jqMuOuqR5yYbm 0Rbf 5-rWsD7j3UgiU
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP69095.RAcx-UPf6uv00jqMuOuqR5yYbm 0Rbf 5-rWsD7j3UgiU130 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

NP69096.RAUvJvdJR4rU-quWjiVBouxlhZ3 JW9bd4NW6kKs8zjIk
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP69096.RAUvJvdJR4rU-quWjiVBouxlhZ3 JW9bd4NW6kKs8zjIk130 assertion
type: Assertion
description: [Polymorphisms in mitochondrial genes 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/19064571
was generated by: ECO_0000203

NP69101.RAa3lpUHA74 YoXfOx1pXaIePIZy8UYgA0aBknn3E5DBY
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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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version: v2.1.0.0

NP69101.RAa3lpUHA74 YoXfOx1pXaIePIZy8UYgA0aBknn3E5DBY130 assertion
type: Assertion
description: [Polymorphisms in mitochondrial genes 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/19064571
was generated by: ECO_0000203

NP69105.RAYvd5J2FPlWRXx3E77MIVY5u1sIL5RuMrkvNXj5LL-FU
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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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

NP69105.RAYvd5J2FPlWRXx3E77MIVY5u1sIL5RuMrkvNXj5LL-FU130 assertion
type: Assertion
description: [Polymorphisms in mitochondrial genes 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/19064571
was generated by: ECO_0000203

NP69106.RAb8ygBOl9bN6EtSpiadmsNhxI0gOfpq tUft2e1zuRu8
has assertion: NP69106.RAb8ygBOl9bN6EtSpiadmsNhxI0gOfpq tUft2e1zuRu8130 assertion
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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version: v2.1.0.0

NP69106.RAb8ygBOl9bN6EtSpiadmsNhxI0gOfpq tUft2e1zuRu8130 assertion
type: Assertion
description: [Polymorphisms in mitochondrial genes 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/19064571
was generated by: ECO_0000203

NP69109.RAYz0FJKNYE KSwUMg45pwJACAskGTExrZc4poDedaZ2w
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69109.RAYz0FJKNYE KSwUMg45pwJACAskGTExrZc4poDedaZ2w130 assertion
type: Assertion
description: [Short-term exercise training does not stimulate skeletal muscle ATP synthesis in relatives of humans with 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/19265027
was generated by: ECO_0000203

NP69113.RAd mxEKGLDzCqER oDNXKnpUVGJ2JKCK-WgUTxYY21kI
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
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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

NP69113.RAd mxEKGLDzCqER oDNXKnpUVGJ2JKCK-WgUTxYY21kI130 assertion
type: Assertion
description: [Polymorphisms in mitochondrial genes 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/19064571
was generated by: ECO_0000203

NP69116.RAXaJes 83y9QVxa3SgJYVjk9ivrZJhS7 -YJoNYJTTQI
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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version: v2.1.0.0

NP69116.RAXaJes 83y9QVxa3SgJYVjk9ivrZJhS7 -YJoNYJTTQI130 assertion
type: Assertion
description: [SNPs located at the gene HUS1 are good candidates for further investigation in independent association studies and functional assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18950845
was generated by: ECO_0000203

NP69119.RAQMWD50yvH-kkvuhDOzq0IHzmIHKrzB5JjCGm5AoQcMM
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
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

NP69119.RAQMWD50yvH-kkvuhDOzq0IHzmIHKrzB5JjCGm5AoQcMM130 assertion
type: Assertion
description: [Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white 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/19064572
was generated by: ECO_0000203

NP69123.RAcECShmngfL78pKP6XO3u2M8QlixFsbEhOGEl9 6-z s
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP69123.RAcECShmngfL78pKP6XO3u2M8QlixFsbEhOGEl9 6-z s130 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

NP69124.RAf9tbZCqgin3TJxaZDcJSJb9Tq00JsuB3YVYY0kikzBo
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP69124.RAf9tbZCqgin3TJxaZDcJSJb9Tq00JsuB3YVYY0kikzBo130 assertion
type: Assertion
description: [Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white 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/19064572
was generated by: ECO_0000203

NP69129.RASeFDbmcodETrURLcdshIk1C9Gaq7-oq09XDOv0uKsPs
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type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP69129.RASeFDbmcodETrURLcdshIk1C9Gaq7-oq09XDOv0uKsPs130 assertion
type: Assertion
description: [We systematically investigated the association of 48 SNPS in four vitamin D metabolizing genes CYP27A1, GC, CYP27B1 and CYP24A1 with serum 25-hydroxyvitamin D 25(OH)D and 1,25-dihydroxyvitamin D 1,25(OH)(2)D levels and the association of these SNPS and an additional 164 SNPS in eight downstream mediators of vitamin D signaling VDR, RXRA, RXRB, PPAR, NCOA1, NCOA2, NCOA3 and SMAD3 with prostate cancer risk in the 749 incident prostate cancer cases and 781 controls of the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19255064
was generated by: ECO_0000203

NP69135.RAU228Z8eBKr9Mt1V-pgEWFSteAkWZlIHisOL2CmhfyMM
has assertion: NP69135.RAU228Z8eBKr9Mt1V-pgEWFSteAkWZlIHisOL2CmhfyMM130 assertion
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has publication info: NP69135.RAU228Z8eBKr9Mt1V-pgEWFSteAkWZlIHisOL2CmhfyMM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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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

NP69135.RAU228Z8eBKr9Mt1V-pgEWFSteAkWZlIHisOL2CmhfyMM130 assertion
type: Assertion
description: [This study suggests that common genetic variants in the OR10J3 and FCER1A be strongly associated with breast cancer risk among 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/19372141
was generated by: ECO_0000203

NP69136.RAc6TJfbbFQHV55rbOk QqHbXPJkzQQfvz5wD9ZuzfAYE
has assertion: NP69136.RAc6TJfbbFQHV55rbOk QqHbXPJkzQQfvz5wD9ZuzfAYE130 assertion
has provenance: NP69136.RAc6TJfbbFQHV55rbOk QqHbXPJkzQQfvz5wD9ZuzfAYE130 provenance
has publication info: NP69136.RAc6TJfbbFQHV55rbOk QqHbXPJkzQQfvz5wD9ZuzfAYE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69136.RAc6TJfbbFQHV55rbOk QqHbXPJkzQQfvz5wD9ZuzfAYE130 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

NP69140.RAbA-PAjtroQsG8m40Wmng0J0QZZgvL1YCiizBflM5HS8
has assertion: NP69140.RAbA-PAjtroQsG8m40Wmng0J0QZZgvL1YCiizBflM5HS8130 assertion
has provenance: NP69140.RAbA-PAjtroQsG8m40Wmng0J0QZZgvL1YCiizBflM5HS8130 provenance
has publication info: NP69140.RAbA-PAjtroQsG8m40Wmng0J0QZZgvL1YCiizBflM5HS8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69140.RAbA-PAjtroQsG8m40Wmng0J0QZZgvL1YCiizBflM5HS8130 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

NP69146.RAcdBPH7tj6 EZsp8KVT6ioyMjsfEhdVwlryLq50aCAO0
has assertion: NP69146.RAcdBPH7tj6 EZsp8KVT6ioyMjsfEhdVwlryLq50aCAO0130 assertion
has provenance: NP69146.RAcdBPH7tj6 EZsp8KVT6ioyMjsfEhdVwlryLq50aCAO0130 provenance
has publication info: NP69146.RAcdBPH7tj6 EZsp8KVT6ioyMjsfEhdVwlryLq50aCAO0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69146.RAcdBPH7tj6 EZsp8KVT6ioyMjsfEhdVwlryLq50aCAO0130 assertion
type: Assertion
description: [the risk of cervical cancer is increased in passive smokers and in users of oral contraceptives with certain NBS1 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/18949738
was generated by: ECO_0000203

NP69149.RARewl-TiUWIWsVAGrchewXJrE0C5ghbvOfNlwJvZU5vk
has assertion: NP69149.RARewl-TiUWIWsVAGrchewXJrE0C5ghbvOfNlwJvZU5vk130 assertion
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has publication info: NP69149.RARewl-TiUWIWsVAGrchewXJrE0C5ghbvOfNlwJvZU5vk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP69149.RARewl-TiUWIWsVAGrchewXJrE0C5ghbvOfNlwJvZU5vk130 assertion
type: Assertion
description: [Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant 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/18280732
was generated by: ECO_0000203

NP69150.RAdSeo2 ymbs8sg3xQ0c-CXWt4FBOdM6 WOUrrBp74kN4
has assertion: NP69150.RAdSeo2 ymbs8sg3xQ0c-CXWt4FBOdM6 WOUrrBp74kN4130 assertion
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has publication info: NP69150.RAdSeo2 ymbs8sg3xQ0c-CXWt4FBOdM6 WOUrrBp74kN4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69150.RAdSeo2 ymbs8sg3xQ0c-CXWt4FBOdM6 WOUrrBp74kN4130 assertion
type: Assertion
description: [Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic 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/19074885
was generated by: ECO_0000203

NP69158.RAZ30zBDEPecUx9 HmtzNF7frnBwbEVy10qEVUlYYCP2E
has assertion: NP69158.RAZ30zBDEPecUx9 HmtzNF7frnBwbEVy10qEVUlYYCP2E130 assertion
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has publication info: NP69158.RAZ30zBDEPecUx9 HmtzNF7frnBwbEVy10qEVUlYYCP2E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69158.RAZ30zBDEPecUx9 HmtzNF7frnBwbEVy10qEVUlYYCP2E130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP69159.RAew6ct-Tzfuhw1e01zhBX2qUXebPq1By67wDtxXlw9OA
has assertion: NP69159.RAew6ct-Tzfuhw1e01zhBX2qUXebPq1By67wDtxXlw9OA130 assertion
has provenance: NP69159.RAew6ct-Tzfuhw1e01zhBX2qUXebPq1By67wDtxXlw9OA130 provenance
has publication info: NP69159.RAew6ct-Tzfuhw1e01zhBX2qUXebPq1By67wDtxXlw9OA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69159.RAew6ct-Tzfuhw1e01zhBX2qUXebPq1By67wDtxXlw9OA130 assertion
type: Assertion
description: [Association of polymorphisms in genes of the homologous recombination DNA repair pathway and thyroid 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/19772428
was generated by: ECO_0000203

NP69164.RAW7gP 2-5X1EieVjULGRAoJa4B9fppAFafZXwuoFlBww
has assertion: NP69164.RAW7gP 2-5X1EieVjULGRAoJa4B9fppAFafZXwuoFlBww130 assertion
has provenance: NP69164.RAW7gP 2-5X1EieVjULGRAoJa4B9fppAFafZXwuoFlBww130 provenance
has publication info: NP69164.RAW7gP 2-5X1EieVjULGRAoJa4B9fppAFafZXwuoFlBww130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69164.RAW7gP 2-5X1EieVjULGRAoJa4B9fppAFafZXwuoFlBww130 assertion
type: Assertion
description: [Molecular-genetic analysis of natural and stimulated ovulation impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18630123
was generated by: ECO_0000203

NP69168.RAar1tlFeLm5u YSe FfKPNDFs7pCMo55OnkV6EcChlxM
has assertion: NP69168.RAar1tlFeLm5u YSe FfKPNDFs7pCMo55OnkV6EcChlxM130 assertion
has provenance: NP69168.RAar1tlFeLm5u YSe FfKPNDFs7pCMo55OnkV6EcChlxM130 provenance
has publication info: NP69168.RAar1tlFeLm5u YSe FfKPNDFs7pCMo55OnkV6EcChlxM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69168.RAar1tlFeLm5u YSe FfKPNDFs7pCMo55OnkV6EcChlxM130 assertion
type: Assertion
description: [Our study indicates interesting new candidate genes and functional pathways for further study and confirms earlier 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/19161160
was generated by: ECO_0000203

NP69177.RAa jGuPB2J8RrKkX2rmT lXYebURufsQoTcsRliRyru0
has assertion: NP69177.RAa jGuPB2J8RrKkX2rmT lXYebURufsQoTcsRliRyru0130 assertion
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has publication info: NP69177.RAa jGuPB2J8RrKkX2rmT lXYebURufsQoTcsRliRyru0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69177.RAa jGuPB2J8RrKkX2rmT lXYebURufsQoTcsRliRyru0130 assertion
type: Assertion
description: [A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility 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/20972438
was generated by: ECO_0000203

NP69181.RARJzOX-Yaoty8NWB s6LlotdQjKdrWy33HlXOS8jOA5s
has assertion: NP69181.RARJzOX-Yaoty8NWB s6LlotdQjKdrWy33HlXOS8jOA5s130 assertion
has provenance: NP69181.RARJzOX-Yaoty8NWB s6LlotdQjKdrWy33HlXOS8jOA5s130 provenance
has publication info: NP69181.RARJzOX-Yaoty8NWB s6LlotdQjKdrWy33HlXOS8jOA5s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69181.RARJzOX-Yaoty8NWB s6LlotdQjKdrWy33HlXOS8jOA5s130 assertion
type: Assertion
description: [The effect of polymorphism of genes of xenobiotics detoxication on the frequencies of spontaneous and induced chromosome aberrations in human lymphocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19947517
was generated by: ECO_0000203

NP69185.RAdVaF7u21CKir Sytv3gdpBXugpdRa0iHwp2oqXkZcA8
has assertion: NP69185.RAdVaF7u21CKir Sytv3gdpBXugpdRa0iHwp2oqXkZcA8130 assertion
has provenance: NP69185.RAdVaF7u21CKir Sytv3gdpBXugpdRa0iHwp2oqXkZcA8130 provenance
has publication info: NP69185.RAdVaF7u21CKir Sytv3gdpBXugpdRa0iHwp2oqXkZcA8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69185.RAdVaF7u21CKir Sytv3gdpBXugpdRa0iHwp2oqXkZcA8130 assertion
type: Assertion
description: [This study investigated the contribution of MYOC and OPTN coding variants in Hispanics of Mexican descent with and without POAG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20668460
was generated by: ECO_0000203

NP69186.RAQjwkTBdOPLVk5ILrYj8vb BrGcaa50pZn3Fte7QpTjM
has assertion: NP69186.RAQjwkTBdOPLVk5ILrYj8vb BrGcaa50pZn3Fte7QpTjM130 assertion
has provenance: NP69186.RAQjwkTBdOPLVk5ILrYj8vb BrGcaa50pZn3Fte7QpTjM130 provenance
has publication info: NP69186.RAQjwkTBdOPLVk5ILrYj8vb BrGcaa50pZn3Fte7QpTjM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69186.RAQjwkTBdOPLVk5ILrYj8vb BrGcaa50pZn3Fte7QpTjM130 assertion
type: Assertion
description: [Little evidence for association of the glaucoma gene MYOC with open-angle glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20447966
was generated by: ECO_0000203

NP69189.RATVxcV96vuZ08qoJ6rggFjiyVJ7fkurmBiUn6kv99Pf4
has assertion: NP69189.RATVxcV96vuZ08qoJ6rggFjiyVJ7fkurmBiUn6kv99Pf4130 assertion
has provenance: NP69189.RATVxcV96vuZ08qoJ6rggFjiyVJ7fkurmBiUn6kv99Pf4130 provenance
has publication info: NP69189.RATVxcV96vuZ08qoJ6rggFjiyVJ7fkurmBiUn6kv99Pf4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69189.RATVxcV96vuZ08qoJ6rggFjiyVJ7fkurmBiUn6kv99Pf4130 assertion
type: Assertion
description: [The 2 alleles of the MYOC.mt1 promoter polymorphism were equally distributed among patients with POAG and 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/12215093
was generated by: ECO_0000203

NP69192.RAd58LpQ5Mjq3yNM1ZhZLtwzEe0WzeGALIGvTxaE1DYjU
has assertion: NP69192.RAd58LpQ5Mjq3yNM1ZhZLtwzEe0WzeGALIGvTxaE1DYjU130 assertion
has provenance: NP69192.RAd58LpQ5Mjq3yNM1ZhZLtwzEe0WzeGALIGvTxaE1DYjU130 provenance
has publication info: NP69192.RAd58LpQ5Mjq3yNM1ZhZLtwzEe0WzeGALIGvTxaE1DYjU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69192.RAd58LpQ5Mjq3yNM1ZhZLtwzEe0WzeGALIGvTxaE1DYjU130 assertion
type: Assertion
description: [The association pattern between the genes, MYOC, OPTN, WDR36, and APOE, and POAG in northern Chinese is different from that of southern 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/19145250
was generated by: ECO_0000203

NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq W SSPF5FU
has assertion: NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq W SSPF5FU130 assertion
has provenance: NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq W SSPF5FU130 provenance
has publication info: NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq W SSPF5FU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69194.RATXSXU8AHI1mBapMCgHm57CoeLcHbSeMXq W SSPF5FU130 assertion
type: Assertion
description: [Our methodology allowed to statistically measure the association of a panel of SNPs with a specific 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/18804983
was generated by: ECO_0000203

NP69195.RAcJ3u9dKEGt6z73WgI p51Ld92px bldv cTglzdymls
has assertion: NP69195.RAcJ3u9dKEGt6z73WgI p51Ld92px bldv cTglzdymls130 assertion
has provenance: NP69195.RAcJ3u9dKEGt6z73WgI p51Ld92px bldv cTglzdymls130 provenance
has publication info: NP69195.RAcJ3u9dKEGt6z73WgI p51Ld92px bldv cTglzdymls130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69195.RAcJ3u9dKEGt6z73WgI p51Ld92px bldv cTglzdymls130 assertion
type: Assertion
description: [Our results indicate that Arg206 and Thr381 residues in the motor head region of MYO7A protein are critical sites and the mutations of these residues may lead to the development of nonsyndromic deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19299023
was generated by: ECO_0000203

NP69198.RAbydGSlgF8POUpeVCmuW8wgM5RKNUIrNF1huiFq4NwHQ
has assertion: NP69198.RAbydGSlgF8POUpeVCmuW8wgM5RKNUIrNF1huiFq4NwHQ130 assertion
has provenance: NP69198.RAbydGSlgF8POUpeVCmuW8wgM5RKNUIrNF1huiFq4NwHQ130 provenance
has publication info: NP69198.RAbydGSlgF8POUpeVCmuW8wgM5RKNUIrNF1huiFq4NwHQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69198.RAbydGSlgF8POUpeVCmuW8wgM5RKNUIrNF1huiFq4NwHQ130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP69201.RAblSlS-cGFDAId1XpmcN5A6cJaukOaQk g1Znj-NXMnE
has assertion: NP69201.RAblSlS-cGFDAId1XpmcN5A6cJaukOaQk g1Znj-NXMnE130 assertion
has provenance: NP69201.RAblSlS-cGFDAId1XpmcN5A6cJaukOaQk g1Znj-NXMnE130 provenance
has publication info: NP69201.RAblSlS-cGFDAId1XpmcN5A6cJaukOaQk g1Znj-NXMnE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69201.RAblSlS-cGFDAId1XpmcN5A6cJaukOaQk g1Znj-NXMnE130 assertion
type: Assertion
description: [ABL single nucleotide polymorphisms may masquerade as BCR-ABL mutations associated with resistance to tyrosine kinase inhibitors in patients with chronic 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/18603549
was generated by: ECO_0000203

NP69210.RASxAfGSJ92lMLBpxHiQdplPIP4GTf3hDjfwzDnvCtgl8
has assertion: NP69210.RASxAfGSJ92lMLBpxHiQdplPIP4GTf3hDjfwzDnvCtgl8130 assertion
has provenance: NP69210.RASxAfGSJ92lMLBpxHiQdplPIP4GTf3hDjfwzDnvCtgl8130 provenance
has publication info: NP69210.RASxAfGSJ92lMLBpxHiQdplPIP4GTf3hDjfwzDnvCtgl8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69210.RASxAfGSJ92lMLBpxHiQdplPIP4GTf3hDjfwzDnvCtgl8130 assertion
type: Assertion
description: [Relationship between sex, shape, and substrate in hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18513529
was generated by: ECO_0000203

NP69211.RATjv3uDNtrcjvXxYD2dA3dy2genRC24ZheNUR41pKuPc
has assertion: NP69211.RATjv3uDNtrcjvXxYD2dA3dy2genRC24ZheNUR41pKuPc130 assertion
has provenance: NP69211.RATjv3uDNtrcjvXxYD2dA3dy2genRC24ZheNUR41pKuPc130 provenance
has publication info: NP69211.RATjv3uDNtrcjvXxYD2dA3dy2genRC24ZheNUR41pKuPc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69211.RATjv3uDNtrcjvXxYD2dA3dy2genRC24ZheNUR41pKuPc130 assertion
type: Assertion
description: [This study shows that familial disease is common among infants and children with HCM and that, in most cases, disease is caused by mutations in cardiac sarcomere protein 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/20031618
was generated by: ECO_0000203

NP69214.RAdPGJXj4TR5dCg-YUw-A95mx6awAs8j6sgvqSrPfNByQ
has assertion: NP69214.RAdPGJXj4TR5dCg-YUw-A95mx6awAs8j6sgvqSrPfNByQ130 assertion
has provenance: NP69214.RAdPGJXj4TR5dCg-YUw-A95mx6awAs8j6sgvqSrPfNByQ130 provenance
has publication info: NP69214.RAdPGJXj4TR5dCg-YUw-A95mx6awAs8j6sgvqSrPfNByQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69214.RAdPGJXj4TR5dCg-YUw-A95mx6awAs8j6sgvqSrPfNByQ130 assertion
type: Assertion
description: [The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19293840
was generated by: ECO_0000203

NP69217.RARnImP5Hm6nL vNKbQy9vzb2qPWKBSlb4GYlf-5-Yj88
has assertion: NP69217.RARnImP5Hm6nL vNKbQy9vzb2qPWKBSlb4GYlf-5-Yj88130 assertion
has provenance: NP69217.RARnImP5Hm6nL vNKbQy9vzb2qPWKBSlb4GYlf-5-Yj88130 provenance
has publication info: NP69217.RARnImP5Hm6nL vNKbQy9vzb2qPWKBSlb4GYlf-5-Yj88130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69217.RARnImP5Hm6nL vNKbQy9vzb2qPWKBSlb4GYlf-5-Yj88130 assertion
type: Assertion
description: [Relationship between sex, shape, and substrate in hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18513529
was generated by: ECO_0000203

NP69219.RATjlN3RbyhUilTizhtT1m6hF0ySJXgthi3zhWhtbKo-s
has assertion: NP69219.RATjlN3RbyhUilTizhtT1m6hF0ySJXgthi3zhWhtbKo-s130 assertion
has provenance: NP69219.RATjlN3RbyhUilTizhtT1m6hF0ySJXgthi3zhWhtbKo-s130 provenance
has publication info: NP69219.RATjlN3RbyhUilTizhtT1m6hF0ySJXgthi3zhWhtbKo-s130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69219.RATjlN3RbyhUilTizhtT1m6hF0ySJXgthi3zhWhtbKo-s130 assertion
type: Assertion
description: [The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19293840
was generated by: ECO_0000203

NP69221.RASX01thn7lU18pg7g-j mhnCIXbyQUI9ozi2SHP7PyqA
has assertion: NP69221.RASX01thn7lU18pg7g-j mhnCIXbyQUI9ozi2SHP7PyqA130 assertion
has provenance: NP69221.RASX01thn7lU18pg7g-j mhnCIXbyQUI9ozi2SHP7PyqA130 provenance
has publication info: NP69221.RASX01thn7lU18pg7g-j mhnCIXbyQUI9ozi2SHP7PyqA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69221.RASX01thn7lU18pg7g-j mhnCIXbyQUI9ozi2SHP7PyqA130 assertion
type: Assertion
description: [Failure to find an association between myosin heavy chain 9, non-muscle (MYH9) and schizophrenia: a three-stage case-control 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/20188514
was generated by: ECO_0000203

NP69222.RAb9nGElGwUXesZ6QzdLUIZcMM1yIii9xU6U90xr1UTtQ
has assertion: NP69222.RAb9nGElGwUXesZ6QzdLUIZcMM1yIii9xU6U90xr1UTtQ130 assertion
has provenance: NP69222.RAb9nGElGwUXesZ6QzdLUIZcMM1yIii9xU6U90xr1UTtQ130 provenance
has publication info: NP69222.RAb9nGElGwUXesZ6QzdLUIZcMM1yIii9xU6U90xr1UTtQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69222.RAb9nGElGwUXesZ6QzdLUIZcMM1yIii9xU6U90xr1UTtQ130 assertion
type: Assertion
description: [We searched for mutations in MYH9 exons 1, 16, 26, and 30 in a total of 157 Japanese patients with nonsyndromic deafness without known cause of hearing loss, but no mutations were 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/19645626
was generated by: ECO_0000203

NP69223.RAZzDTIJTy2m8WmIGSxqP8Vn8M2tREgrCqz3CBi yPLpg
has assertion: NP69223.RAZzDTIJTy2m8WmIGSxqP8Vn8M2tREgrCqz3CBi yPLpg130 assertion
has provenance: NP69223.RAZzDTIJTy2m8WmIGSxqP8Vn8M2tREgrCqz3CBi yPLpg130 provenance
has publication info: NP69223.RAZzDTIJTy2m8WmIGSxqP8Vn8M2tREgrCqz3CBi yPLpg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69223.RAZzDTIJTy2m8WmIGSxqP8Vn8M2tREgrCqz3CBi yPLpg130 assertion
type: Assertion
description: [Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19412328
was generated by: ECO_0000203

NP69228.RAVtcAMn8n8LhZsIkSyDMS5mfsoeWWRgs PT5c8NxHwNw
has assertion: NP69228.RAVtcAMn8n8LhZsIkSyDMS5mfsoeWWRgs PT5c8NxHwNw130 assertion
has provenance: NP69228.RAVtcAMn8n8LhZsIkSyDMS5mfsoeWWRgs PT5c8NxHwNw130 provenance
has publication info: NP69228.RAVtcAMn8n8LhZsIkSyDMS5mfsoeWWRgs PT5c8NxHwNw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69228.RAVtcAMn8n8LhZsIkSyDMS5mfsoeWWRgs PT5c8NxHwNw130 assertion
type: Assertion
description: [Little evidence for a role of somatic MYH11 mutations in the formation of breast or prostate cancers was obtained in 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/18796164
was generated by: ECO_0000203

NP69229.RAUgygJLDpGh-87UbLKgujeH5muNGHWJwALBqDyLg NiI
has assertion: NP69229.RAUgygJLDpGh-87UbLKgujeH5muNGHWJwALBqDyLg NiI130 assertion
has provenance: NP69229.RAUgygJLDpGh-87UbLKgujeH5muNGHWJwALBqDyLg NiI130 provenance
has publication info: NP69229.RAUgygJLDpGh-87UbLKgujeH5muNGHWJwALBqDyLg NiI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69229.RAUgygJLDpGh-87UbLKgujeH5muNGHWJwALBqDyLg NiI130 assertion
type: Assertion
description: [Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19536092
was generated by: ECO_0000203

NP69232.RAXr2lMjia2BcM8KwmekFW-HCpSrN2V8WdUUj emLVRqU
has assertion: NP69232.RAXr2lMjia2BcM8KwmekFW-HCpSrN2V8WdUUj emLVRqU130 assertion
has provenance: NP69232.RAXr2lMjia2BcM8KwmekFW-HCpSrN2V8WdUUj emLVRqU130 provenance
has publication info: NP69232.RAXr2lMjia2BcM8KwmekFW-HCpSrN2V8WdUUj emLVRqU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69232.RAXr2lMjia2BcM8KwmekFW-HCpSrN2V8WdUUj emLVRqU130 assertion
type: Assertion
description: [These results demonstrate a clear association between polymorphisms in the IRAK4 gene and serum IgE levels in patients with CRS 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/19254290
was generated by: ECO_0000203

NP69241.RAYOw6cr9gzaKisR3JRVm72279XintEXfowvda2r5-jKo
has assertion: NP69241.RAYOw6cr9gzaKisR3JRVm72279XintEXfowvda2r5-jKo130 assertion
has provenance: NP69241.RAYOw6cr9gzaKisR3JRVm72279XintEXfowvda2r5-jKo130 provenance
has publication info: NP69241.RAYOw6cr9gzaKisR3JRVm72279XintEXfowvda2r5-jKo130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69241.RAYOw6cr9gzaKisR3JRVm72279XintEXfowvda2r5-jKo130 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

NP69244.RAcFY3tza52jcBwjoQpbRKxa38eACYlT2ZpZhsS-HoKVM
has assertion: NP69244.RAcFY3tza52jcBwjoQpbRKxa38eACYlT2ZpZhsS-HoKVM130 assertion
has provenance: NP69244.RAcFY3tza52jcBwjoQpbRKxa38eACYlT2ZpZhsS-HoKVM130 provenance
has publication info: NP69244.RAcFY3tza52jcBwjoQpbRKxa38eACYlT2ZpZhsS-HoKVM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69244.RAcFY3tza52jcBwjoQpbRKxa38eACYlT2ZpZhsS-HoKVM130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP69246.RAVyTgGhGtTtONpzAyrpQ3nq52l7BoF-utmfk4OWKHnnM
has assertion: NP69246.RAVyTgGhGtTtONpzAyrpQ3nq52l7BoF-utmfk4OWKHnnM130 assertion
has provenance: NP69246.RAVyTgGhGtTtONpzAyrpQ3nq52l7BoF-utmfk4OWKHnnM130 provenance
has publication info: NP69246.RAVyTgGhGtTtONpzAyrpQ3nq52l7BoF-utmfk4OWKHnnM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69246.RAVyTgGhGtTtONpzAyrpQ3nq52l7BoF-utmfk4OWKHnnM130 assertion
type: Assertion
description: [Relationship between sex, shape, and substrate in hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18513529
was generated by: ECO_0000203

NP69247.RAcDybtpHVfZcwMs4yGsaKZSaITFr8fpVLkgXxCJ2jjyk
has assertion: NP69247.RAcDybtpHVfZcwMs4yGsaKZSaITFr8fpVLkgXxCJ2jjyk130 assertion
has provenance: NP69247.RAcDybtpHVfZcwMs4yGsaKZSaITFr8fpVLkgXxCJ2jjyk130 provenance
has publication info: NP69247.RAcDybtpHVfZcwMs4yGsaKZSaITFr8fpVLkgXxCJ2jjyk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69247.RAcDybtpHVfZcwMs4yGsaKZSaITFr8fpVLkgXxCJ2jjyk130 assertion
type: Assertion
description: [MYH7 mutations, especially in the global region, cause malignant clinical 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/18383048
was generated by: ECO_0000203

NP69248.RAXdVz9U-U-di89O-ukYeBTGb2dtI82obQRIvjiAMMbJQ
has assertion: NP69248.RAXdVz9U-U-di89O-ukYeBTGb2dtI82obQRIvjiAMMbJQ130 assertion
has provenance: NP69248.RAXdVz9U-U-di89O-ukYeBTGb2dtI82obQRIvjiAMMbJQ130 provenance
has publication info: NP69248.RAXdVz9U-U-di89O-ukYeBTGb2dtI82obQRIvjiAMMbJQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69248.RAXdVz9U-U-di89O-ukYeBTGb2dtI82obQRIvjiAMMbJQ130 assertion
type: Assertion
description: [The conclusion is the missense MYBPC3 mutation E334K destabilizes its protein through UPS and may contribute to cardiac dysfunction in HCM through impairment of the ubiquitin-proteasome 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/18929575
was generated by: ECO_0000203

NP69252.RAYJrIMxpkVW6VL2gsVBg 0kK6 X e23PceS2WxaSEPVA
has assertion: NP69252.RAYJrIMxpkVW6VL2gsVBg 0kK6 X e23PceS2WxaSEPVA130 assertion
has provenance: NP69252.RAYJrIMxpkVW6VL2gsVBg 0kK6 X e23PceS2WxaSEPVA130 provenance
has publication info: NP69252.RAYJrIMxpkVW6VL2gsVBg 0kK6 X e23PceS2WxaSEPVA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69252.RAYJrIMxpkVW6VL2gsVBg 0kK6 X e23PceS2WxaSEPVA130 assertion
type: Assertion
description: [Overall, 25 of 47 (53%) patients had myofilament-HCM, including 12 with MYBPC3-HCM and 9 with MYH7-HCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19808356
was generated by: ECO_0000203

NP69253.RAdmaMYc5X3p7vgYNezBpfKdudAGG37gKlHNtTNWzP3mU
has assertion: NP69253.RAdmaMYc5X3p7vgYNezBpfKdudAGG37gKlHNtTNWzP3mU130 assertion
has provenance: NP69253.RAdmaMYc5X3p7vgYNezBpfKdudAGG37gKlHNtTNWzP3mU130 provenance
has publication info: NP69253.RAdmaMYc5X3p7vgYNezBpfKdudAGG37gKlHNtTNWzP3mU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69253.RAdmaMYc5X3p7vgYNezBpfKdudAGG37gKlHNtTNWzP3mU130 assertion
type: Assertion
description: [This study shows that familial disease is common among infants and children with HCM and that, in most cases, disease is caused by mutations in cardiac sarcomere protein 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/20031618
was generated by: ECO_0000203

NP69254.RAQvKKAEZKdTdRRvJ9F08e6TNj-yFEo0ahQphEPDwvSuk
has assertion: NP69254.RAQvKKAEZKdTdRRvJ9F08e6TNj-yFEo0ahQphEPDwvSuk130 assertion
has provenance: NP69254.RAQvKKAEZKdTdRRvJ9F08e6TNj-yFEo0ahQphEPDwvSuk130 provenance
has publication info: NP69254.RAQvKKAEZKdTdRRvJ9F08e6TNj-yFEo0ahQphEPDwvSuk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69254.RAQvKKAEZKdTdRRvJ9F08e6TNj-yFEo0ahQphEPDwvSuk130 assertion
type: Assertion
description: [MYBPC3 mutation is presented in a small portion of Han Chinese patients with HCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20021930
was generated by: ECO_0000203

NP69262.RARiD6dha9 BKAVOH3aEqdsWpuKZSa0OBxBaWzg4TQbPw
has assertion: NP69262.RARiD6dha9 BKAVOH3aEqdsWpuKZSa0OBxBaWzg4TQbPw130 assertion
has provenance: NP69262.RARiD6dha9 BKAVOH3aEqdsWpuKZSa0OBxBaWzg4TQbPw130 provenance
has publication info: NP69262.RARiD6dha9 BKAVOH3aEqdsWpuKZSa0OBxBaWzg4TQbPw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69262.RARiD6dha9 BKAVOH3aEqdsWpuKZSa0OBxBaWzg4TQbPw130 assertion
type: Assertion
description: [Multiple loci influence erythrocyte phenotypes in the CHARGE 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/19862010
was generated by: ECO_0000203

NP69265.RASv7Ivkyy jRXnI 7gkMXYshj2dkid7pl6rEBXRp4irY
has assertion: NP69265.RASv7Ivkyy jRXnI 7gkMXYshj2dkid7pl6rEBXRp4irY130 assertion
has provenance: NP69265.RASv7Ivkyy jRXnI 7gkMXYshj2dkid7pl6rEBXRp4irY130 provenance
has publication info: NP69265.RASv7Ivkyy jRXnI 7gkMXYshj2dkid7pl6rEBXRp4irY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69265.RASv7Ivkyy jRXnI 7gkMXYshj2dkid7pl6rEBXRp4irY130 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

NP69268.RAf5Lfec-u336cLWIJiGGUTlnto-yxsOUSoIHb1dXPUsQ
has assertion: NP69268.RAf5Lfec-u336cLWIJiGGUTlnto-yxsOUSoIHb1dXPUsQ130 assertion
has provenance: NP69268.RAf5Lfec-u336cLWIJiGGUTlnto-yxsOUSoIHb1dXPUsQ130 provenance
has publication info: NP69268.RAf5Lfec-u336cLWIJiGGUTlnto-yxsOUSoIHb1dXPUsQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69268.RAf5Lfec-u336cLWIJiGGUTlnto-yxsOUSoIHb1dXPUsQ130 assertion
type: Assertion
description: [Carriers of the MYH Y165C or G382D mutant alleles do not appear to be at increased risk 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/18454351
was generated by: ECO_0000203

NP69269.RAesZ9ajWo6efpj71RFRBxzBE1S4eYc1qv9-JIhmz6X6E
has assertion: NP69269.RAesZ9ajWo6efpj71RFRBxzBE1S4eYc1qv9-JIhmz6X6E130 assertion
has provenance: NP69269.RAesZ9ajWo6efpj71RFRBxzBE1S4eYc1qv9-JIhmz6X6E130 provenance
has publication info: NP69269.RAesZ9ajWo6efpj71RFRBxzBE1S4eYc1qv9-JIhmz6X6E130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69269.RAesZ9ajWo6efpj71RFRBxzBE1S4eYc1qv9-JIhmz6X6E130 assertion
type: Assertion
description: [Novel variants at KCTD10, MVK, and MMAB genes interact with dietary carbohydrates to modulate HDL-cholesterol concentrations in the Genetics of Lipid Lowering Drugs and Diet Network 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/19605566
was generated by: ECO_0000203

NP69270.RAbK5ObY701OtEkbFKOEAxWtb7NeWB21ui7EtQSFq6B0k
has assertion: NP69270.RAbK5ObY701OtEkbFKOEAxWtb7NeWB21ui7EtQSFq6B0k130 assertion
has provenance: NP69270.RAbK5ObY701OtEkbFKOEAxWtb7NeWB21ui7EtQSFq6B0k130 provenance
has publication info: NP69270.RAbK5ObY701OtEkbFKOEAxWtb7NeWB21ui7EtQSFq6B0k130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69270.RAbK5ObY701OtEkbFKOEAxWtb7NeWB21ui7EtQSFq6B0k130 assertion
type: Assertion
description: [MUTYH Gln324His gene polymorphism and genetic susceptibility for lung cancer 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/19161591
was generated by: ECO_0000203

NP69274.RAfW EqDmPulQPKLV4FxFWv7nbJYPrZ1p75OM7lGadFLA
has assertion: NP69274.RAfW EqDmPulQPKLV4FxFWv7nbJYPrZ1p75OM7lGadFLA130 assertion
has provenance: NP69274.RAfW EqDmPulQPKLV4FxFWv7nbJYPrZ1p75OM7lGadFLA130 provenance
has publication info: NP69274.RAfW EqDmPulQPKLV4FxFWv7nbJYPrZ1p75OM7lGadFLA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69274.RAfW EqDmPulQPKLV4FxFWv7nbJYPrZ1p75OM7lGadFLA130 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

NP69288.RAS4aLH3hO4PD-r77or9- B-h-1n10t6ofD7mfNDKpGN8
has assertion: NP69288.RAS4aLH3hO4PD-r77or9- B-h-1n10t6ofD7mfNDKpGN8130 assertion
has provenance: NP69288.RAS4aLH3hO4PD-r77or9- B-h-1n10t6ofD7mfNDKpGN8130 provenance
has publication info: NP69288.RAS4aLH3hO4PD-r77or9- B-h-1n10t6ofD7mfNDKpGN8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69288.RAS4aLH3hO4PD-r77or9- B-h-1n10t6ofD7mfNDKpGN8130 assertion
type: Assertion
description: [Independent pharmacogenomic determinants associated with treatment outcome were identified in subsets of Taiwanese 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/19774638
was generated by: ECO_0000203

NP69289.RAfHa2DtnXv3yFx37WZ4lQ1dS36yxpRNPJZldeM7ji76A
has assertion: NP69289.RAfHa2DtnXv3yFx37WZ4lQ1dS36yxpRNPJZldeM7ji76A130 assertion
has provenance: NP69289.RAfHa2DtnXv3yFx37WZ4lQ1dS36yxpRNPJZldeM7ji76A130 provenance
has publication info: NP69289.RAfHa2DtnXv3yFx37WZ4lQ1dS36yxpRNPJZldeM7ji76A130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69289.RAfHa2DtnXv3yFx37WZ4lQ1dS36yxpRNPJZldeM7ji76A130 assertion
type: Assertion
description: [Candidate gene association studies and risk of childhood acute lymphoblastic leukemia: a systematic review 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/20511665
was generated by: ECO_0000203

NP69293.RAaBmN-eBNyxeRf5B9Xh UA2SWQ1TioQ4rFnK-IMUhlbM
has assertion: NP69293.RAaBmN-eBNyxeRf5B9Xh UA2SWQ1TioQ4rFnK-IMUhlbM130 assertion
has provenance: NP69293.RAaBmN-eBNyxeRf5B9Xh UA2SWQ1TioQ4rFnK-IMUhlbM130 provenance
has publication info: NP69293.RAaBmN-eBNyxeRf5B9Xh UA2SWQ1TioQ4rFnK-IMUhlbM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69293.RAaBmN-eBNyxeRf5B9Xh UA2SWQ1TioQ4rFnK-IMUhlbM130 assertion
type: Assertion
description: [Association between polymorphisms of folate-metabolizing enzymes and hematological 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/18774170
was generated by: ECO_0000203

NP69297.RAZ2y3qXyq-ztSVUYTw6aYflIQyYpbwqxPWAwclZfwIa0
has assertion: NP69297.RAZ2y3qXyq-ztSVUYTw6aYflIQyYpbwqxPWAwclZfwIa0130 assertion
has provenance: NP69297.RAZ2y3qXyq-ztSVUYTw6aYflIQyYpbwqxPWAwclZfwIa0130 provenance
has publication info: NP69297.RAZ2y3qXyq-ztSVUYTw6aYflIQyYpbwqxPWAwclZfwIa0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69297.RAZ2y3qXyq-ztSVUYTw6aYflIQyYpbwqxPWAwclZfwIa0130 assertion
type: Assertion
description: [Polymorphisms in mitochondrial genes 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/19064571
was generated by: ECO_0000203

NP69302.RAQIxx-rfSirBoIrrxt85ap8swBgJnxcsA5CcsQcmh128
has assertion: NP69302.RAQIxx-rfSirBoIrrxt85ap8swBgJnxcsA5CcsQcmh128130 assertion
has provenance: NP69302.RAQIxx-rfSirBoIrrxt85ap8swBgJnxcsA5CcsQcmh128130 provenance
has publication info: NP69302.RAQIxx-rfSirBoIrrxt85ap8swBgJnxcsA5CcsQcmh128130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69302.RAQIxx-rfSirBoIrrxt85ap8swBgJnxcsA5CcsQcmh128130 assertion
type: Assertion
description: [Our study indicates interesting new candidate genes and functional pathways for further study and confirms earlier 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/19161160
was generated by: ECO_0000203

NP69303.RASnZsnhJCEdp3Ex8m6oeUV8aJ2Sp5Z-ckpSXZaecpl6o
has assertion: NP69303.RASnZsnhJCEdp3Ex8m6oeUV8aJ2Sp5Z-ckpSXZaecpl6o130 assertion
has provenance: NP69303.RASnZsnhJCEdp3Ex8m6oeUV8aJ2Sp5Z-ckpSXZaecpl6o130 provenance
has publication info: NP69303.RASnZsnhJCEdp3Ex8m6oeUV8aJ2Sp5Z-ckpSXZaecpl6o130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69303.RASnZsnhJCEdp3Ex8m6oeUV8aJ2Sp5Z-ckpSXZaecpl6o130 assertion
type: Assertion
description: [Polymorphisms in the folate/Hcy pathway are associated with tHcy and folate derivative levels. In African American and Caucasian women, different factors are associated with folate/Hcy phenotypes and may contribute to race-specific differences in the risks of a range of pregnancy-related pathologies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20544798
was generated by: ECO_0000203

NP69305.RAe2MDWo-3fmw1FGYz0FzIsihjbkfKUUur2Sdc1WTZYJE
has assertion: NP69305.RAe2MDWo-3fmw1FGYz0FzIsihjbkfKUUur2Sdc1WTZYJE130 assertion
has provenance: NP69305.RAe2MDWo-3fmw1FGYz0FzIsihjbkfKUUur2Sdc1WTZYJE130 provenance
has publication info: NP69305.RAe2MDWo-3fmw1FGYz0FzIsihjbkfKUUur2Sdc1WTZYJE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69305.RAe2MDWo-3fmw1FGYz0FzIsihjbkfKUUur2Sdc1WTZYJE130 assertion
type: Assertion
description: [In this study, we determined total plasma homocysteine levels and MTRR A66G polymorphism in 114 patients with vascular disease: 58 patients with deep-vein thrombosis, 56 patients with arterial thrombosis, and 95 healthy subjects from the Sicilian 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/19348062
was generated by: ECO_0000203

NP69306.RAR65eNTvvnyerPOmIZ6 HRh0jVeokmq6ddQ4DkGNTVkw
has assertion: NP69306.RAR65eNTvvnyerPOmIZ6 HRh0jVeokmq6ddQ4DkGNTVkw130 assertion
has provenance: NP69306.RAR65eNTvvnyerPOmIZ6 HRh0jVeokmq6ddQ4DkGNTVkw130 provenance
has publication info: NP69306.RAR65eNTvvnyerPOmIZ6 HRh0jVeokmq6ddQ4DkGNTVkw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69306.RAR65eNTvvnyerPOmIZ6 HRh0jVeokmq6ddQ4DkGNTVkw130 assertion
type: Assertion
description: [Hyperhomocysteinemia, C677T MTHFR and C1561T GCPII are risk factors for 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/19394322
was generated by: ECO_0000203

NP69310.RAX31koikYx3OlsnGiw571uZ1zv3GCeDEeW79Hd FkNLA
has assertion: NP69310.RAX31koikYx3OlsnGiw571uZ1zv3GCeDEeW79Hd FkNLA130 assertion
has provenance: NP69310.RAX31koikYx3OlsnGiw571uZ1zv3GCeDEeW79Hd FkNLA130 provenance
has publication info: NP69310.RAX31koikYx3OlsnGiw571uZ1zv3GCeDEeW79Hd FkNLA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69310.RAX31koikYx3OlsnGiw571uZ1zv3GCeDEeW79Hd FkNLA130 assertion
type: Assertion
description: [The frequencies of MTRR 66A allele (12.7 vs. 21.0%) and SHMT 1420T allele (27.9 vs. 45.3%) were lower in autistic group compared with nonautistic group with odds ratios 0.55 (95% CI: 0.35-0.86) and 0.44 (95% CI: 0.31-0.62), respectively, indicating reduced 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/19440165
was generated by: ECO_0000203

NP69315.RATC8e0GF7quMUcvnX4tsnXZ1ZTj3hGUMFFs-9LVPm7NM
has assertion: NP69315.RATC8e0GF7quMUcvnX4tsnXZ1ZTj3hGUMFFs-9LVPm7NM130 assertion
has provenance: NP69315.RATC8e0GF7quMUcvnX4tsnXZ1ZTj3hGUMFFs-9LVPm7NM130 provenance
has publication info: NP69315.RATC8e0GF7quMUcvnX4tsnXZ1ZTj3hGUMFFs-9LVPm7NM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69315.RATC8e0GF7quMUcvnX4tsnXZ1ZTj3hGUMFFs-9LVPm7NM130 assertion
type: Assertion
description: [High-throughput multiplex single-nucleotide polymorphism (SNP) analysis in genes involved in methionine 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/18427977
was generated by: ECO_0000203

NP69326.RAYyFZ88LSSgeD3CyzONqGokJCiVTUfz5UpctPYNKxL80
has assertion: NP69326.RAYyFZ88LSSgeD3CyzONqGokJCiVTUfz5UpctPYNKxL80130 assertion
has provenance: NP69326.RAYyFZ88LSSgeD3CyzONqGokJCiVTUfz5UpctPYNKxL80130 provenance
has publication info: NP69326.RAYyFZ88LSSgeD3CyzONqGokJCiVTUfz5UpctPYNKxL80130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69326.RAYyFZ88LSSgeD3CyzONqGokJCiVTUfz5UpctPYNKxL80130 assertion
type: Assertion
description: [Alcohol drinking and one-carbon metabolism-related gene polymorphisms on pancreatic 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/18843018
was generated by: ECO_0000203

NP69340.RAblkOanm6ZZPq2oD0WlY obQfRqk 5QpYJ v YKiHo6Y
has assertion: NP69340.RAblkOanm6ZZPq2oD0WlY obQfRqk 5QpYJ v YKiHo6Y130 assertion
has provenance: NP69340.RAblkOanm6ZZPq2oD0WlY obQfRqk 5QpYJ v YKiHo6Y130 provenance
has publication info: NP69340.RAblkOanm6ZZPq2oD0WlY obQfRqk 5QpYJ v YKiHo6Y130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69340.RAblkOanm6ZZPq2oD0WlY obQfRqk 5QpYJ v YKiHo6Y130 assertion
type: Assertion
description: [PTEN identified as important risk factor of chronic obstructive pulmonary 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/19625176
was generated by: ECO_0000203

NP69341.RARQVz-SwefCAftwhyXLjhNJhX 3wu2eSdT3TX4lY-Faw
has assertion: NP69341.RARQVz-SwefCAftwhyXLjhNJhX 3wu2eSdT3TX4lY-Faw130 assertion
has provenance: NP69341.RARQVz-SwefCAftwhyXLjhNJhX 3wu2eSdT3TX4lY-Faw130 provenance
has publication info: NP69341.RARQVz-SwefCAftwhyXLjhNJhX 3wu2eSdT3TX4lY-Faw130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69341.RARQVz-SwefCAftwhyXLjhNJhX 3wu2eSdT3TX4lY-Faw130 assertion
type: Assertion
description: [The relationship between homocysteine and genes of folate-related enzymes in migraine 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/19619240
was generated by: ECO_0000203

NP69342.RAchyMB2HoyD68RjqTsD0FvKOS2o8hxlSAdD8txs5XdTI
has assertion: NP69342.RAchyMB2HoyD68RjqTsD0FvKOS2o8hxlSAdD8txs5XdTI130 assertion
has provenance: NP69342.RAchyMB2HoyD68RjqTsD0FvKOS2o8hxlSAdD8txs5XdTI130 provenance
has publication info: NP69342.RAchyMB2HoyD68RjqTsD0FvKOS2o8hxlSAdD8txs5XdTI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69342.RAchyMB2HoyD68RjqTsD0FvKOS2o8hxlSAdD8txs5XdTI130 assertion
type: Assertion
description: [Association of folate-pathway gene polymorphisms with the risk of prostate cancer: a population-based nested case-control study, systematic review, 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/19706844
was generated by: ECO_0000203

NP69343.RAeULz1nzUTkLAzJooX6zDRrxLWuwLNTbzWlaIetC8iNA
has assertion: NP69343.RAeULz1nzUTkLAzJooX6zDRrxLWuwLNTbzWlaIetC8iNA130 assertion
has provenance: NP69343.RAeULz1nzUTkLAzJooX6zDRrxLWuwLNTbzWlaIetC8iNA130 provenance
has publication info: NP69343.RAeULz1nzUTkLAzJooX6zDRrxLWuwLNTbzWlaIetC8iNA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69343.RAeULz1nzUTkLAzJooX6zDRrxLWuwLNTbzWlaIetC8iNA130 assertion
type: Assertion
description: [Long-term follow-up is needed to test associations with metastases and mortality, and the observed genetic effects require replication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20852008
was generated by: ECO_0000203

NP69344.RATj33pugBPBCtVs1gZxqizRzHvH6h0P5qLfzqIRgkMl4
has assertion: NP69344.RATj33pugBPBCtVs1gZxqizRzHvH6h0P5qLfzqIRgkMl4130 assertion
has provenance: NP69344.RATj33pugBPBCtVs1gZxqizRzHvH6h0P5qLfzqIRgkMl4130 provenance
has publication info: NP69344.RATj33pugBPBCtVs1gZxqizRzHvH6h0P5qLfzqIRgkMl4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69344.RATj33pugBPBCtVs1gZxqizRzHvH6h0P5qLfzqIRgkMl4130 assertion
type: Assertion
description: [the polymorphism MTHFR C677T is clearly related to prostatic carcinogenesis, on the contrary to the other polymorphisms studied, although the MTR 2756 allele C acts as a factor of tumor aggressiveness, this being found in tumors with high carcinogenic potential.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17967524
was generated by: ECO_0000203

NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z 30Ovk
has assertion: NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z 30Ovk130 assertion
has provenance: NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z 30Ovk130 provenance
has publication info: NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z 30Ovk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z 30Ovk130 assertion
type: Assertion
description: [Twenty-three polymorphisms in 22 potential PAD candidate genes (F2, FGB, MTHFR, ITGB3, ACE, AGT, IL6, CCL2, ICAM1, SELE, MMP9, PPARG, MMP1, ADD1, P2RY12, LIPC, PLA2G7, SCARB1, MMP3, MTTP, LPA, CHRNA3) showed a significant association in individual 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/19435865
was generated by: ECO_0000203

NP69351.RAdl-n-ji6Hvqj1OQmD5aUl3s93H Oor0opmrqNhXSAYA
has assertion: NP69351.RAdl-n-ji6Hvqj1OQmD5aUl3s93H Oor0opmrqNhXSAYA130 assertion
has provenance: NP69351.RAdl-n-ji6Hvqj1OQmD5aUl3s93H Oor0opmrqNhXSAYA130 provenance
has publication info: NP69351.RAdl-n-ji6Hvqj1OQmD5aUl3s93H Oor0opmrqNhXSAYA130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69351.RAdl-n-ji6Hvqj1OQmD5aUl3s93H Oor0opmrqNhXSAYA130 assertion
type: Assertion
description: [Combined effects of single-nucleotide polymorphisms in GCK, GCKR, G6PC2 and MTNR1B on fasting plasma glucose and type 2 diabetes 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/19533084
was generated by: ECO_0000203

NP69352.RAWh5Lmr650ltJHh6CQegBqBpmZocRuLiEZhq29-L6pR8
has assertion: NP69352.RAWh5Lmr650ltJHh6CQegBqBpmZocRuLiEZhq29-L6pR8130 assertion
has provenance: NP69352.RAWh5Lmr650ltJHh6CQegBqBpmZocRuLiEZhq29-L6pR8130 provenance
has publication info: NP69352.RAWh5Lmr650ltJHh6CQegBqBpmZocRuLiEZhq29-L6pR8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69352.RAWh5Lmr650ltJHh6CQegBqBpmZocRuLiEZhq29-L6pR8130 assertion
type: Assertion
description: [Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A, and MTNR1B affect different aspects of pancreatic beta-cell function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19833888
was generated by: ECO_0000203

NP69354.RATTjlOQeuHktbJsWDOBkZpWuxY-Clte-hqtaE1dOEWIc
has assertion: NP69354.RATTjlOQeuHktbJsWDOBkZpWuxY-Clte-hqtaE1dOEWIc130 assertion
has provenance: NP69354.RATTjlOQeuHktbJsWDOBkZpWuxY-Clte-hqtaE1dOEWIc130 provenance
has publication info: NP69354.RATTjlOQeuHktbJsWDOBkZpWuxY-Clte-hqtaE1dOEWIc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69354.RATTjlOQeuHktbJsWDOBkZpWuxY-Clte-hqtaE1dOEWIc130 assertion
type: Assertion
description: [Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19060908
was generated by: ECO_0000203

NP69355.RAcuo0OM0d2GIktwWL6Z42akE072Ts6vvRTVGVt6BJo6Q
has assertion: NP69355.RAcuo0OM0d2GIktwWL6Z42akE072Ts6vvRTVGVt6BJo6Q130 assertion
has provenance: NP69355.RAcuo0OM0d2GIktwWL6Z42akE072Ts6vvRTVGVt6BJo6Q130 provenance
has publication info: NP69355.RAcuo0OM0d2GIktwWL6Z42akE072Ts6vvRTVGVt6BJo6Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP69355.RAcuo0OM0d2GIktwWL6Z42akE072Ts6vvRTVGVt6BJo6Q130 assertion
type: Assertion
description: [A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes 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/19060909
was generated by: ECO_0000203

NP69364.RATmGVSr3PJJvU9MQVtjDy4Adr9ZIT9y5SDBw1oKntlHQ
has assertion: NP69364.RATmGVSr3PJJvU9MQVtjDy4Adr9ZIT9y5SDBw1oKntlHQ130 assertion
has provenance: NP69364.RATmGVSr3PJJvU9MQVtjDy4Adr9ZIT9y5SDBw1oKntlHQ130 provenance
has publication info: NP69364.RATmGVSr3PJJvU9MQVtjDy4Adr9ZIT9y5SDBw1oKntlHQ130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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

NP69364.RATmGVSr3PJJvU9MQVtjDy4Adr9ZIT9y5SDBw1oKntlHQ130 assertion
type: Assertion
description: [Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19710684
was generated by: ECO_0000203

NP69367.RAc92NVcd38lUpuO72CvBRgP2Yio A3nyrOnLSAKiFZjM
has assertion: NP69367.RAc92NVcd38lUpuO72CvBRgP2Yio A3nyrOnLSAKiFZjM130 assertion
has provenance: NP69367.RAc92NVcd38lUpuO72CvBRgP2Yio A3nyrOnLSAKiFZjM130 provenance
has publication info: NP69367.RAc92NVcd38lUpuO72CvBRgP2Yio A3nyrOnLSAKiFZjM130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69367.RAc92NVcd38lUpuO72CvBRgP2Yio A3nyrOnLSAKiFZjM130 assertion
type: Assertion
description: [Contrary to numerous suggestions in various publications, we did not confirm the correlation between MTHFR 677C>T polymorphism and the influence on the risk of ovarian cancer in BRCA1 mutation carriers in the investigated group of Polish 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/20825051
was generated by: ECO_0000203

NP69373.RAaqwSqv0-6KXf0vgRNJYJ92ey3kr9alELuD7fbG-V8u8
has assertion: NP69373.RAaqwSqv0-6KXf0vgRNJYJ92ey3kr9alELuD7fbG-V8u8130 assertion
has provenance: NP69373.RAaqwSqv0-6KXf0vgRNJYJ92ey3kr9alELuD7fbG-V8u8130 provenance
has publication info: NP69373.RAaqwSqv0-6KXf0vgRNJYJ92ey3kr9alELuD7fbG-V8u8130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69373.RAaqwSqv0-6KXf0vgRNJYJ92ey3kr9alELuD7fbG-V8u8130 assertion
type: Assertion
description: [Association between the methylenetetrahydrofolate reductase polymorphisms and risk of acute lymphoblastic leukemia in Serbian 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/20445408
was generated by: ECO_0000203

NP69377.RAYa36mLe3-Qzv6wXoTruSsW2CoYziAGNvqifY9VL4lfg
has assertion: NP69377.RAYa36mLe3-Qzv6wXoTruSsW2CoYziAGNvqifY9VL4lfg130 assertion
has provenance: NP69377.RAYa36mLe3-Qzv6wXoTruSsW2CoYziAGNvqifY9VL4lfg130 provenance
has publication info: NP69377.RAYa36mLe3-Qzv6wXoTruSsW2CoYziAGNvqifY9VL4lfg130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69377.RAYa36mLe3-Qzv6wXoTruSsW2CoYziAGNvqifY9VL4lfg130 assertion
type: Assertion
description: [Several studies have reported a reduced risk of developing ALL in children with MTHFR 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/18421714
was generated by: ECO_0000203

NP69389.RAXEkmiImJpXKxdQ5NKWp90 1AOjlN8S8baZ5xFoQumBE
has assertion: NP69389.RAXEkmiImJpXKxdQ5NKWp90 1AOjlN8S8baZ5xFoQumBE130 assertion
has provenance: NP69389.RAXEkmiImJpXKxdQ5NKWp90 1AOjlN8S8baZ5xFoQumBE130 provenance
has publication info: NP69389.RAXEkmiImJpXKxdQ5NKWp90 1AOjlN8S8baZ5xFoQumBE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69389.RAXEkmiImJpXKxdQ5NKWp90 1AOjlN8S8baZ5xFoQumBE130 assertion
type: Assertion
description: [The genetics of carotid dissection: meta-analysis of a MTHFR/C677T common molecular 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/18483455
was generated by: ECO_0000203

NP69391.RAe0qrdx7ooT7lNyQ ZXNXk942eV838ObiRqtM0CWi9k4
has assertion: NP69391.RAe0qrdx7ooT7lNyQ ZXNXk942eV838ObiRqtM0CWi9k4130 assertion
has provenance: NP69391.RAe0qrdx7ooT7lNyQ ZXNXk942eV838ObiRqtM0CWi9k4130 provenance
has publication info: NP69391.RAe0qrdx7ooT7lNyQ ZXNXk942eV838ObiRqtM0CWi9k4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69391.RAe0qrdx7ooT7lNyQ ZXNXk942eV838ObiRqtM0CWi9k4130 assertion
type: Assertion
description: [Effect of the methylenetetrahydrofolate reductase gene polymorphisms on homocysteine, folate and vitamin B12 in patients with bipolar disorder and relatives.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18513846
was generated by: ECO_0000203

NP69395.RAX4Bb6eNUTI2kReJ8YgmOJlmI5O2E1xN0z0x9OhlG9vc
has assertion: NP69395.RAX4Bb6eNUTI2kReJ8YgmOJlmI5O2E1xN0z0x9OhlG9vc130 assertion
has provenance: NP69395.RAX4Bb6eNUTI2kReJ8YgmOJlmI5O2E1xN0z0x9OhlG9vc130 provenance
has publication info: NP69395.RAX4Bb6eNUTI2kReJ8YgmOJlmI5O2E1xN0z0x9OhlG9vc130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69395.RAX4Bb6eNUTI2kReJ8YgmOJlmI5O2E1xN0z0x9OhlG9vc130 assertion
type: Assertion
description: [Hereditary thrombophilia promotes induction of nephrosclerosis leading to activation of intraglomerular blood clotting which contributes to CGN 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/19799197
was generated by: ECO_0000203

NP69396.RASKYPrwp tXooR2ojv-tTNI1szaxgFNE0V1bdjG2CtB0
has assertion: NP69396.RASKYPrwp tXooR2ojv-tTNI1szaxgFNE0V1bdjG2CtB0130 assertion
has provenance: NP69396.RASKYPrwp tXooR2ojv-tTNI1szaxgFNE0V1bdjG2CtB0130 provenance
has publication info: NP69396.RASKYPrwp tXooR2ojv-tTNI1szaxgFNE0V1bdjG2CtB0130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69396.RASKYPrwp tXooR2ojv-tTNI1szaxgFNE0V1bdjG2CtB0130 assertion
type: Assertion
description: [Rapid multiplexed genotyping for hereditary thrombophilia by SELDI-TOF mass spectrometry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20186013
was generated by: ECO_0000203

NP69399.RAS4l4EYJoT6trm8z6WJG40YLfPU-MP-rR4ufA9OtqoD4
has assertion: NP69399.RAS4l4EYJoT6trm8z6WJG40YLfPU-MP-rR4ufA9OtqoD4130 assertion
has provenance: NP69399.RAS4l4EYJoT6trm8z6WJG40YLfPU-MP-rR4ufA9OtqoD4130 provenance
has publication info: NP69399.RAS4l4EYJoT6trm8z6WJG40YLfPU-MP-rR4ufA9OtqoD4130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69399.RAS4l4EYJoT6trm8z6WJG40YLfPU-MP-rR4ufA9OtqoD4130 assertion
type: Assertion
description: [the Pronto ThromboRisk kit allows fast, precise, and reliable testing for the three genetic 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/15356875
was generated by: ECO_0000203

NP69401.RAfKD9Qclgw0me5B4xaApw-y1ipr1Zfq1qrD2ZWW2t4QY
has assertion: NP69401.RAfKD9Qclgw0me5B4xaApw-y1ipr1Zfq1qrD2ZWW2t4QY130 assertion
has provenance: NP69401.RAfKD9Qclgw0me5B4xaApw-y1ipr1Zfq1qrD2ZWW2t4QY130 provenance
has publication info: NP69401.RAfKD9Qclgw0me5B4xaApw-y1ipr1Zfq1qrD2ZWW2t4QY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69401.RAfKD9Qclgw0me5B4xaApw-y1ipr1Zfq1qrD2ZWW2t4QY130 assertion
type: Assertion
description: [Thrombophilia is associated with increased risks of VTE in women taking oral oestrogen preparations and patients undergoing major elective orthopaedic surgery, and of VTE and adverse pregnancy outcomes in women with thrombophilia during pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16595080
was generated by: ECO_0000203

NP69412.RAZWXtuOJ-k4AWz37enYk8OMMpBNUlvjD1g0wr-am6NlY
has assertion: NP69412.RAZWXtuOJ-k4AWz37enYk8OMMpBNUlvjD1g0wr-am6NlY130 assertion
has provenance: NP69412.RAZWXtuOJ-k4AWz37enYk8OMMpBNUlvjD1g0wr-am6NlY130 provenance
has publication info: NP69412.RAZWXtuOJ-k4AWz37enYk8OMMpBNUlvjD1g0wr-am6NlY130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69412.RAZWXtuOJ-k4AWz37enYk8OMMpBNUlvjD1g0wr-am6NlY130 assertion
type: Assertion
description: [Methylenetetrahydrofolate reductase gene polymorphisms: genomic predictors of clinical response to fluoropyrimidine-based chemotherapy 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/18612168
was generated by: ECO_0000203

NP69413.RAWilyFuCyPSndzh4jpQXIa7kS0N9P8UgKADFMwXg6mrk
has assertion: NP69413.RAWilyFuCyPSndzh4jpQXIa7kS0N9P8UgKADFMwXg6mrk130 assertion
has provenance: NP69413.RAWilyFuCyPSndzh4jpQXIa7kS0N9P8UgKADFMwXg6mrk130 provenance
has publication info: NP69413.RAWilyFuCyPSndzh4jpQXIa7kS0N9P8UgKADFMwXg6mrk130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69413.RAWilyFuCyPSndzh4jpQXIa7kS0N9P8UgKADFMwXg6mrk130 assertion
type: Assertion
description: [Polymorphisms in genes involved in folate metabolism and colorectal neoplasia: a HuGE 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/14977639
was generated by: ECO_0000203

NP69414.RAfkiQK45gYKGiyID8ZoYCGEwQmac6TF6iWlwhNOpYi9Q
has assertion: NP69414.RAfkiQK45gYKGiyID8ZoYCGEwQmac6TF6iWlwhNOpYi9Q130 assertion
has provenance: NP69414.RAfkiQK45gYKGiyID8ZoYCGEwQmac6TF6iWlwhNOpYi9Q130 provenance
has publication info: NP69414.RAfkiQK45gYKGiyID8ZoYCGEwQmac6TF6iWlwhNOpYi9Q130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69414.RAfkiQK45gYKGiyID8ZoYCGEwQmac6TF6iWlwhNOpYi9Q130 assertion
type: Assertion
description: [The clinical importance of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism in the 5-fluoropyrimidine-based therapy of metastatic colorectal 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/15520876
was generated by: ECO_0000203

NP69420.RATeWYw0 60CeCJPgfMJTQg48eHR md-tgJbepm--W3eI
has assertion: NP69420.RATeWYw0 60CeCJPgfMJTQg48eHR md-tgJbepm--W3eI130 assertion
has provenance: NP69420.RATeWYw0 60CeCJPgfMJTQg48eHR md-tgJbepm--W3eI130 provenance
has publication info: NP69420.RATeWYw0 60CeCJPgfMJTQg48eHR md-tgJbepm--W3eI130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69420.RATeWYw0 60CeCJPgfMJTQg48eHR md-tgJbepm--W3eI130 assertion
type: Assertion
description: [Of six polymorphisms (677C>T-MTHFR, 1298A>C-MTHFR, 80G>A-RFC, 2756A>G-MS, 66A>G- MSR, 19bpDHFR and 1561C>T-GCPII), only 677C>T-MTHFR was a significant risk for hypertension: OR 1.89; 95% CI 1.07-3.32 (chi2 p = 0.038).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/19776634
was generated by: ECO_0000203

NP69421.RAXYoxc5utCs6MCs7wtUxf Yq0dk-ZcnibV4oBHu5L M
has assertion: NP69421.RAXYoxc5utCs6MCs7wtUxf Yq0dk-ZcnibV4oBHu5L M130 assertion
has provenance: NP69421.RAXYoxc5utCs6MCs7wtUxf Yq0dk-ZcnibV4oBHu5L M130 provenance
has publication info: NP69421.RAXYoxc5utCs6MCs7wtUxf Yq0dk-ZcnibV4oBHu5L M130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69421.RAXYoxc5utCs6MCs7wtUxf Yq0dk-ZcnibV4oBHu5L M130 assertion
type: Assertion
description: [Interactions between the single nucleotide polymorphisms in the homocysteine pathway (MTHFR 677C>T, MTHFR 1298 A>C, and CBSins) and the efficacy of HMG-CoA reductase inhibitors in preventing cardiovascular disease in high-risk patients of hypertension: the GenHAT 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/18622257
was generated by: ECO_0000203

NP69429.RARDhkCjiDYk2NTNCgMiiYVyQL1CTOSqFV4UdTF-QH3zE
has assertion: NP69429.RARDhkCjiDYk2NTNCgMiiYVyQL1CTOSqFV4UdTF-QH3zE130 assertion
has provenance: NP69429.RARDhkCjiDYk2NTNCgMiiYVyQL1CTOSqFV4UdTF-QH3zE130 provenance
has publication info: NP69429.RARDhkCjiDYk2NTNCgMiiYVyQL1CTOSqFV4UdTF-QH3zE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69429.RARDhkCjiDYk2NTNCgMiiYVyQL1CTOSqFV4UdTF-QH3zE130 assertion
type: Assertion
description: [The present study provides data on the folate, cobalamin, and homocysteine status of Spanish adolescents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18714149
was generated by: ECO_0000203

NP69431.RAVw1Gh1r6opHc hREDD81P5ziczVSeacyUiP53otIOqU
has assertion: NP69431.RAVw1Gh1r6opHc hREDD81P5ziczVSeacyUiP53otIOqU130 assertion
has provenance: NP69431.RAVw1Gh1r6opHc hREDD81P5ziczVSeacyUiP53otIOqU130 provenance
has publication info: NP69431.RAVw1Gh1r6opHc hREDD81P5ziczVSeacyUiP53otIOqU130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69431.RAVw1Gh1r6opHc hREDD81P5ziczVSeacyUiP53otIOqU130 assertion
type: Assertion
description: [These data show for the first time in humans that choline itself is a source of methyl groups for de novo PtdCho biosynthesis and indicate that the MTHFR 677TT genotype favors the use of choline as a methyl donor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21123458
was generated by: ECO_0000203

NP69433.RAfmPlJB55ETs4DiVbeKxr04LT80o3eVqQHYYk0rOD1-w
has assertion: NP69433.RAfmPlJB55ETs4DiVbeKxr04LT80o3eVqQHYYk0rOD1-w130 assertion
has provenance: NP69433.RAfmPlJB55ETs4DiVbeKxr04LT80o3eVqQHYYk0rOD1-w130 provenance
has publication info: NP69433.RAfmPlJB55ETs4DiVbeKxr04LT80o3eVqQHYYk0rOD1-w130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:32:33+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v2.1.0.0

NP69433.RAfmPlJB55ETs4DiVbeKxr04LT80o3eVqQHYYk0rOD1-w130 assertion
type: Assertion
description: [One may consider that a differential response of homocysteine to folic acid supplementation may depend on MTHFR genotype which may have important implications when attempting to lower homocysteine concentrations in populations with mild folate 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/14734201
was generated by: ECO_0000203