@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_head
{
this:
np:hasAssertion
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_assertion
;
np:hasProvenance
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_assertion
a
np:Assertion
.
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_provenance
a
np:Provenance
.
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_assertion
{
miriam-gene:4988
a
ncit:C16612
.
lld:C0600241
a
ncit:C7057
.
dgn-gda:DGN2f87a7783ecdfdbe239e4b9060fe763a
sio:SIO_000628
miriam-gene:4988
,
lld:C0600241
;
a
sio:SIO_001122
.
}
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_provenance
{
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_assertion
dcterms:description
"[For the A118G polymorphism, we found significant differences in allele and genotype frequencies between different ethnic groups and highly significant association with heroin dependence in Indians for both genotype distribution (p = 0.024) and allele frequency (p = 0.009). For the C17 T polymorphism, the minor allele was documented in Chinese and Malays for the first time. Molecular haplotyping revealed complete linkage dis-equilibrium between the A118G and C17 T polymorphisms. Linkage disequilibrium between the A118G and C1031G polymorphisms was found to be almost complete in all four ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:12657887
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP53460.RAAPFOToml9rd5r-hgZJg_p5byr98f-lOa8QBmiLsbgZQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}