@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA> .
@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 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:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_head {
   this: np:hasAssertion dgn-np:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_assertion ;
    np:hasProvenance dgn-np:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_provenance ;
    np:hasPublicationInfo dgn-np:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_assertion a np:Assertion .
  dgn-np:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_provenance a np:Provenance .
  dgn-np:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_assertion {
   miriam-gene:3293 a ncit:C16612 .
  lld:C0376358 a ncit:C7057 .
  dgn-gda:DGNdbe267a7bd1e6a18c4527c2af15677b3 sio:SIO_000628 miriam-gene:3293 , lld:C0376358 ;
    a sio:SIO_001122 .
}
dgn-np:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_provenance {
   dgn-np:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_assertion dct:description "[To estimate the prostate cancer risk conferred by individual single nucleotide polymorphisms (SNPs), SNP-SNP interactions, and/or cumulative SNP effects, we evaluated the association between prostate cancer risk and the genetic variants of 12 key genes within the steroid hormone pathway (CYP17, HSD17B3, ESR1, SRD5A2, HSD3B1, HSD3B2, CYP19, CYP1A1, CYP1B1, CYP3A4, CYP27B1, and CYP24A1).]. 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:19505920 ;
    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:NP57509.RAxs6S2dQo88I0EdtawaBWRTzNIgBlotKjVDMV0MUDYkA130_publicationInfo {
   this: dct:created "2014-10-02T12:32:27+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}