@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE> .
@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:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_head {
  this: np:hasAssertion dgn-np:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_assertion;
    np:hasProvenance dgn-np:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_provenance;
    np:hasPublicationInfo dgn-np:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_assertion a np:Assertion .
  
  dgn-np:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_provenance a np:Provenance .
  
  dgn-np:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN609cc27d15fdb273e1253fac8a8224a2 sio:SIO_000628 miriam-gene:7421, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_provenance {
  dgn-np:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_assertion dcterms:description
      "[The purpose of this study was to analyse the frequency and type of mutations in the coding region of androgen receptor (AR) and to determine the role of polymorphisms in the intron 1 of ERalpha, exon 5 of ERbeta, intron 7 of progesterone, exon 7 of the aromatase (CYP19) and exon 9 of VDR genes in the risk of prostate cancer.]. 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:18483761;
    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:NP58987.RAqpnkL5h3rqDl_FkQi0C77p2w6c1z6SibMeYvgVHLItE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}