@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw> .
@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:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_head {
  this: np:hasAssertion dgn-np:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_assertion;
    np:hasProvenance dgn-np:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_provenance;
    np:hasPublicationInfo dgn-np:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_assertion a np:Assertion .
  
  dgn-np:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_provenance a np:Provenance .
  
  dgn-np:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_assertion {
  miriam-gene:1586 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
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dgn-np:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_provenance {
  dgn-np:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_assertion dcterms:description
      "[We genotyped 23 haplotype tagging single nucleotide polymorphisms in the genes AR, CYP17, and SRD5A2 and used Cox proportional hazards analyses to quantify associations between genotype and risk of dying from 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:17785571;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP182106.RAU0VVQIyLKPuMXgCggt24sBrOaWcqrvLRywTlHg9nUXw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}