@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc> .
@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:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_head {
  this: np:hasAssertion dgn-np:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_assertion;
    np:hasProvenance dgn-np:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_provenance;
    np:hasPublicationInfo dgn-np:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_assertion a np:Assertion .
  
  dgn-np:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_provenance a np:Provenance .
  
  dgn-np:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_assertion {
  miriam-gene:133482 a ncit:C16612 .
  
  lld:C1458156 a ncit:C7057 .
  
  dgn-gda:DGN5645cae1cae9a5c8bb8155b92890d9d0 sio:SIO_000628 miriam-gene:133482, lld:C1458156;
    a sio:SIO_001121 .
}

dgn-np:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_provenance {
  dgn-np:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_assertion dcterms:description
      "[Although the GSTM1 null genotype has been shown to increase prostate cancer mortality in Caucasians, potential associations between GST polymorphisms and prostate cancer biochemical recurrence (BCR) have not been well studied, particularly in African-Americans.]. 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:19568698;
    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:NP864455.RAc7AMd7N1Ujb5eMf2VOXDFJDXFUMcOdlKx7f_6EKUHnc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:48+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" .
}