@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ> .
@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:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_head {
  this: np:hasAssertion dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_assertion;
    np:hasProvenance dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_provenance;
    np:hasPublicationInfo dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_assertion a np:Assertion .
  
  dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_provenance a np:Provenance .
  
  dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_assertion {
  miriam-gene:2146 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGNfc8a1d762c941a86dae09a7cf4f40f9b sio:SIO_000628 miriam-gene:2146, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_provenance {
  dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_assertion dct:description
      "[ We have possibly identified haplotypes which mark alleles that have a beneficial effect on the development of prostate cancer. Moreover, our results suggest that genetic variations of the EZH2 gene are not responsible for the linkage of 7q to aggressive 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:16015586;
    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:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+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" .
}