@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII> .
@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:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_head {
  this: np:hasAssertion dgn-np:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_assertion;
    np:hasProvenance dgn-np:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_provenance;
    np:hasPublicationInfo dgn-np:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_assertion a np:Assertion .
  
  dgn-np:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_provenance a np:Provenance .
  
  dgn-np:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_assertion {
  miriam-gene:9223 a ncit:C16612 .
  
  lld:C0740457 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_provenance {
  dgn-np:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_assertion dcterms:description
      "[Herein, I review the evidence that implicated PBRM1 and BAP1 as renal cancer driver genes, provide an update on the function of the gene products, and speculate on how mutations in these genes may be exploited therapeutically.]. 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:23867514;
    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:NP307400.RApchezGQBIClZOw6MYTDviLnca7vZOTq9moGP0q88KII130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:56+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" .
}