@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_head {
  this: np:hasAssertion dgn-np:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_assertion;
    np:hasProvenance dgn-np:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_provenance;
    np:hasPublicationInfo dgn-np:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_assertion a np:Assertion .
  
  dgn-np:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_provenance a np:Provenance .
  
  dgn-np:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN6f7b5215a62ab263c0e28fae4163282f sio:SIO_000628 miriam-gene:367, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_provenance {
  dgn-np:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_assertion dcterms:description
      "[These results offer general import beyond prostate cancer, given that nuclear FHL2 is characteristic of other human cancers where oncogenic transcription factors that drive disease are activated like the AR in 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:23801747;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP249903.RATncDIxAE46LaTfCSRiaMF6Hx2w8gSrtMftHBHmh6ytE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:02+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}