@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo> .
@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:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_head {
  this: np:hasAssertion dgn-np:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_assertion;
    np:hasProvenance dgn-np:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_provenance;
    np:hasPublicationInfo dgn-np:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_assertion a np:Assertion .
  
  dgn-np:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_provenance a np:Provenance .
  
  dgn-np:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_assertion {
  miriam-gene:6045 a ncit:C16612 .
  
  lld:C1306459 a ncit:C7057 .
  
  dgn-gda:DGNc2abf9e3f651c435479d1b63c5f24aab sio:SIO_000628 miriam-gene:6045, lld:C1306459;
    a sio:SIO_001121 .
}

dgn-np:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_provenance {
  dgn-np:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_assertion dcterms:description
      "[In addition, a review of BAP1 cancer syndrome families reported to date indicates that the location of the BAP1 mutation does not have any bearing on the spectrum of cancer types observed, either for mesothelial or melanocytic tumors.]. 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:23849051;
    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:NP673151.RATKFAjSPEaFGAKmRGDJTLYZR9V_Z45I0cVBMktdcRiGo130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:24+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" .
}