@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4> .
@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:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_head {
  this: np:hasAssertion dgn-np:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_assertion;
    np:hasProvenance dgn-np:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_provenance;
    np:hasPublicationInfo dgn-np:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_assertion a np:Assertion .
  
  dgn-np:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_provenance a np:Provenance .
  
  dgn-np:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_assertion {
  miriam-gene:79811 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGNe0b1c99e72138c6d32c6c4b0c1cc4224 sio:SIO_000628 miriam-gene:79811, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_provenance {
  dgn-np:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_assertion dcterms:description
      "[Investigation of rare familial forms of renal cell carcinoma (RCC) has led to the identification of genes such as VHL and MET that are also implicated in the pathogenesis of sporadic RCC.]. 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:24000165;
    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:NP945750.RAnhy5an7m0dgKl3ppy-M7GcaFHOv_cCT8Ntn2smz6HN4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:17+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" .
}