@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs> .
@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:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_head {
  this: np:hasAssertion dgn-np:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_assertion;
    np:hasProvenance dgn-np:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_provenance;
    np:hasPublicationInfo dgn-np:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_assertion a np:Assertion .
  
  dgn-np:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_provenance a np:Provenance .
  
  dgn-np:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_assertion {
  miriam-gene:4233 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGNcbe170c66cf786a4d17f8c01db2dea6b sio:SIO_000628 miriam-gene:4233, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_provenance {
  dgn-np:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_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:NP553917.RArtYtONWPQ2AHXknuVdb0eNbN_3zECetYScNqAMYUMWs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:08+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" .
}