@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c> .
@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:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_head {
  this: np:hasAssertion dgn-np:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_assertion;
    np:hasProvenance dgn-np:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_provenance;
    np:hasPublicationInfo dgn-np:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_assertion a np:Assertion .
  
  dgn-np:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_provenance a np:Provenance .
  
  dgn-np:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGN6774c1f96fa9b61ae246dab48225be82 sio:SIO_000628 miriam-gene:7428, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_provenance {
  dgn-np:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_assertion dcterms:description
      "[Somatic inactivation of the VHL gene is the main molecular event in most sporadic RCC and the treatment of advanced RCC has been revolutionized by targeted therapy with drugs that block angiogenesis.]. 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:22659535;
    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:NP773529.RAlNj9GkOP7CO4C-oDi5msfB2p2K2ZjxSMxINu4eTq4-c130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:27+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" .
}