@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_head {
  this: np:hasAssertion dgn-np:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_assertion;
    np:hasProvenance dgn-np:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_provenance;
    np:hasPublicationInfo dgn-np:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_assertion a np:Assertion .
  
  dgn-np:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_provenance a np:Provenance .
  
  dgn-np:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGNe453bd097f4d0de9eef60711f8e25cea sio:SIO_000628 miriam-gene:7428, lld:C0596263;
    a sio:SIO_001121 .
}

dgn-np:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_provenance {
  dgn-np:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_assertion dcterms:description
      "[Detection of VHL gene alterations using these accurate, sensitive, and practical methods provides evidence that the vast majority of histologically confirmed ccRCC tumors possess genetic or epigenetic alteration of the VHL gene and support the hypothesis that VHL alteration is an early event in ccRCC carcinogenesis.]. 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:18676741;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP403332.RAsu3vd_tkjVMQRjUPeqwJ91tP3GITCqgOsh6eS4gE05g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:00+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}