@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I> .
@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:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_head {
  this: np:hasAssertion dgn-np:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_assertion;
    np:hasProvenance dgn-np:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_provenance;
    np:hasPublicationInfo dgn-np:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_assertion a np:Assertion .
  
  dgn-np:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_provenance a np:Provenance .
  
  dgn-np:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  
  lld:C2930839 a ncit:C7057 .
  
  dgn-gda:DGN0cfe4a84f2292fb4017702b57dfdbb75 sio:SIO_000628 miriam-gene:7428, lld:C2930839;
    a sio:SIO_001121 .
}

dgn-np:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_provenance {
  dgn-np:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_assertion dcterms:description
      "[Results to date suggest that a substantial proportion of patients with familial pheochromocytoma have VHL gene mutations but in contrast, most familial clusters of clear cell renal cell carcinoma (RCC) without evidence of VHL do not have germline VHL mutations.]. 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:9681854;
    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:NP798067.RAQHcW9UKJSVC6jP3m09fMyM-bKKbvrwUfMrJQfb2lr0I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:10+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" .
}