@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA> .
@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:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_head {
  this: np:hasAssertion dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_assertion ;
    np:hasProvenance dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_provenance ;
    np:hasPublicationInfo dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_assertion a np:Assertion .
  dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_provenance a np:Provenance .
  dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  lld:C0027651 a ncit:C7057 .
  dgn-gda:DGNfde1f88f51eeca9ac5b638fa695386c4 sio:SIO_000628 miriam-gene:7428 , lld:C0027651 ;
    a sio:SIO_001121 .
}
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_provenance {
  dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_assertion dcterms:description "[Even preneoplastic cystic structures may harbor entire loss of the chromosome 3, suggesting that loss of VHL gene function alone is not immediately causative for neoplastic growth, but further events, either mutations and deletions in other chromosomes or epigenetic or other than genetic phenomena, are required for tumor formation.]. 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:16261628 ;
    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:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:57+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" .
}