@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M> .
@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:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_head {
  this: np:hasAssertion dgn-np:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_assertion;
    np:hasProvenance dgn-np:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_provenance;
    np:hasPublicationInfo dgn-np:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_assertion a np:Assertion .
  
  dgn-np:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_provenance a np:Provenance .
  
  dgn-np:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_assertion {
  miriam-gene:6924 a ncit:C16612 .
  
  lld:C0206734 a ncit:C7057 .
  
  dgn-gda:DGN464a328791143f53e3492f6540483da9 sio:SIO_000628 miriam-gene:6924, lld:C0206734;
    a sio:SIO_001121 .
}

dgn-np:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_provenance {
  dgn-np:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_assertion dcterms:description
      "[The von Hippel-Lindau (VHL) tumour suppressorgene product is believed to be involved in the down-regulation of transcriptional elongation by preventing the association of elongin B and C with the catalytic subunit elongin A. Alterations in the human VHL gene lead to VHL disease which is associated with various rare neoplasias, including haemangioblastoma of the central nervous system, retinal angioma, clear cell renal carcinoma and pheochromocytoma.]. 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:9931330;
    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:NP508229.RARRDE4q-SyewsCB9kCGI7ThIUrMMdZ8QRMQNRS_JIW0M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:03+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" .
}