@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8> .
@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:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_head {
  this: np:hasAssertion dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_assertion ;
    np:hasProvenance dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_provenance ;
    np:hasPublicationInfo dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_assertion a np:Assertion .
  dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_provenance a np:Provenance .
  dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  lld:C0019562 a ncit:C7057 .
  dgn-gda:DGN250870d2c5d5029642a9a3951a42b200 sio:SIO_000628 miriam-gene:2272 , lld:C0019562 ;
    a sio:SIO_001121 .
}
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_provenance {
  dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_assertion dcterms:description "[Here we show that the von Hippel-Lindau (VHL) tumour suppressor protein, pVHL, which is inactivated in hereditary and sporadic forms of renal cell carcinoma, localizes to the mitotic spindle in mammalian cells and its functional inactivation provokes spindle misorientation, spindle checkpoint weakening and chromosomal instability.]. 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:19620968 ;
    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:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:06+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" .
}