@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_head {
  this: np:hasAssertion dgn-np:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_assertion;
    np:hasProvenance dgn-np:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_provenance;
    np:hasPublicationInfo dgn-np:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_assertion a np:Assertion .
  
  dgn-np:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_provenance a np:Provenance .
  
  dgn-np:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGN87128e604aba9f6499a3485f86818334 sio:SIO_000628 miriam-gene:7428, lld:C0596263;
    a sio:SIO_001121 .
}

dgn-np:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_provenance {
  dgn-np:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_assertion dcterms:description
      "[These mutations may cause substitutions of specific amino acid residue and functional change of VHL protein (pVHL), which leads to the oncogenesis of the particular tumor types that characterize the different VHL disease types.]. 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:15870918;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP493195.RAFRgF6FehFM_r2z48vpawKco5uGboYh4VuC5Mc2mL_3s130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:28+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}