@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY> .
@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:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_head {
   this: np:hasAssertion dgn-np:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_assertion ;
    np:hasProvenance dgn-np:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_provenance ;
    np:hasPublicationInfo dgn-np:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_assertion a np:Assertion .
  dgn-np:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_provenance a np:Provenance .
  dgn-np:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_assertion {
   miriam-gene:7428 a ncit:C16612 .
  lld:C0238463 a ncit:C7057 .
  dgn-gda:DGN6f21611120d6d3dc452d80ff62c929e0 sio:SIO_000628 miriam-gene:7428 , lld:C0238463 ;
    a sio:SIO_001121 .
}
dgn-np:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_provenance {
   dgn-np:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_assertion dcterms:description "[Alterations of the von Hippel-Lindau (VHL) tumor suppressor gene can cause different hereditary tumors associated with VHL syndrome, but the potential role of the VHL gene in papillary thyroid carcinoma (PTC) has not been characterized.]. 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:25490036 ;
    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:NP1246408.RAWAKCXJPqGt20tjzU0P4hGNwSHv2cTDW0t4nKQpyfpsY130_publicationInfo {
   this: dcterms:created "2016-05-13T12:51:11+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" .
}