@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY> .
@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:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_head {
  this: np:hasAssertion dgn-np:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_assertion;
    np:hasProvenance dgn-np:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_provenance;
    np:hasPublicationInfo dgn-np:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_assertion a np:Assertion .
  
  dgn-np:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_provenance a np:Provenance .
  
  dgn-np:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGNd97604b4ef2757b8a697af4873d5dd83 sio:SIO_000628 miriam-gene:7428, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_provenance {
  dgn-np:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_assertion dcterms:description
      "[The majority of conventional or clear cell renal carcinomas are associated with losses of chromosome 3p and mutation in the von Hippel Lindau (VHL) gene which is located on that portion of the genome.]. 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:9666053;
    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:NP440005.RABK2KLNLXiH-jMEnlKUdW8YuoanbBwq032JaFAxPBpyY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:20+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" .
}