@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o> .
@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/v3.0.0/void/> .
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_head {
  this: np:hasAssertion dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_assertion ;
    np:hasProvenance dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_provenance ;
    np:hasPublicationInfo dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_assertion a np:Assertion .
  dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_provenance a np:Provenance .
  dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  lld:C2931852 a ncit:C7057 .
  dgn-gda:DGN2acd0a1c5bd1e7244869a1105d0ac885 sio:SIO_000628 miriam-gene:7428 , lld:C2931852 ;
    a sio:SIO_001121 .
}
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_provenance {
  dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_assertion dcterms:description "[Taken together, CAIX expression and VHL mutational status are able to stratify patients with clear cell RCC into distinct groups with regards to clinicopathological variables and prognosis, with low CAIX expression and absence of VHL mutation being associated with a poor clinicopathological phenotype and diminished survival.]. 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:18464292 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:28+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}