@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE> .
@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:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_head {
  this: np:hasAssertion dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_assertion ;
    np:hasProvenance dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_provenance ;
    np:hasPublicationInfo dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_assertion a np:Assertion .
  dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_provenance a np:Provenance .
  dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_assertion {
  miriam-gene:768 a ncit:C16612 .
  lld:C2931852 a ncit:C7057 .
  dgn-gda:DGN2ba1d3c6c8ed53f1c1a899bde7ebeba1 sio:SIO_000628 miriam-gene:768 , lld:C2931852 ;
    a sio:SIO_001121 .
}
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_provenance {
  dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_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-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:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:44+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" .
}