@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk> .
@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:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_head {
  this: np:hasAssertion dgn-np:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_assertion ;
    np:hasProvenance dgn-np:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_provenance ;
    np:hasPublicationInfo dgn-np:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_assertion a np:Assertion .
  dgn-np:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_provenance a np:Provenance .
  dgn-np:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_assertion {
  miriam-gene:2271 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
  dgn-gda:DGN7e2523f8e73df0d03a890629e39ea517 sio:SIO_000628 miriam-gene:2271 , lld:C0007097 ;
    a sio:SIO_001121 .
}
dgn-np:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_provenance {
  dgn-np:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_assertion dcterms:description "[Generalized cellular hypoxia (in sickle cell disease) or pseudohypoxia (in tumors with fumarate hydratase and von Hippel-Lindau mutations or epigenetic silencing) may act alone or in concert at the level of medullary tubular epithelium to promote development of this rare type of renal carcinoma, which could then be genetically reclassified as either fumarate hydratase-associated renal carcinomas or high-grade clear cell renal cell carcinomas.]. 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:21733559 ;
    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:NP484751.RARyMCickbxeezQbaVY9pJu2yMVMsRybyLbzHd2Dy2igk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:50+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" .
}