@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY> .
@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 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:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_head {
  this: np:hasAssertion dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_assertion ;
    np:hasProvenance dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_provenance ;
    np:hasPublicationInfo dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_assertion a np:Assertion .
  dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_provenance a np:Provenance .
  dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  lld:C0740457 a ncit:C7057 .
  dgn-gda:DGN56966a7b19a15b548add54126edfceb3 sio:SIO_000628 miriam-gene:7428 , lld:C0740457 ;
    a sio:SIO_001122 .
}
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_provenance {
  dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_assertion dct:description "[ In this study non-significantly increased risks for history of hypertension and use of antihypertensive medication with RCC were observed. The association with hypertension was stronger in RCC patients with VHL mutations, while there was a positive association of diuretics use and risk of RCC without VHL mutations.]. 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:16208141 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}