@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug> .
@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:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_head {
  this: np:hasAssertion dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_assertion ;
    np:hasProvenance dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_provenance ;
    np:hasPublicationInfo dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_assertion a np:Assertion .
  dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_provenance a np:Provenance .
  dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_assertion {
  miriam-gene:65266 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGN5d1b1690574ca2ece144199b91f8999e sio:SIO_000628 miriam-gene:65266 , lld:C0020538 ;
    a sio:SIO_001122 .
}
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_provenance {
  dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_assertion dcterms:description "[No significant differences in allelic or genotypic frequencies were observed in African Americans for any SNPs. The finding in whites is consistent with the hypothesis that polymorphisms in WNK4 influence the risk of hypertension. However, because the associated SNP does not appear to be a functional variant and the limitations of case/control association studies, confirmation of these results in additional cohorts is warranted.]. 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:12719438 ;
    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:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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: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" .
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}