@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ> .
@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:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_head {
  this: np:hasAssertion dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_assertion;
    np:hasProvenance dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_provenance;
    np:hasPublicationInfo dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_assertion a np:Assertion .
  
  dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_provenance a np:Provenance .
  
  dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_assertion {
  miriam-gene:65125 a ncit:C16612 .
  
  lld:C0220666 a ncit:C7057 .
  
  dgn-gda:DGN5573c3f40527c8a937d67988d85bcc14 sio:SIO_000628 miriam-gene:65125, lld:C0220666;
    a sio:SIO_001121 .
}

dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_provenance {
  dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_assertion dcterms:description
      "[This finding of association between a SNP near the promoter region and the severity of hypertension suggests that increased expression of WNK1 might contribute to BP variability and susceptibility to EH similar to the mechanism of hypertension observed in Gordon's syndrome.]. 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:15888480;
    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:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:38+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" .
}