@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM> .
@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:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_head {
  this: np:hasAssertion dgn-np:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_assertion;
    np:hasProvenance dgn-np:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_provenance;
    np:hasPublicationInfo dgn-np:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_assertion a np:Assertion .
  
  dgn-np:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_provenance a np:Provenance .
  
  dgn-np:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_assertion {
  miriam-gene:65125 a ncit:C16612 .
  
  lld:C0085580 a ncit:C7057 .
  
  dgn-gda:DGN6524cb7d2eaa8843af0f44a760f944d1 sio:SIO_000628 miriam-gene:65125, lld:C0085580;
    a sio:SIO_001122 .
}

dgn-np:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_provenance {
  dgn-np:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_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: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:NP59283.RAiUU6u4lug2DIIBUQmmBn5XnIRTNU3Ne0UN6AoNAabaM130_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" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}