@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_head {
  this: np:hasAssertion dgn-np:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_assertion;
    np:hasProvenance dgn-np:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_provenance;
    np:hasPublicationInfo dgn-np:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_assertion a np:Assertion .
  
  dgn-np:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_provenance a np:Provenance .
  
  dgn-np:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_assertion {
  miriam-gene:847 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNbb25ec5a08d1f3c6e2ee15719f75f0e8 sio:SIO_000628 miriam-gene:847, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_provenance {
  dgn-np:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_assertion dcterms:description
      "[Our data suggest that genetic variations in the promoter region of catalase gene influence the susceptibility to essential hypertension. In addition, the genetic factors that contribute to hypertension maybe different between ethnic groups.]. 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:15735318;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP57661.RAFNhdg2P1kkJadG6LrPteb955HCm60FuMW5imomV9Hic130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:11+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}