@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI> .
@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:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_head {
  this: np:hasAssertion dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_assertion;
    np:hasProvenance dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_provenance;
    np:hasPublicationInfo dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_assertion a np:Assertion .
  
  dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_provenance a np:Provenance .
  
  dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_assertion {
  miriam-gene:3162 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN6224af4ce74f9811e26ab316c8521efa sio:SIO_000628 miriam-gene:3162, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_provenance {
  dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_assertion dcterms:description
      "[ The AA genotype of HMOX-1 is associated with an increased incidence of hypertension in women. Oestrogen attenuates vasoconstriction by increasing the expression of inducible nitric oxide synthase. As carbon monoxide, which is one of the products of HO-1, can attenuate nitric oxide-induced vasodilatation, a high expression of HO-1 may cause hypertension, especially in women.]. 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:12872043;
    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:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}