@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc> .
@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:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_head {
  this: np:hasAssertion dgn-np:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_assertion;
    np:hasProvenance dgn-np:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_provenance;
    np:hasPublicationInfo dgn-np:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_assertion a np:Assertion .
  
  dgn-np:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_provenance a np:Provenance .
  
  dgn-np:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_assertion {
  miriam-gene:5104 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN6d977feede65fa63b50d76a841e83a82 sio:SIO_000628 miriam-gene:5104, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_provenance {
  dgn-np:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_assertion dcterms:description
      "[The results of the present study indicate that the EPHX2 K55R polymorphism is not associated with restenosis after PCI, with incidence of CHD, or with an increased risk of hypertension and therefore, can not serve as a predictor for risk of CHD or restenosis after PCI.]. 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:19814804;
    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:NP897924.RAUN0pY-7BiSx5cdeD75dN5IHHOtiuuNazKxu7q1ViRSc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:12+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" .
}