@prefix semsc: <http://semanticscience.org/resource/> .
@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@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 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:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_head {
  this: np:hasAssertion dgn-np:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_assertion;
    np:hasProvenance dgn-np:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_provenance;
    np:hasPublicationInfo dgn-np:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_assertion a np:Assertion .
  
  dgn-np:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_provenance a np:Provenance .
  
  dgn-np:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_assertion {
  miriam-gene:2053 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGNbd0c0793e8521acbd1cf950093dbb13c semsc:SIO_000628 miriam-gene:2053, lld:C0007222;
    a semsc:SIO_001121 .
}

dgn-np:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_provenance {
  dgn-np:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_assertion dct:description
      "[This suggests that the relationship between the EPHX2 gene and risk of ischemic stroke and other cardiovascular disease does not exist or its effect size is likely to be quite small.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    semsc:SIO_000772 miriam-pubmed:19940276;
    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:NP205879.RAAmqwyTYAZWYPisfH0r9jAuJgN77C8Si0jDH48G-tQ7o130_publicationInfo {
  this: dct:created "2014-10-02T12:33:53+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject semsc:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}