@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE> .
@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:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_head {
  this: np:hasAssertion dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_assertion;
    np:hasProvenance dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_provenance;
    np:hasPublicationInfo dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_assertion a np:Assertion .
  
  dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_provenance a np:Provenance .
  
  dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_assertion {
  miriam-gene:2053 a ncit:C16612 .
  
  lld:C3272363 a ncit:C7057 .
  
  dgn-gda:DGN861033ca0b34269daebf75a384d25b1e sio:SIO_000628 miriam-gene:2053, lld:C3272363;
    a sio:SIO_001121 .
}

dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_provenance {
  dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_assertion dcterms: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;
    sio: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:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:47+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" .
}