@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg> .
@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 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:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_head {
  this: np:hasAssertion dgn-np:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_assertion;
    np:hasProvenance dgn-np:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_provenance;
    np:hasPublicationInfo dgn-np:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_assertion a np:Assertion .
  
  dgn-np:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_provenance a np:Provenance .
  
  dgn-np:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_assertion {
  miriam-gene:3690 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGNafd5ca34e19ee1f2274524b5818e71be sio:SIO_000628 miriam-gene:3690, lld:C0027051;
    a sio:SIO_001122 .
}

dgn-np:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_provenance {
  dgn-np:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_assertion dcterms:description
      "[Our results indicated that the distributions of some hemostatic genetic polymorphisms between Asians and Caucasians were significantly different. In a group of young patients suviving their first myocardial infarction, some genetic factors might influence the prognosis after myocardial infarction. Such information is valuable for risk stratification in patients with myocardial infarction.]. 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:12362250;
    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:NP55691.RA9Emwq1dSRMPxJrsSiEgpeu0NDMDl7kuOGhft6Us3Acg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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 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" .
}