@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_head {
  this: np:hasAssertion dgn-np:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_assertion ;
    np:hasProvenance dgn-np:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_provenance ;
    np:hasPublicationInfo dgn-np:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_assertion a np:Assertion .
  dgn-np:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_provenance a np:Provenance .
  dgn-np:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_assertion {
  miriam-gene:3690 a ncit:C16612 .
  lld:C1842372 a ncit:C7057 .
  dgn-gda:DGNe1f5f6bbbec5be589f552d6dbda9600f sio:SIO_000628 miriam-gene:3690 , lld:C1842372 ;
    a sio:SIO_001122 .
}
dgn-np:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_provenance {
  dgn-np:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_assertion dcterms:description "[ Our results support the hypothesis that carriers of the PlA2 allele might have an increased risk for ACS. PlA2 homozygosity was associated with an inadequate response to aspirin therapy. Our data further suggest that patients with PlA2 allele homozygosit]. 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:15840736 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP70433.RA02kzjHRmolVXgGAV0OUT4IgJnQHBNxf2-EL6rU-UWwk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:18+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}