@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM> .
@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:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_head {
  this: np:hasAssertion dgn-np:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_assertion;
    np:hasProvenance dgn-np:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_provenance;
    np:hasPublicationInfo dgn-np:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_assertion a np:Assertion .
  
  dgn-np:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_provenance a np:Provenance .
  
  dgn-np:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_assertion {
  miriam-gene:1284 a ncit:C16612 .
  
  lld:C0342649 a ncit:C7057 .
  
  dgn-gda:DGN30fc863f4b98e28eef5b050941671f5e sio:SIO_000628 miriam-gene:1284, lld:C0342649;
    a sio:SIO_001122 .
}

dgn-np:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_provenance {
  dgn-np:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_assertion dcterms:description
      "[SNPs in the 9p21 and PHACTR1 gene loci were strongly associated with CAC and MI, and there are suggestive associations with both CAC and MI of SNPs in additional loci. Multiple genetic loci are associated with development of both underlying coronary atherosclerosis and clinical events.]. 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:22144573;
    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:NP96659.RABZJ-aF00Wvw8yfq0cO5hCZEGvkGGI_2VEuUmRi6UdtM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:49+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" .
}