@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk> .
@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:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_head {
  this: np:hasAssertion dgn-np:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_assertion;
    np:hasProvenance dgn-np:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_provenance;
    np:hasPublicationInfo dgn-np:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_assertion a np:Assertion .
  
  dgn-np:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_provenance a np:Provenance .
  
  dgn-np:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_assertion {
  miriam-gene:1543 a ncit:C16612 .
  
  lld:C0948089 a ncit:C7057 .
  
  dgn-gda:DGNf742d4d98c22025763ed8d24c3b4a114 sio:SIO_000628 miriam-gene:1543, lld:C0948089;
    a sio:SIO_001122 .
}

dgn-np:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_provenance {
  dgn-np:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_assertion dcterms:description
      "[The results indicate that the homozygous CYP1A1 6235C genotype is associated with greater mortality following the onset of ACS, independent of ethnicity and clinical risk factors, but related to smoking history.]. 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:19650794;
    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:NP76652.RA221zgLkc2_0a5SIyIQpgaHe-8f3n59yXU-oimM6y0Xk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:37+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" .
}