@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM> .
@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:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_head {
  this: np:hasAssertion dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_assertion;
    np:hasProvenance dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_provenance;
    np:hasPublicationInfo dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_assertion a np:Assertion .
  
  dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_provenance a np:Provenance .
  
  dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_assertion {
  miriam-gene:51206 a ncit:C16612 .
  
  lld:C0019080 a ncit:C7057 .
  
  dgn-gda:DGN41c76bb770203044da50e050ce88f1f2 sio:SIO_000628 miriam-gene:51206, lld:C0019080;
    a sio:SIO_001122 .
}

dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_provenance {
  dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_assertion dcterms:description
      "[Cyclooxygenase-1 -842G and 50T alleles significantly contribute to the risk of bleeding complications in patients undergoing elective CAG. Genetic testing is able to influence the safety of diagnostic cardiac catheterization in large numbers of low risk patients with borderline indications.]. 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:20691446;
    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:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:45+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" .
}