@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA> .
@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:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_head {
  this: np:hasAssertion dgn-np:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_assertion;
    np:hasProvenance dgn-np:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_provenance;
    np:hasPublicationInfo dgn-np:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_assertion a np:Assertion .
  
  dgn-np:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_provenance a np:Provenance .
  
  dgn-np:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_assertion {
  miriam-gene:342977 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN8ab3fdd1207dc7e3384079d3398392d6 sio:SIO_000628 miriam-gene:342977, lld:C1956346;
    a sio:SIO_001121 .
}

dgn-np:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_provenance {
  dgn-np:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_assertion dcterms:description
      "[The presence of NOS3 T allele was not associated with the risk of CAD or T2DM, and the CETP B1 allele was only significantly associated with the increased risk of CAD in total CAD patients (odds ratio (OR) = 5.1, p = 0.019).]. 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:23157875;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP720576.RATmDwFO7iv6a6AaiyUV7OOJ7uaw4OQAmzfc3ILtOBFVA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:17+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" .
}