@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM> .
@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:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_head {
  this: np:hasAssertion dgn-np:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_assertion;
    np:hasProvenance dgn-np:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_provenance;
    np:hasPublicationInfo dgn-np:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_assertion a np:Assertion .
  
  dgn-np:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_provenance a np:Provenance .
  
  dgn-np:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_assertion {
  miriam-gene:345 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN0bd4d816f4ec8fc1654a061eaa3a1722 sio:SIO_000628 miriam-gene:345, lld:C1956346;
    a sio:SIO_001121 .
}

dgn-np:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_provenance {
  dgn-np:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_assertion dcterms:description
      "[We aimed to investigate the possible associations between LPL gene and apolipoprotein C3 (APOC3) gene polymorphisms with coronary artery disease (CAD) and its severity, as well as the interaction between these polymorphisms and classical risk factors.]. 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:23377670;
    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:NP262293.RAu65tbsvbxOZE-Ap9wVEb3i99XetkGUG2MyBOWfNtuPM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}