@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88> .
@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:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_head {
  this: np:hasAssertion dgn-np:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_assertion;
    np:hasProvenance dgn-np:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_provenance;
    np:hasPublicationInfo dgn-np:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_assertion a np:Assertion .
  
  dgn-np:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_provenance a np:Provenance .
  
  dgn-np:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_assertion {
  miriam-gene:1071 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGNe3ae38654f63c62f711d9011c42fc24d sio:SIO_000628 miriam-gene:1071, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_provenance {
  dgn-np:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_assertion dcterms:description
      "[The inhibition of CETP can lead to substantial elevations in HDL-C. Based on a number of considerations, including the complex relationship between loss of function mutations in CETP and risk for CAD and the clinical experience with torcetrapib, it is difficult to predict if CETP inhibition will be associated with reductions in rates of atherosclerosis disease progression and risk for cardiovascular 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:21909703;
    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:NP229056.RAQaCJyDgnDW2CTzcAf6816KM3y5FcV_gbHaV9DYG4H88130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:08+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" .
}