@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A> .
@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:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_head {
  this: np:hasAssertion dgn-np:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_assertion;
    np:hasProvenance dgn-np:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_provenance;
    np:hasPublicationInfo dgn-np:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_assertion a np:Assertion .
  
  dgn-np:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_provenance a np:Provenance .
  
  dgn-np:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_assertion {
  miriam-gene:1071 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGN6d07fef2fffb9d49a1975f0d1e58b8a6 sio:SIO_000628 miriam-gene:1071, lld:C0010054;
    a sio:SIO_001122 .
}

dgn-np:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_provenance {
  dgn-np:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_assertion dcterms:description
      "[To understand further the role that CETP gene plays in the pathogenesis of coronary heart disease (CHD), the promoter region, all 16 exons and adjacent intronic regions of CETP gene were screened for single nucleotide polymorphisms (SNPs) in 203 CHD patients and 209 healthy volunteers by the combination of PCR, denaturing high performance liquid chromatography (DHPLC), molecular cloning, and DNA sequencing.]. 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:14732872;
    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:NP46915.RA50wV-WgtDXhpdARqiZJfnHB3bk9MHlUTDEIBZG-m0_A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}