@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk> .
@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 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:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_head {
  this: np:hasAssertion dgn-np:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_assertion;
    np:hasProvenance dgn-np:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_provenance;
    np:hasPublicationInfo dgn-np:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_assertion a np:Assertion .
  
  dgn-np:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_provenance a np:Provenance .
  
  dgn-np:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_assertion {
  miriam-gene:1071 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGN3f9a1455fcd076eee980a9f147f86377 sio:SIO_000628 miriam-gene:1071, lld:C0010054;
    a sio:SIO_001122 .
}

dgn-np:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_provenance {
  dgn-np:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_assertion dct:description
      "[To determine the frequencies of 4 mutations of cholesteryl ester transfer protein (CETP) gene in Chinese population and to investigate the association of the mutations with lipid metabolism and the susceptibility to coronary atherosclerotic heart disease (CHD).]. 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:12579494;
    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:NP46914.RApvT5TcbgR74_q8LJw_9tK2uSCz-24a_JaOie6ZdzKLk130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}