@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI> .
@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:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_head {
  this: np:hasAssertion dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_assertion;
    np:hasProvenance dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_provenance;
    np:hasPublicationInfo dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_assertion a np:Assertion .
  
  dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_provenance a np:Provenance .
  
  dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_assertion {
  miriam-gene:1071 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGN7ef94c2ad35ce827bff320fd325e3950 sio:SIO_000628 miriam-gene:1071, lld:C0027051;
    a sio:SIO_001122 .
}

dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_provenance {
  dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_assertion dcterms:description
      "[These results strongly confirm the role of the CETP gene and the TaqIB variant as a risk factor for MI and suggest that another functional polymorphism is yet to be discovered in the CETP gene, that will explain the effect on MI associated with TaqIB observed in this study.]. 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:11689220;
    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:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_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" .
}