@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY> .
@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:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_head {
  this: np:hasAssertion dgn-np:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_assertion;
    np:hasProvenance dgn-np:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_provenance;
    np:hasPublicationInfo dgn-np:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_assertion a np:Assertion .
  
  dgn-np:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_provenance a np:Provenance .
  
  dgn-np:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_assertion {
  miriam-gene:1917 a ncit:C16612 .
  
  lld:C0242339 a ncit:C7057 .
  
  dgn-gda:DGNab0237143f3d285f751380310239b60f sio:SIO_000628 miriam-gene:1917, lld:C0242339;
    a sio:SIO_001121 .
}

dgn-np:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_provenance {
  dgn-np:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_assertion dcterms:description
      "[Single nucleotide polymorphisms (SNPs) and haplotypes in the CETP gene were determined in 98 patients with untreated dyslipidemias and analyzed for associations with plasma CETP and plasma lipids before and during statin treatment.]. 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:14583798;
    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:NP857949.RAQsoRtnGQmHCXCNW5rcLaYvJ50YfecsJdxv7VIy1qKgY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:44+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}