@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk> .
@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:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_head {
  this: np:hasAssertion dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_assertion ;
    np:hasProvenance dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_provenance ;
    np:hasPublicationInfo dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_assertion a np:Assertion .
  dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_provenance a np:Provenance .
  dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_assertion {
  miriam-gene:1071 a ncit:C16612 .
  lld:C0011860 a ncit:C7057 .
  dgn-gda:DGN600502c0fd60fd2d69db07efc23eb662 sio:SIO_000628 miriam-gene:1071 , lld:C0011860 ;
    a sio:SIO_001122 .
}
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_provenance {
  dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_assertion dcterms:description "[ In conclusion, the B1B1/CC carriers of the CETP polymorphisms have a more atherogenic lipid profile, including low HDL, and they respond better to statin therapy. These results favor the hypothesis that CETP polymorphisms modify the effect of statin treatment and may help to identify patients who will benefit most from statin therapy.]. 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:12663600 ;
    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:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_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" .
}