@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU> .
@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:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_head {
   this: np:hasAssertion dgn-np:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_assertion ;
    np:hasProvenance dgn-np:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_provenance ;
    np:hasPublicationInfo dgn-np:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_assertion a np:Assertion .
  dgn-np:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_provenance a np:Provenance .
  dgn-np:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_assertion {
   miriam-gene:116519 a ncit:C16612 .
  lld:C0010054 a ncit:C7057 .
  dgn-gda:DGN81fdcac7e4640a2a07ec4634dc88c9b9 sio:SIO_000628 miriam-gene:116519 , lld:C0010054 ;
    a sio:SIO_001122 .
}
dgn-np:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_provenance {
   dgn-np:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_assertion dct:description "[There was no effect of genotype on the response of these parameters to gemfibrozil treatment. These results shed new light on the role of APOA5 variants in TG metabolism and CHD risk.]. 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:14729863 ;
    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:NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_publicationInfo {
   this: dct:created "2014-10-02T12:32:22+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" .
}