@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo> .
@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:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_head {
  this: np:hasAssertion dgn-np:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_assertion;
    np:hasProvenance dgn-np:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_provenance;
    np:hasPublicationInfo dgn-np:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_assertion a np:Assertion .
  
  dgn-np:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_provenance a np:Provenance .
  
  dgn-np:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_assertion {
  miriam-gene:3240 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGNbc8b9fafd477f249a73e027125469989 sio:SIO_000628 miriam-gene:3240, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_provenance {
  dgn-np:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_assertion dcterms:description
      "[The study thus indicated that genetic variation of APOB, LPL, CETP, and lecithin cholesterol acyl transferase (which is linked to HPA and CETP) may play an important role in the regulation of lipoprotein metabolism and could contribute to the risk of coronary artery disease.]. 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:8279486;
    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:NP661654.RANsODl8s5U6xIlo-Wu7nvnz7yr5abZ8Wyerq_OGjygdo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}