@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM> .
@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:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_head {
  this: np:hasAssertion dgn-np:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_assertion;
    np:hasProvenance dgn-np:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_provenance;
    np:hasPublicationInfo dgn-np:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_assertion a np:Assertion .
  
  dgn-np:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_provenance a np:Provenance .
  
  dgn-np:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_assertion {
  miriam-gene:1071 a ncit:C16612 .
  
  lld:C3149462 a ncit:C7057 .
  
  dgn-gda:DGN509d66283fe2c9fe0aadc2f81068e94f sio:SIO_000628 miriam-gene:1071, lld:C3149462;
    a sio:SIO_001121 .
}

dgn-np:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_provenance {
  dgn-np:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_assertion dcterms:description
      "[To further clarify the characteristics of marked HALP in patients with ACD, we compared the plasma lipids, lipoproteins, CETP, and HTGL activities between heterozygotes for CETP deficiency who were with and without ACD.]. 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:7583564;
    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:NP207909.RAKPcsZN7EvFiokLruvIcWe2fvdax3DB_WYiSsYEoWsYM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:54+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" .
}