@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA> .
@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:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_head {
  this: np:hasAssertion dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_assertion;
    np:hasProvenance dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_provenance;
    np:hasPublicationInfo dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_assertion a np:Assertion .
  
  dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_provenance a np:Provenance .
  
  dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_assertion {
  miriam-gene:1071 a ncit:C16612 .
  
  lld:C0577631 a ncit:C7057 .
  
  dgn-gda:DGNc80b2cb17cd56bcba151e04de1c0e849 sio:SIO_000628 miriam-gene:1071, lld:C0577631;
    a sio:SIO_001121 .
}

dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_provenance {
  dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_assertion dcterms:description
      "[CETP and LIPC polymorphisms influence the respective hepatic transcript levels, demonstrate interactions on HDL cholesterol and suggest that imbalances between CETP and LIPC activities may modulate the risk of carotid atherosclerosis.]. 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:21371711;
    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:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}