@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI> .
@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:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_head {
  this: np:hasAssertion dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_assertion;
    np:hasProvenance dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_provenance;
    np:hasPublicationInfo dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_assertion a np:Assertion .
  
  dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_provenance a np:Provenance .
  
  dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_assertion {
  miriam-gene:4023 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN357ee6eaa4eefb12ccd570e7f8be551a sio:SIO_000628 miriam-gene:4023, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_provenance {
  dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_assertion dcterms:description
      "[our results are consistent with the previously reported role of CETP and LPL genetic variants in cardiovascular risk and the possible modulation of the association between hypertension and carotid IMT by APOCIII Sst-1 variant.]. 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:16430904;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:04+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" .
}