@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck> .
@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:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_head {
  this: np:hasAssertion dgn-np:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_assertion;
    np:hasProvenance dgn-np:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_provenance;
    np:hasPublicationInfo dgn-np:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_assertion a np:Assertion .
  
  dgn-np:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_provenance a np:Provenance .
  
  dgn-np:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_assertion {
  miriam-gene:1071 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGNe91f78e276209b82b1f31f0a4b856473 sio:SIO_000628 miriam-gene:1071, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_provenance {
  dgn-np:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_assertion dcterms:description
      "[To determine the frequency of CETP TaqIB variants and to examine the possible association between CETP TaqIB polymorphism with CAD and T2DM, we studied 207 unrelated patients with CAD, 101 patients with T2DM, and 92 controls.]. 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:21689002;
    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:NP430662.RASaiVUGjeSPKp_lGLo2YxGGcAGYc7e1FIb39N3bohWck130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:15+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" .
}