@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_head {
  this: np:hasAssertion dgn-np:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_assertion;
    np:hasProvenance dgn-np:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_provenance;
    np:hasPublicationInfo dgn-np:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_assertion a np:Assertion .
  
  dgn-np:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_provenance a np:Provenance .
  
  dgn-np:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_assertion {
  miriam-gene:1557 a ncit:C16612 .
  
  lld:C0403447 a ncit:C7057 .
  
  dgn-gda:DGNadc659b64b7a76cf33f48f3130e4fba8 sio:SIO_000628 miriam-gene:1557, lld:C0403447;
    a sio:SIO_001121 .
}

dgn-np:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_provenance {
  dgn-np:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_assertion dcterms:description
      "[We analyzed the incidence of CYP2C19 polymorphism and its association with the development of CAD in the absence of diabetes, dyslipidemia, and chronic kidney disease to minimize the influence of conventional coronary risk factors.]. 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:25264752;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1224489.RAiKS3q-qWuq8jklW2cNFnFwo5EMfO2yW7tty5s5AgkpM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:01+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}