@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg> .
@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:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_head {
  this: np:hasAssertion dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_assertion;
    np:hasProvenance dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_provenance;
    np:hasPublicationInfo dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_assertion a np:Assertion .
  
  dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_provenance a np:Provenance .
  
  dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_assertion {
  miriam-gene:7350 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGNbdc1befefd5ce549e0c79ee4581eb363 sio:SIO_000628 miriam-gene:7350, lld:C0027051;
    a sio:SIO_001121 .
}

dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_provenance {
  dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_assertion dcterms:description
      "[Participants from the Utrecht Cardiovascular Pharmacogenetics (UCP) studies were enrolled from a population-based registry of pharmacy records linked to hospital discharge records (PHARMO) to investigate tagging SNPs within candidate genes involved in the cholesterol lowering pathway for modification of the effectiveness of statins in reducing the risk of myocardial infarction (MI).]. 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:21741043;
    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:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:56+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" .
}