@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0> .
@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:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_head {
  this: np:hasAssertion dgn-np:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_assertion;
    np:hasProvenance dgn-np:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_provenance;
    np:hasPublicationInfo dgn-np:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_assertion a np:Assertion .
  
  dgn-np:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_provenance a np:Provenance .
  
  dgn-np:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_assertion {
  miriam-gene:221458 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN98a12b747d43351b98ae0a6fcca706cd sio:SIO_000628 miriam-gene:221458, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_provenance {
  dgn-np:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_assertion dcterms:description
      "[Our data indicate that the assessment of KIF6 rs20455 and TAS2R50 rs1376251 genotypes are not useful for predicting statin induced cardiovascular risk reduction in men, but do predict CHD risk reduction in women in this elderly population.]. 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:22192511;
    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:NP479167.RAhlXjEfAp26IyD767MKH_AaTFxY1MeiB3oy1ucdEpfY0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:47+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" .
}