@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs> .
@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:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_head {
  this: np:hasAssertion dgn-np:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_assertion;
    np:hasProvenance dgn-np:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_provenance;
    np:hasPublicationInfo dgn-np:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_assertion a np:Assertion .
  
  dgn-np:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_provenance a np:Provenance .
  
  dgn-np:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_assertion {
  miriam-gene:341 a ncit:C16612 .
  
  lld:C0021368 a ncit:C7057 .
  
  dgn-gda:DGNab051cf943ca1b8456f12b836384add5 sio:SIO_000628 miriam-gene:341, lld:C0021368;
    a sio:SIO_001122 .
}

dgn-np:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_provenance {
  dgn-np:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_assertion dcterms:description
      "[Using combined GWA analysis from three clinical trials involving nearly 4,000 individuals treated with simvastatin, pravastatin, or atorvastatin, we have identified SNPs that may be associated with variation in the magnitude of statin-mediated reduction in total and LDL-cholesterol, including one in the CLMN gene for which statistical evidence for association exceeds conventional levels of genome-wide significance.]. 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:20339536;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP85673.RATgiOevWrmQ9aohjGz4_-BnEjNOYidKi0vEsOQpjkLTs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+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" .
}