@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y> .
@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:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_head {
  this: np:hasAssertion dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_assertion;
    np:hasProvenance dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_provenance;
    np:hasPublicationInfo dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_assertion a np:Assertion .
  
  dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_provenance a np:Provenance .
  
  dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_assertion {
  miriam-gene:3156 a ncit:C16612 .
  
  lld:C0242339 a ncit:C7057 .
  
  dgn-gda:DGNda8e63610a97168a11ea4936f4116855 sio:SIO_000628 miriam-gene:3156, lld:C0242339;
    a sio:SIO_001122 .
}

dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_provenance {
  dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_assertion dcterms:description
      "[We have identified a common LDLR 3-UTR haplotype that is associated with attenuated lipid-lowering response to simvastatin treatment. Response was further reduced in individuals with both LDLR and previously described HMGCR haplotypes. Previously identified racial differences in statin efficacy were partially explained by the greater prevalence of these combined haplotypes in blacks.]. 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:20413733;
    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:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_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" .
}