@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M> .
@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:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_head {
  this: np:hasAssertion dgn-np:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_assertion ;
    np:hasProvenance dgn-np:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_provenance ;
    np:hasPublicationInfo dgn-np:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_assertion a np:Assertion .
  dgn-np:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_provenance a np:Provenance .
  dgn-np:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_assertion {
  miriam-gene:3156 a ncit:C16612 .
  lld:C0007222 a ncit:C7057 .
  dgn-gda:DGN68f2c8241e3513879d102f37762bf5e8 sio:SIO_000628 miriam-gene:3156 , lld:C0007222 ;
    a sio:SIO_001122 .
}
dgn-np:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_provenance {
  dgn-np:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_assertion dcterms:description "[Our purpose was to evaluate associations of single nucleotide polymorphisms (SNPs) at the low density lipoprotein (LDL) receptor (LDLR C44857T, minor allele frequency (MAF) 0.26, and A44964G, MAF 0.25, both in the untranslated region) and HMG-CoA reductase (HMGCR i18 T>G, MAF 0.019) gene loci with baseline lipid values, statin-induced LDL-cholesterol (C) lowering response, and incident coronary heart disease (CHD) and cardiovascular disease (CVD) on trial.]. 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:18261733 ;
    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:NP73383.RA25NXS9aMsvtBNjmalWIUG5fCdE3IS34RahVjKkOkE_M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:35+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" .
}