@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg> .
@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 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:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_head {
  this: np:hasAssertion dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_assertion;
    np:hasProvenance dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_provenance;
    np:hasPublicationInfo dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_assertion a np:Assertion .
  
  dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_provenance a np:Provenance .
  
  dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN92b001d1252c5819583bee1dc7ac84b4 sio:SIO_000628 miriam-gene:3949, lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_provenance {
  dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_assertion dct: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:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_publicationInfo {
  this: dct:created "2014-10-02T12:32:34+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}