@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0> .
@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:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_head {
  this: np:hasAssertion dgn-np:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_assertion;
    np:hasProvenance dgn-np:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_provenance;
    np:hasPublicationInfo dgn-np:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_assertion a np:Assertion .
  
  dgn-np:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_provenance a np:Provenance .
  
  dgn-np:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_assertion {
  miriam-gene:3990 a ncit:C16612 .
  
  lld:C0020473 a ncit:C7057 .
  
  dgn-gda:DGN7fab755d03ae8c0240beb9f65107e579 sio:SIO_000628 miriam-gene:3990, lld:C0020473;
    a sio:SIO_001122 .
}

dgn-np:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_provenance {
  dgn-np:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_assertion dcterms:description
      "[An intronic single nucleotide polymorphism in ABCA1 and the APOE epsilon3 allele are associated with reduced LDLc lowering by statins and identify individuals who may be resistant to maximal LDLc lowering by statins.]. 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:20031551;
    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:NP84593.RAr2-taVjvZ2MR61wdj586eeOMqHai_Wcw9UEXl_PE2S0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:41+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" .
}