@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q> .
@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:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_head {
  this: np:hasAssertion dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_assertion;
    np:hasProvenance dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_provenance;
    np:hasPublicationInfo dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_assertion a np:Assertion .
  
  dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_provenance a np:Provenance .
  
  dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_assertion {
  miriam-gene:335 a ncit:C16612 .
  
  lld:C0020473 a ncit:C7057 .
  
  dgn-gda:DGN9bff01dc9c22c3edb8908035b711304a sio:SIO_000628 miriam-gene:335, lld:C0020473;
    a sio:SIO_001122 .
}

dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_provenance {
  dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_assertion dct: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:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+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" .
}