@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI> .
@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:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_head {
  this: np:hasAssertion dgn-np:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_assertion;
    np:hasProvenance dgn-np:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_provenance;
    np:hasPublicationInfo dgn-np:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_assertion a np:Assertion .
  
  dgn-np:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_provenance a np:Provenance .
  
  dgn-np:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0020473 a ncit:C7057 .
  
  dgn-gda:DGN8be25c93d1bb29cf5807340383372502 sio:SIO_000628 miriam-gene:3949, lld:C0020473;
    a sio:SIO_001122 .
}

dgn-np:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_provenance {
  dgn-np:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_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:NP55457.RAloeGbzr7GfI8MKzszo72rQULeCPkLMTNQdPnmb4LZSI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}