@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM> .
@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:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_head {
  this: np:hasAssertion dgn-np:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_assertion;
    np:hasProvenance dgn-np:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_provenance;
    np:hasPublicationInfo dgn-np:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_assertion a np:Assertion .
  
  dgn-np:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_provenance a np:Provenance .
  
  dgn-np:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_assertion {
  miriam-gene:4179 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN69ad7fc00ecaaf67ae70b4b504d53e67 sio:SIO_000628 miriam-gene:4179, lld:C0024141;
    a sio:SIO_001122 .
}

dgn-np:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_provenance {
  dgn-np:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_assertion dcterms:description
      "[These results indicate an association between the presence of G at position minus sign2518 in the MCP-1 promoter region and the presence of cutaneous vasculitis among patients with SLE. This polymorphism does not seem to influence the susceptibility to SLE nor the appearance of lupus nephritis. Further studies are necessary in order to elucidate the role of this polymorphism in the pathogenesis of other inflammatory autoimmune diseases.]. 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:11844145;
    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:NP54832.RAe4iSVrseiocBhK7dMehPtq6BBfZpZWuh0ClDbmSjIjM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}