@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew> .
@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:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_head {
  this: np:hasAssertion dgn-np:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_assertion;
    np:hasProvenance dgn-np:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_provenance;
    np:hasPublicationInfo dgn-np:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_assertion a np:Assertion .
  
  dgn-np:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_provenance a np:Provenance .
  
  dgn-np:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_assertion {
  miriam-gene:3663 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN956ad2e5884429196bea570c8082bd8e sio:SIO_000628 miriam-gene:3663, lld:C0024141;
    a sio:SIO_001122 .
}

dgn-np:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_provenance {
  dgn-np:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_assertion dct:description
      "[The aim of this study was to determine whether the IRF5 SLE risk haplotype mediates the risk of SLE by predisposing patients to the development of high levels of serum IFNalpha activity.]. 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:18668568;
    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:NP71729.RAYzANTWAq6vRSxDASsjSb2RJ1SH1G6geUE6wtXjhmoew130_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" .
}