@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4> .
@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:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_head {
  this: np:hasAssertion dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_assertion;
    np:hasProvenance dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_provenance;
    np:hasPublicationInfo dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_assertion a np:Assertion .
  
  dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_provenance a np:Provenance .
  
  dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_assertion {
  miriam-gene:3663 a ncit:C16612 .
  
  lld:C0004364 a ncit:C7057 .
  
  dgn-gda:DGNa15aa3a6bd0f450d0e7a11a9f641f53a sio:SIO_000628 miriam-gene:3663, lld:C0004364;
    a sio:SIO_001121 .
}

dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_provenance {
  dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_assertion dcterms:description
      "[Functional genetic variants associated with increased IRF5 expression of specific isoforms are associated with systemic lupus erythematosus (SLE) and it is possible that they may also predispose to other autoimmune disorders.]. 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:17557928;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:41+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" .
}