@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM> .
@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:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_head {
  this: np:hasAssertion dgn-np:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_assertion;
    np:hasProvenance dgn-np:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_provenance;
    np:hasPublicationInfo dgn-np:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_assertion a np:Assertion .
  
  dgn-np:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_provenance a np:Provenance .
  
  dgn-np:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_assertion {
  miriam-gene:6775 a ncit:C16612 .
  
  lld:C1527336 a ncit:C7057 .
  
  dgn-gda:DGN795080549fcbcd83a2e712c687a592ba sio:SIO_000628 miriam-gene:6775, lld:C1527336;
    a sio:SIO_001121 .
}

dgn-np:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_provenance {
  dgn-np:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_assertion dcterms:description
      "[STAT4, a transcription factor transmitting signals induced by several key cytokines, has recently been identified as a genetic risk factor for rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and Sjögren's disease (SD), thus indicating that multiple autoimmune diseases may share common biochemical pathways that lead to immune deregulation.]. 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:18703106;
    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:NP661035.RAY_Bm8X2-H_PcXeoa2BRjmW9_gqa1zIApf7TUa3ZnCkM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}