@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00> .
@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:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_head {
  this: np:hasAssertion dgn-np:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_assertion ;
    np:hasProvenance dgn-np:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_provenance ;
    np:hasPublicationInfo dgn-np:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_assertion a np:Assertion .
  dgn-np:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_provenance a np:Provenance .
  dgn-np:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_assertion {
  miriam-gene:50943 a ncit:C16612 .
  lld:C3494489 a ncit:C7057 .
  dgn-gda:DGN54edceda463b8e2d91e3856a16845183 sio:SIO_000628 miriam-gene:50943 , lld:C3494489 ;
    a sio:SIO_001121 .
}
dgn-np:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_provenance {
  dgn-np:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_assertion dcterms:description "[During the last years, analysis of Autoimmune Polyendocrinopathy--Candidiasis--Ectodermal Dystrophy (APECED) and Immunodysregulation--Polyendocrinopathy--Enteropathy--X-linked (IPEX), two rare monogenic forms of immunodeficiency associated with autoimmunity, has led to the identification of Auto Immune Regulator (AIRE) and Forkhead Box P3 (FOXP3), essential transcriptional regulators, involved in central tolerance and peripheral immune homeostasis, respectively.]. 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:16682278 ;
    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:NP279168.RA1Gd-0HsiRNVuL8rK_1KV1J4lW78_V98EXL57NUR2A00130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:37+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" .
}