@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" .
}