@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778036.RAu0jUQxnhrpz0YPN9nf2u767GJEa2lrqQbFpfhHrBc2E
> .
@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:NP778036.RAu0jUQxnhrpz0YPN9nf2u767GJEa2lrqQbFpfhHrBc2E130_head
{
this:
np:hasAssertion
dgn-np:NP778036.RAu0jUQxnhrpz0YPN9nf2u767GJEa2lrqQbFpfhHrBc2E130_assertion
;
np:hasProvenance
dgn-np:NP778036.RAu0jUQxnhrpz0YPN9nf2u767GJEa2lrqQbFpfhHrBc2E130_provenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP778036.RAu0jUQxnhrpz0YPN9nf2u767GJEa2lrqQbFpfhHrBc2E130_provenance
a
np:Provenance
.
dgn-np:NP778036.RAu0jUQxnhrpz0YPN9nf2u767GJEa2lrqQbFpfhHrBc2E130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:50943
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN70ca86e38c3af20c45b94a76ccb3e1fe
sio:SIO_000628
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,
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;
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.
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dgn-np:NP778036.RAu0jUQxnhrpz0YPN9nf2u767GJEa2lrqQbFpfhHrBc2E130_provenance
{
dgn-np:NP778036.RAu0jUQxnhrpz0YPN9nf2u767GJEa2lrqQbFpfhHrBc2E130_assertion
dcterms:description
"[The aim of this study was to assess the possible association of the functional (GT)(n) microsatellite polymorphism in the FOXP3 gene with predisposition to several autoimmune diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), ulcerative colitis (UC), Crohn's disease, and celiac disease.]. 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:16216670
;
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 .
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dgn-np:NP778036.RAu0jUQxnhrpz0YPN9nf2u767GJEa2lrqQbFpfhHrBc2E130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> , <
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> , <
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> , <
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> ;
pav:createdBy
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> ;
pav:version
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dgn-void:disgenetrdf
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}