@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo
> .
@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:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_head
{
this:
np:hasAssertion
dgn-np:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_assertion
;
np:hasProvenance
dgn-np:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_provenance
;
np:hasPublicationInfo
dgn-np:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_assertion
a
np:Assertion
.
dgn-np:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_provenance
a
np:Provenance
.
dgn-np:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_assertion
{
miriam-gene:50943
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGN35e8f41ed38889d2d541e01611c6bdea
sio:SIO_000628
miriam-gene:50943
,
lld:C0009324
;
a
sio:SIO_001121
.
}
dgn-np:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_provenance
{
dgn-np:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_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 .
}
dgn-np:NP885365.RAsiUUHXh0KCkvLOcpjqh0TjmV26G5scLvjigzg4DEHwo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}