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http://rdf.disgenet.org/nanopublications.trig#NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_publicationInfo
;
a
np:Nanopublication
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dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_assertion
a
np:Assertion
.
dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_provenance
a
np:Provenance
.
dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_publicationInfo
a
np:PublicationInfo
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dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_assertion
{
miriam-gene:50943
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN5633ae21b8fd6570eb45f280216ee0eb
sio:SIO_000628
miriam-gene:50943
,
lld:C0003873
;
a
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.
}
dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_provenance
{
dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_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:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
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