@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP445245.RAtlLFT7RwKEgHT-BLi5iVnj037FtLq3ghcLE-jZ_O4Ps
> .
@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#
> .
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{
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np:hasProvenance
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a
np:Nanopublication
.
dgn-np:NP445245.RAtlLFT7RwKEgHT-BLi5iVnj037FtLq3ghcLE-jZ_O4Ps130_assertion
a
np:Assertion
.
dgn-np:NP445245.RAtlLFT7RwKEgHT-BLi5iVnj037FtLq3ghcLE-jZ_O4Ps130_provenance
a
np:Provenance
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{
miriam-gene:3630
a
ncit:C16612
.
lld:C0178468
a
ncit:C7057
.
dgn-gda:DGNcd74bebed35eeb00b65e1b3445ba21d4
sio:SIO_000628
miriam-gene:3630
,
lld:C0178468
;
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.
}
dgn-np:NP445245.RAtlLFT7RwKEgHT-BLi5iVnj037FtLq3ghcLE-jZ_O4Ps130_provenance
{
dgn-np:NP445245.RAtlLFT7RwKEgHT-BLi5iVnj037FtLq3ghcLE-jZ_O4Ps130_assertion
dcterms:description
"[Furthermore, a joint analysis, with the INS and CTLA4 SNPs, revealed that CTLA4 rs3087243, ERBB3 rs2292399, and CLEC16A rs2903692, but not INS rs689, were significant risk factors for the cooccurrence of AITD in Japanese T1D.]. 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:18940880
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
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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:NP445245.RAtlLFT7RwKEgHT-BLi5iVnj037FtLq3ghcLE-jZ_O4Ps130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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> ;
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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