@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js
> .
@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:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_head
{
this:
np:hasAssertion
dgn-np:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_assertion
;
np:hasProvenance
dgn-np:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_provenance
;
np:hasPublicationInfo
dgn-np:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_assertion
a
np:Assertion
.
dgn-np:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_provenance
a
np:Provenance
.
dgn-np:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_assertion
{
miriam-gene:149233
a
ncit:C16612
.
lld:C0677607
a
ncit:C7057
.
dgn-gda:DGNeb5d021420bd79ef941796b02325922d
sio:SIO_000628
miriam-gene:149233
,
lld:C0677607
;
a
sio:SIO_001121
.
}
dgn-np:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_provenance
{
dgn-np:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_assertion
dcterms:description
"[To determine whether variants in the IL-23R gene are associated with AITDs in Japanese, 464 Japanese AITD patients (290 with GD, 174 with HT) and 179 matched Japanese control subjects were genotyped for four SNPs spanning the IL-23R gene.]. 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:19021011
;
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:NP584088.RAoJDE7Stxw4kQR_0n02DKQZWe8aO_4RBkH_hMT7As2Js130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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" .
}