@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY
> .
@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 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:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_head
{
this:
np:hasAssertion
dgn-np:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_assertion
;
np:hasProvenance
dgn-np:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_provenance
;
np:hasPublicationInfo
dgn-np:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_assertion
a
np:Assertion
.
dgn-np:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_provenance
a
np:Provenance
.
dgn-np:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_assertion
{
miriam-gene:1493
a
ncit:C16612
.
lld:C0018213
a
ncit:C7057
.
dgn-gda:DGN00f541a3677753ef270dc5df1af5b101
sio:SIO_000628
miriam-gene:1493
,
lld:C0018213
;
a
sio:SIO_001122
.
}
dgn-np:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_provenance
{
dgn-np:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_assertion
dct:description
"[The frequency of CTLA-4 +49A>G polymorphism is not different in children and adults with GD compared to the normal control population and does not seem to contribute independently to the severity of the clinical presentation of GD.]. 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:18493148
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}