@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE
> .
@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:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_head
{
this:
np:hasAssertion
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_assertion
;
np:hasProvenance
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_provenance
;
np:hasPublicationInfo
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_assertion
a
np:Assertion
.
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_provenance
a
np:Provenance
.
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_assertion
{
miriam-gene:1493
a
ncit:C16612
.
lld:C0004943
a
ncit:C7057
.
dgn-gda:DGN6c9a56ab9452d598a0c5949b21a87774
sio:SIO_000628
miriam-gene:1493
,
lld:C0004943
;
a
sio:SIO_001121
.
}
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_provenance
{
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_assertion
dcterms:description
"[Although our understanding of the role of the CTLA4 gene and its protein product in BD is incomplete, these results suggest that single nucleotide polymorphisms of the promoter and exon regions in the CTLA4 gene are candidates that predispose to BD and that sCTLA4 may be related to the immunological abnormalities and disease expressions associated with BD.]. 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:19563524
;
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:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}