@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q
> .
@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:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_head
{
this:
np:hasAssertion
dgn-np:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_assertion
;
np:hasProvenance
dgn-np:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_assertion
a
np:Assertion
.
dgn-np:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_provenance
a
np:Provenance
.
dgn-np:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C2921627
a
ncit:C7057
.
dgn-gda:DGNd853cc1bd5dbc62079a21ba333ca8f15
sio:SIO_000628
miriam-gene:4397
,
lld:C2921627
;
a
sio:SIO_001121
.
}
dgn-np:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_provenance
{
dgn-np:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_assertion
dcterms:description
"[We previously reported that low expression of the antiproliferative gene TOB1 in CD4⁺ T cells of individuals presenting with an initial central nervous system (CNS) demyelinating event (a clinically isolated syndrome), correlated with high risk for progression to MS. We report that experimental autoimmune encephalomyelitis (EAE) in Tob1⁻/ ⁻ mice was associated with augmented CNS inflammation, increased infiltrating CD4⁺ and CD8⁺ T cell counts, and increased myelin-reactive Th1 and Th17 cells, with reduced numbers of regulatory T cells.]. 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:23797093
;
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:NP652629.RAcBZN197jTANiLa11REur7Zh-dcB_XfVa5FZkJIAkm_Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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" .
}