@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM
> .
@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:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_head
{
this:
np:hasAssertion
dgn-np:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_assertion
;
np:hasProvenance
dgn-np:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_provenance
;
np:hasPublicationInfo
dgn-np:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_assertion
a
np:Assertion
.
dgn-np:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_provenance
a
np:Provenance
.
dgn-np:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_assertion
{
miriam-gene:2670
a
ncit:C16612
.
lld:C0007786
a
ncit:C7057
.
dgn-gda:DGNe980fce9a1bed3a5de5fbf3a18522b73
sio:SIO_000628
miriam-gene:2670
,
lld:C0007786
;
a
sio:SIO_001121
.
}
dgn-np:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_provenance
{
dgn-np:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_assertion
dcterms:description
"[Modulation by hMSCs in our in vivo and in vitro study shows they decrease markers of microglial activation (lower ED1 and Iba) and astrogliosis (lower GFAP) following transplantation in an ouabain-induced brain ischemia rat model and in organotypic hippocampal cultures.]. 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:23466243
;
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:NP763518.RAIojeROg5Q7iSkyrN8RN-qw5iB2EPb8k12QGDT2MXmqM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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" .
}