@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y
> .
@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:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_head
{
this:
np:hasAssertion
dgn-np:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_assertion
;
np:hasProvenance
dgn-np:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_assertion
a
np:Assertion
.
dgn-np:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_provenance
a
np:Provenance
.
dgn-np:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_assertion
{
miriam-gene:5743
a
ncit:C16612
.
lld:C0036572
a
ncit:C7057
.
dgn-gda:DGNcf4db53a74e4f7938eb9b0a39cb39872
sio:SIO_000628
miriam-gene:5743
,
lld:C0036572
;
a
sio:SIO_001121
.
}
dgn-np:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_provenance
{
dgn-np:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_assertion
dct:description
"[The results suggested that brain COX-2 mRNA levels were markedly increased in the hippocampal neurons and the concentration of PGE2 was elevated significantly, and that the incidence of AD and seizure behavior induction and the total AD duration were significantly decreased under conditions of COX-2 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:14518562
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP27800.RAtlVFRIywMUIhLdLSD2m1RvD18oRYh17PH8tcomDNi1Y130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:11+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" .
}