@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ
> .
@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:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_head
{
this:
np:hasAssertion
dgn-np:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_assertion
;
np:hasProvenance
dgn-np:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_assertion
a
np:Assertion
.
dgn-np:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_provenance
a
np:Provenance
.
dgn-np:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_assertion
{
miriam-gene:2902
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGN7c4988f3c24b7d8f3f83f5f65e2b7f76
sio:SIO_000628
miriam-gene:2902
,
lld:C0005586
;
a
sio:SIO_001121
.
}
dgn-np:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_provenance
{
dgn-np:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_assertion
dcterms:description
"[In the perirhinal cortex we detected decreased expression of GluR5 in all three diagnoses, of GluR1, GluR3, NR2B in both BD and MDD, and decreased NR1 and NR2A in BD and MDD, respectively.]. 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:17299517
;
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:NP274825.RAIfjXPTWZXiH4w9W72kl5iO7RAEtWETJzyEPIaenqizQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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" .
}