@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk
> .
@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:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_head
{
this:
np:hasAssertion
dgn-np:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_assertion
;
np:hasProvenance
dgn-np:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_provenance
;
np:hasPublicationInfo
dgn-np:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_assertion
a
np:Assertion
.
dgn-np:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_provenance
a
np:Provenance
.
dgn-np:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_assertion
{
miriam-gene:57030
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGN89ba57bdb7c24602809d7bba476fe4ca
sio:SIO_000628
miriam-gene:57030
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_provenance
{
dgn-np:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_assertion
dcterms:description
"[We found decreased VGLUT1 mRNA expression in both MDD and BD in the entorhinal cortex (ERC), decreased VGLUT2 mRNA expression in MDD in the middle temporal gyrus, and increased VGLUT2 mRNA expression in SCZ in the inferior temporal gyrus (ITG).]. 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:19839996
;
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:NP525749.RARCd9iaF1Pfci5O8MTZV4_FiaAdkftgk6XgBuNZOxHhk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}