@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU
> .
@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:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_head
{
this:
np:hasAssertion
dgn-np:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_assertion
;
np:hasProvenance
dgn-np:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_provenance
;
np:hasPublicationInfo
dgn-np:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_assertion
a
np:Assertion
.
dgn-np:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_provenance
a
np:Provenance
.
dgn-np:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_assertion
{
miriam-gene:2902
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGN3271560cfc0d06ccd1668b1f1c757643
sio:SIO_000628
miriam-gene:2902
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_provenance
{
dgn-np:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_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:NP503370.RALM8mQMdlkSHlqAxf30j3bCnqxmnXBeg73yQyfjxCutU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}