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http://rdf.disgenet.org/nanopublications.trig#NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk
> .
@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:NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk130_head
{
this:
np:hasAssertion
dgn-np:NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk130_assertion
;
np:hasProvenance
dgn-np:NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk130_provenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk130_assertion
a
np:Assertion
.
dgn-np:NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk130_provenance
a
np:Provenance
.
dgn-np:NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk130_publicationInfo
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np:PublicationInfo
.
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dgn-np:NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk130_assertion
{
miriam-gene:2932
a
ncit:C16612
.
lld:C0011570
a
ncit:C7057
.
dgn-gda:DGN27c95e5e422e4dfa74b201adca0680d3
sio:SIO_000628
miriam-gene:2932
,
lld:C0011570
;
a
sio:SIO_001122
.
}
dgn-np:NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk130_provenance
{
dgn-np:NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk130_assertion
dcterms:description
"[The GSK3beta gene may have a role in determining regional GM volume differences of the right hippocampus and bilateral superior temporal gyri. The association between genotype and brain structure was specific to the patients with MDD, suggesting that GSK3beta genotypes might interact with MDD status. We speculate that this is a consequence of regional neocortical, glial, or neuronal growth or survival. In considering core cognitive features of MDD, the association of GSK3beta polymorphisms with structural variation in the temporal lobe and hippocampus is of particular interest in the context of other evidence for structural and functional abnormalities in the hippocampi of patients with MDD.]. 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:19581563
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP74188.RApDvWJm4XZaB462VejrJMSEdpSuhqHk03WDt2-KVxwFk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+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
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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pav:version
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}