@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk
> .
@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:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_head
{
this:
np:hasAssertion
dgn-np:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_assertion
;
np:hasProvenance
dgn-np:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_provenance
;
np:hasPublicationInfo
dgn-np:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_assertion
a
np:Assertion
.
dgn-np:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_provenance
a
np:Provenance
.
dgn-np:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_assertion
{
miriam-gene:1786
a
ncit:C16612
.
lld:C0033975
a
ncit:C7057
.
dgn-gda:DGNd660721349e578574ebf96db6fd00287
sio:SIO_000628
miriam-gene:1786
,
lld:C0033975
;
a
sio:SIO_001121
.
}
dgn-np:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_provenance
{
dgn-np:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_assertion
dcterms:description
"[To unravel how this pathological DNMT1 overexpression induces GABAergic neuronal dysfunction in SZ and in other psychoses, we report on how alterations in methylation modify the expression of susceptible vulnerability genes such as reelin or GAD67 in these neurons.]. 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:17965595
;
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:NP520625.RAdwC6gwRTX2L-L8BVm1TWvFNaLYKFtuT72RE7dN0UHnk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}