@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_assertion
;
np:hasProvenance
dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_provenance
;
np:hasPublicationInfo
dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_assertion
a
np:Assertion
.
dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_provenance
a
np:Provenance
.
dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_assertion
{
miriam-gene:1786
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGN110ace59a51df12e3167c1a06243d387
sio:SIO_000628
miriam-gene:1786
,
lld:C0525045
;
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sio:SIO_001121
.
}
dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_provenance
{
dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_assertion
dcterms:description
"[Thus, our data suggest that the altered expression of DNMTs is state dependent and that the aberrant epigenetic gene regulations caused by the altered expression of DNMT1 and DNMT3B may be associated with the pathophysiology of mood disorders.]. 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:21592522
;
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 .
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dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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
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