@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI
> .
@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 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:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_head
{
this:
np:hasAssertion
dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_assertion
;
np:hasProvenance
dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_provenance
;
np:hasPublicationInfo
dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_assertion
a
np:Assertion
.
dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_provenance
a
np:Provenance
.
dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_assertion
{
miriam-gene:7417
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNb1c1f970d2923b25aa127619e895d108
sio:SIO_000628
miriam-gene:7417
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_provenance
{
dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_assertion
dc:description
"[These findings indicate that the increase of VDAC1 and the decrease of VDAC2 play an important role during the process and provide new molecular evidence in understanding mechanism of refractory epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:17893921
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP33512.RAC3oYeLaxsa-STtU5dS0QKOm0sURvnmWo5bNaE4eE7lI130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:14+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}