@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs
> .
@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:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_head
{
this:
np:hasAssertion
dgn-np:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_assertion
;
np:hasProvenance
dgn-np:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_provenance
;
np:hasPublicationInfo
dgn-np:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_assertion
a
np:Assertion
.
dgn-np:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_provenance
a
np:Provenance
.
dgn-np:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_assertion
{
miriam-gene:836
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN5edadd78f0a8f74d772121042acf840c
sio:SIO_000628
miriam-gene:836
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_provenance
{
dgn-np:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_assertion
dcterms:description
"[Here we show that the chromosome 21 transcription factor Ets2, a gene that is overexpressed in Down syndrome, is expressed in neurons, and that moderate overexpression of Ets2 leads to increased apoptosis of primary neuronal cultures from Ets2 tg mice that involves activation of caspase-3.]. 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:14678752
;
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:NP594624.RA33VCTqAXOrrR70um2ulySS_FMkUqQ3r7viDQ6vPbZCs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:57+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" .
}