@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog
> .
@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:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_head
{
this:
np:hasAssertion
dgn-np:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_assertion
;
np:hasProvenance
dgn-np:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_provenance
;
np:hasPublicationInfo
dgn-np:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_assertion
a
np:Assertion
.
dgn-np:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_provenance
a
np:Provenance
.
dgn-np:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_assertion
{
miriam-gene:25814
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGN3d7fe9218892cfe47b8991bd5b8dc344
sio:SIO_000628
miriam-gene:25814
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_provenance
{
dgn-np:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_assertion
dcterms:description
"[Reduced expression of E46L in primary neuronal cultures from cerebellum and cortex by small interfering RNAs (siRNAs) caused increased apoptosis, raising the possibility that reduced expression of E46L might also play an important role in SCA10 pathogenesis.]. 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:15895557
;
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:NP931696.RA3QPqH4bWkiy2iok59NxmG-20E6nnk7Vzmw6jXrOwWog130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}