@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4
> .
@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:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_head
{
this:
np:hasAssertion
dgn-np:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_assertion
;
np:hasProvenance
dgn-np:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_provenance
;
np:hasPublicationInfo
dgn-np:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_assertion
a
np:Assertion
.
dgn-np:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_provenance
a
np:Provenance
.
dgn-np:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C1868682
a
ncit:C7057
.
dgn-gda:DGN8626a4f3c02e09ed002d2bda0e9873ae
sio:SIO_000628
miriam-gene:351
,
lld:C1868682
;
a
sio:SIO_001121
.
}
dgn-np:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_provenance
{
dgn-np:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_assertion
dcterms:description
"[Our data indicate that neuronal overexpression of APPsw causes a dynamic change in neuronal expression and activation of multiple PKC isoforms known to be regulators of proteolytic amyloid precursor protein (APP) processing (PKC alpha) and of neuronal survival (PKC lambda and PKC zeta).]. 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:11168531
;
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:NP815253.RALlxLNJATJNV6n6fc4eT-WU03XF_9HMhbY0KhU_s3Kx4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:19+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" .
}