@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP620910.RAKRcYTfl78-d715HWZkS81tPNJXG12TU8Dn8wvpwwk54
> .
@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:NP620910.RAKRcYTfl78-d715HWZkS81tPNJXG12TU8Dn8wvpwwk54130_assertion
;
np:hasProvenance
dgn-np:NP620910.RAKRcYTfl78-d715HWZkS81tPNJXG12TU8Dn8wvpwwk54130_provenance
;
np:hasPublicationInfo
dgn-np:NP620910.RAKRcYTfl78-d715HWZkS81tPNJXG12TU8Dn8wvpwwk54130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP620910.RAKRcYTfl78-d715HWZkS81tPNJXG12TU8Dn8wvpwwk54130_assertion
a
np:Assertion
.
dgn-np:NP620910.RAKRcYTfl78-d715HWZkS81tPNJXG12TU8Dn8wvpwwk54130_provenance
a
np:Provenance
.
dgn-np:NP620910.RAKRcYTfl78-d715HWZkS81tPNJXG12TU8Dn8wvpwwk54130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:8851
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN75bdbcda054637849ab6564b0dd7cfa6
sio:SIO_000628
miriam-gene:8851
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP620910.RAKRcYTfl78-d715HWZkS81tPNJXG12TU8Dn8wvpwwk54130_provenance
{
dgn-np:NP620910.RAKRcYTfl78-d715HWZkS81tPNJXG12TU8Dn8wvpwwk54130_assertion
dcterms:description
"[These results indicate a novel role for p25 in the secretory pathway and suggest that elevated levels of p25 and BACE1 in AD brains may contribute to altered neurotransmitter pathology of AD through enhancing spontaneous basal secretion.]. 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:20033852
;
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:NP620910.RAKRcYTfl78-d715HWZkS81tPNJXG12TU8Dn8wvpwwk54130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:15+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
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"v2.1.0" .
}