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http://rdf.disgenet.org/nanopublications.trig#NP284818.RApUyUGWcW628N9U7j0Cb96Q9gg-Djufppr1mdG9wkNB4
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
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np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
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;
a
np:Nanopublication
.
dgn-np:NP284818.RApUyUGWcW628N9U7j0Cb96Q9gg-Djufppr1mdG9wkNB4130_assertion
a
np:Assertion
.
dgn-np:NP284818.RApUyUGWcW628N9U7j0Cb96Q9gg-Djufppr1mdG9wkNB4130_provenance
a
np:Provenance
.
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a
np:PublicationInfo
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{
miriam-gene:4137
a
ncit:C16612
.
lld:C0038868
a
ncit:C7057
.
dgn-gda:DGN9dc966d7073e80981c8ae77c7ddce4d3
sio:SIO_000628
miriam-gene:4137
,
lld:C0038868
;
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.
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dgn-np:NP284818.RApUyUGWcW628N9U7j0Cb96Q9gg-Djufppr1mdG9wkNB4130_provenance
{
dgn-np:NP284818.RApUyUGWcW628N9U7j0Cb96Q9gg-Djufppr1mdG9wkNB4130_assertion
dcterms:description
"[The aim of the present study is to investigate UPR activation in sporadic tauopathies like progressive supranuclear palsy (PSP) and Pick's disease (PiD), and familial cases with frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) which carry mutations in the gene encoding for tau (MAPT).]. 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:22102449
;
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:NP284818.RApUyUGWcW628N9U7j0Cb96Q9gg-Djufppr1mdG9wkNB4130_publicationInfo
{
this:
dcterms:created
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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
<
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> , <
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http://orcid.org/0000-0002-9383-528X
> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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pav:version
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