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http://rdf.disgenet.org/nanopublications.trig#NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_assertion
a
np:Assertion
.
dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_provenance
a
np:Provenance
.
dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:139596
a
ncit:C16612
.
lld:C0270952
a
ncit:C7057
.
dgn-gda:DGN05065182a137bf15338a870afb4b8a65
sio:SIO_000628
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,
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;
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.
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dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_provenance
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dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_assertion
dcterms:description
"[Further analysis of the cellular and molecular mechanisms by which UPP and molecular chaperones influence the degradation of misfolded proteins could provide novel concepts and targets for the treatment and understanding of the pathogenesis of OPMD and neurodegenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:12944420
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
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dgn-void:befree-20140225
pav:importedOn
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xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
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rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
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dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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pav:authoredBy
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> , <
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> , <
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pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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