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> .
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> .
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http://www.w3.org/2001/XMLSchema#
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http://semanticscience.org/resource/
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@prefix ncit: <
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http://linkedlifedata.com/resource/umls/id/
> .
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http://identifiers.org/ncbigene/
> .
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http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
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http://www.w3.org/ns/prov#
> .
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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#
> .
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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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np:Assertion
.
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miriam-gene:3064
a
ncit:C16612
.
lld:C0393593
a
ncit:C7057
.
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dgn-np:NP475805.RAOEg-tLFPV26JGesBmaKthqUxZ9atuHOFphrAIAGwofI130_assertion
dcterms:description
"[A transgenic primate model for Huntington's Disease (HD) first reported by our group that (HD monkeys) carry the mutant Huntingtin (HTT) gene with expanded polyglutamine (CAG) repeats and, develop chorea, dystonia, and other involuntary motor deficiencies similar to HD [ 1 ].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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miriam-pubmed:23190281
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pav:importedOn
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xsd:date
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dgn-void:source_evidence_literature
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dgn-np:NP475805.RAOEg-tLFPV26JGesBmaKthqUxZ9atuHOFphrAIAGwofI130_publicationInfo
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this:
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xsd:dateTime
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dcterms:rights
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