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owl:sameAs
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About:
congenital nystagmus 3
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An Entity of Type :
wikibase:Item
, within Data Space :
wikidata.demo.openlinksw.com
associated with source
document(s)
Type:
Item
New Facet based on Instances of this Class
human disease
Attributes
Values
rdf:type
Item
description
human disease
(en)
մարդու հիվանդություն
(hy)
хвороба людини
(uk)
exact match
wds:Q102294560-324780FB-4B6D-4813-A8B0-D8C9F0FE36ED
wds:Q102294560-AAA12274-AA9E-40A8-9D09-EB765F7D8A8F
exact match
http://purl.obolibrary.org/obo/DOID_0111793
http://identifiers.org/doid/DOID:0111793
Disease Ontology ID
wds:Q102294560-B119E379-73CC-45EF-8AF1-EFCBF50BBB60
Disease Ontology ID
http://purl.obolibrary.org/obo/DOID_DOID:0111793
Disease Ontology ID
DOID:0111793
rdfs:label
congenital nystagmus 3
(en)
skos:prefLabel
congenital nystagmus 3
(en)
name
congenital nystagmus 3
(en)
instance of
wds:Q102294560-15BF7647-F1E9-474E-9C5C-D242BC07BC3C
instance of
class of disease
subclass of
wds:Q102294560-36BBE5BD-606A-4ECC-86AF-2E91DFA489D8
wds:Q102294560-FDA18362-C8B5-4BCB-9287-24AF9EA11B1B
subclass of
autosomal dominant disease
congenital nystagmus
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q102294560
Faceted Search & Find service v1.16.117 as of May 05 2024
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