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Namespace Prefixes

PrefixIRI
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n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
n5http://purl.obolibrary.org/obo/doid#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_0110828
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050439
rdfs:label
Usher syndrome type 3
wdrs:describedby
n8:doid.owl
obo:id
DOID:0110828
obo:hasDbXref
GARD:5442 ORDO:231183 NCI:C126329 MESH:D052245
obo:hasExactSynonym
USH3
obo:hasOBONamespace
disease_ontology
obo:inSubset
n5:NCIthesaurus
n2:IAO_0000115
An Usher syndrome characterized by progressive hearing loss typically beginning in late childhood, variable vestibular dysfunction and onset of retinitis pigmentosa by the second decade of life.