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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#
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_0110826
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050439
rdfs:label
Usher syndrome type 1
wdrs:describedby
n6:doid.owl
obo:id
DOID:0110826
obo:hasDbXref
OMIM:276900 ORDO:231169 ICD10CM:H35.5
obo:hasExactSynonym
USH1 US1
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa.