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Namespace Prefixes

PrefixIRI
n7https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
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_0110574
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050564
rdfs:label
autosomal dominant nonsyndromic deafness 4B
wdrs:describedby
n7:doid.owl
obo:id
DOID:0110574
obo:hasDbXref
ICD10CM:H90.3 OMIM:614614
obo:hasExactSynonym
autosomal dominant deafness 4B DFNA4B
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CEACAM16 gene on chromosome 19q13.