This HTML5 document contains 17 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

Prefix	IRI
n7	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_0110838

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_0110827 _:vb50943758

rdfs:label

Usher syndrome type 2A

wdrs:describedby

n7:doid.owl

obo:id

DOID:0110838

obo:hasDbXref

OMIM:276901 ICD10CM:H35.5 GARD:5440

obo:hasExactSynonym

Usher syndrome type IIA USH2A

obo:hasOBONamespace

disease_ontology

n2:IAO_0000115

An Usher syndrome type 2 characterized by moderate to severe sensorineural hearing loss, mainly affecting perception of high frequency sounds and progressive retinitis pigmentosa that has_material_basis_in homozygous or compound heterozygous mutation in the USH2A gene on chromosome 1q41.

Subject Item

_:vb50943758

rdf:type

owl:Restriction

owl:onProperty

n2:IDO_0000664

owl:someValuesFrom

n2:GENO_0000148

wdrs:describedby

n7:doid.owl