This HTML5 document contains 22 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n4https://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_0110831
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0110826 _:vb50943744 _:vb50943745 n2:DOID_0080578
rdfs:label
Usher syndrome type 1D
wdrs:describedby
n4:doid.owl
obo:id
DOID:0110831
obo:hasDbXref
OMIM:601067 ICD10CM:H35.5
obo:hasExactSynonym
USH1D Usher syndrome type ID
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22.
Subject Item
_:vb50943744
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n4:doid.owl
Subject Item
_:vb50943745
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000930
wdrs:describedby
n4:doid.owl