This HTML5 document contains 25 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n6https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3http://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
n3:DOID_0110266
rdf:type
owl:Class
rdfs:subClassOf
n3:DOID_0050736 n3:DOID_0050737 _:vb50942815 n3:DOID_83 _:vb50942816
rdfs:label
cataract 9 multiple types
wdrs:describedby
n6:doid.owl
obo:id
DOID:0110266
obo:hasDbXref
OMIM:604219 ICD10CM:Q12.0
obo:hasExactSynonym
cataract 9 multiple types with or without microcornea CTRCT9
obo:hasNarrowSynonym
CATC1 autosomal recessive congenital cataract 1
obo:hasOBONamespace
disease_ontology
n3:IAO_0000115
A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22.
Subject Item
_:vb50942815
rdf:type
owl:Restriction
owl:onProperty
n3:IDO_0000664
owl:someValuesFrom
n3:GENO_0000147
wdrs:describedby
n6:doid.owl
Subject Item
_:vb50942816
rdf:type
owl:Restriction
owl:onProperty
n3:IDO_0000664
owl:someValuesFrom
n3:GENO_0000148
wdrs:describedby
n6:doid.owl