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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_0110230
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_83
rdfs:label
cataract 34 multiple types
wdrs:describedby
n7:doid.owl
obo:id
DOID:0110230
obo:hasDbXref
ICD10CM:Q12.0 OMIM:612968
obo:hasExactSynonym
cataract 34 multiple types with or without microcornea CATC3 CTRCT34 autosomal recessive congenital cataract 3
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A cataract that has_material_basis_in variation in the region 1p34.3-p32.2.