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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_0110059
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_2187
rdfs:label
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
wdrs:describedby
n7:doid.owl
obo:id
DOID:0110059
obo:hasDbXref
ICD10CM:K00.5 OMIM:301201
obo:hasExactSynonym
AIH3 amelogenesis imperfecta type IE X-linked 2 amelogenesis imperfecta 3 hypoplastic type
obo:hasOBONamespace
disease_ontology
obo:hasRelatedSynonym
X-linked enamel hypoplasia
n2:IAO_0000115
An amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region.