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Namespace Prefixes

PrefixIRI
n5https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n6http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
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
_:vb50948486
rdf:type
owl:Axiom
wdrs:describedby
n5:doid.owl
owl:annotatedProperty
n6:IAO_0000115
owl:annotatedSource
n6:DOID_12580
owl:annotatedTarget
A syndrome that has_material_basis_in deletion of the end of the chromosome 5 p arm and that is characterized by intellectual disability, delayed development, small head size, low birth weight, weak muscle tone widely set eyes, low-set ears, a small jaw, a rounded face and a high-pitched cry that sounds like that of a cat.
obo:hasDbXref
url:https://ghr.nlm.nih.gov/condition/cri-du-chat-syndrome