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Namespace Prefixes

PrefixIRI
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n6http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
dchttp://purl.org/dc/elements/1.1/
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
_:vb50942070
rdf:type
owl:Axiom
wdrs:describedby
n5:doid.owl
dc:type
n6:ECO_0007645
owl:annotatedProperty
n6:IAO_0000115
owl:annotatedSource
n6:DOID_0090020
owl:annotatedTarget
A bone development disease characterized by malformation of the central rays of the autopod and presenting with syndactyly, median clefts of the hands and feet, and aplasia and/or hypoplasia of the phalanges, metacarpals, and metatarsals. Some patients also have mental retardation, ectodermal and craniofacial findings, and orofacial clefting.
obo:hasDbXref
url:https://www.ncbi.nlm.nih.gov/pubmed/12668597 url:https://www.ncbi.nlm.nih.gov/pubmed/7802032