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Namespace Prefixes

PrefixIRI
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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#
n7http://purl.obolibrary.org/obo/doid#
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_0060283
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_37
rdfs:label
peeling skin syndrome
rdfs:comment
NT MGI.
wdrs:describedby
n6:doid.owl
obo:id
DOID:0060283
obo:created_by
emitraka
obo:creation_date
2015-02-04T16:28:52Z
obo:hasDbXref
OMIM:270300 ORDO:263543 ICD10CM:Q80.8 OMIM:613088
obo:hasOBONamespace
disease_ontology
obo:inSubset
n7:DO_rare_slim
n2:IAO_0000115
A skin disease that is characterized by the painless peeling of the top layer of skin predominately on the hands and feet, has_material_basis_in autosomal recessive inheritance of mutation in the TGM5 gene and/pr CSTA gene.