This HTML5 document contains 23 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n4https://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_0050540
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050736 _:vb50937083 n2:DOID_0050737 _:vb50937084 n2:DOID_10595
rdfs:label
Charcot-Marie-Tooth disease type 3
rdfs:comment
OMIM mapping confirmed by DO. [SN].
wdrs:describedby
n4:doid.owl
obo:id
DOID:0050540
obo:hasDbXref
OMIM:145900
obo:hasExactSynonym
DEJERINE-SOTTAS NEUROPATHY DEJERINE-SOTTAS SYNDROME
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A Charcot-Marie-Tooth disease that is characterized by motor and sensory peripheral neuropathies caused by demyelination.
Subject Item
_:vb50937083
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n4:doid.owl
Subject Item
_:vb50937084
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n4:doid.owl