This HTML5 document contains 26 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n5https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3http://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
n3:DOID_0110160
rdf:type
owl:Class
rdfs:subClassOf
_:vb50942605 _:vb50942606 n3:DOID_0050736 n3:DOID_0050737 n3:DOID_0050539
rdfs:label
Charcot-Marie-Tooth disease axonal type 2T
wdrs:describedby
n5:doid.owl
obo:id
DOID:0110160
obo:hasDbXref
ICD10CM:G60.0 OMIM:617017 ORDO:443950
obo:hasExactSynonym
Charcot-Marie-Tooth neuropathy type 2T AR-CMT2T autosomal recessive axonal Charcot-Marie-Tooth disease type 2T CMT2T
obo:hasOBONamespace
disease_ontology
n3:IAO_0000115
A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.
Subject Item
_:vb50942605
rdf:type
owl:Restriction
owl:onProperty
n3:IDO_0000664
owl:someValuesFrom
n3:GENO_0000147
wdrs:describedby
n5:doid.owl
Subject Item
_:vb50942606
rdf:type
owl:Restriction
owl:onProperty
n3:IDO_0000664
owl:someValuesFrom
n3:GENO_0000148
wdrs:describedby
n5:doid.owl