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

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

Prefix	IRI
n3	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n4	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n4:DOID_0110179

rdf:type

owl:Class

rdfs:subClassOf

n4:DOID_0050539 _:vb50942644 n4:DOID_0050737

rdfs:label

Charcot-Marie-Tooth disease type 2B2

wdrs:describedby

n3:doid.owl

obo:id

DOID:0110179

obo:hasDbXref

ORDO:101101 OMIM:605589 ICD10CM:G60.0

obo:hasExactSynonym

Autosomal recessive axonal CMT4C3 ARCMT2B AR-CMT2B2 Charcot-Marie-Tooth disease neuronal type 2B2 Charcot-Marie-Tooth neuropathy type 2B2 autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2 CMT2B2

obo:hasOBONamespace

disease_ontology

n4:IAO_0000115

A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous mutation in the MED25 gene.

Subject Item

_:vb50942644

rdf:type

owl:Restriction

owl:onProperty

n4:IDO_0000664

owl:someValuesFrom

n4:GENO_0000148

wdrs:describedby

n3:doid.owl