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Namespace Prefixes

PrefixIRI
n6https://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_0110975
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050581
rdfs:label
brachydactyly type B2
wdrs:describedby
n6:doid.owl
obo:id
DOID:0110975
obo:hasDbXref
ICD10CM:Q73.8 ORDO:140908 OMIM:611377
obo:hasExactSynonym
BDB2
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A brachydactyly characterized by hypoplasia/aplasia of distal phalanges, distal symphalangism, fusion of carpal/tarsal bones, and partial cutaneous syndactyly that has_material_basis_in mutations in the NOG gene on chromosome 17q22.