This HTML5 document contains 22 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
n8	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	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#
n4	http://purl.obolibrary.org/obo/doid#
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

n2:DOID_0060378

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_4501 n2:DOID_0080012 _:vb50938744

rdfs:label

orofaciodigital syndrome VIII

wdrs:describedby

n8:doid.owl

obo:id

DOID:0060378

obo:created_by

elvira

obo:creation_date

2015-09-18T15:00:19Z

obo:hasDbXref

MESH:C557820 ORDO:2755 OMIM:300484 UMLS_CUI:C0796101

obo:hasExactSynonym

Edwards syndrome OFD8

obo:hasOBONamespace

disease_ontology

obo:inSubset

n4:DO_rare_slim

n2:IAO_0000115

An orofaciodigital syndrome that is characterized by tongue lobulation, hypoplasia of the epiglottis, cleft lip, polydactyly, short stature and intellectual deficit, and has_material_basis_in X-linked recessive inheritance.

Subject Item

_:vb50938744

rdf:type

owl:Restriction

owl:onProperty

n2:IDO_0000664

owl:someValuesFrom

n2:GENO_0000149

wdrs:describedby

n8:doid.owl