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

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Namespace Prefixes

Prefix	IRI
n6	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#
n8	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_13501

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_1756 _:vb50949046

rdfs:label

Mobius syndrome

rdfs:comment

OMIM mapping confirmed by DO. [SN].

wdrs:describedby

n6:doid.owl

obo:id

DOID:13501

obo:hasDbXref

GARD:8549 SNOMEDCT_US_2021_09_01:89444000 MESH:D020331 OMIM:157900 ICD10CM:Q87.0 UMLS_CUI:C0221060 NCI:C84893

obo:hasExactSynonym

Moebius congenital oculofacial paralysis Oromandibular-limb hypogenesis spectrum

obo:hasOBONamespace

disease_ontology

obo:inSubset

n8:NCIthesaurus

n2:IAO_0000115

A facial nerve disease characterized by congenital, uni- or bilateral, non-progressive facial weakness and limited abduction of the eye(s).

Subject Item

_:vb50949046

rdf:type

owl:Restriction

owl:onProperty

n2:RO_0002452

owl:someValuesFrom

n2:SYMP_0000094

wdrs:describedby

n6:doid.owl