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Namespace Prefixes

Prefix	IRI
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n4	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
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

_:vb50941489

rdf:type

owl:Axiom

wdrs:describedby

n6:doid.owl

owl:annotatedProperty

n4:IAO_0000115

owl:annotatedSource

n4:DOID_0080713

owl:annotatedTarget

A syndrome that has_material_basis_in an extra copy of the MECP2 gene in each cell, occurs almost exclusively in males and that is characterized by delayed development of motor skills such as sitting and walking.

obo:hasDbXref

url:https://ghr.nlm.nih.gov/condition/mecp2-duplication-syndrome url:https://rarediseases.info.nih.gov/diseases/9781/mecp2-duplication-syndrome