This HTML5 document contains 16 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n7	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_0060394

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_0060388

rdfs:label

chromosome 15q13.3 microdeletion syndrome

wdrs:describedby

n7:doid.owl

obo:id

DOID:0060394

obo:created_by

elvira

obo:creation_date

2015-09-28T16:23:21Z

obo:hasDbXref

ORDO:199318 ICD10CM:Q93.5 MESH:C567439 OMIM:612001 GARD:10296

obo:hasExactSynonym

15q13.3 microdeletion syndrome

obo:hasOBONamespace

disease_ontology

obo:inSubset

n4:DO_rare_slim

n2:IAO_0000115

A chromosomal deletion syndrome that is characterized by intellectual dsability, developmental delay, autism spectrum disorder and seizure, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15.