This HTML5 document contains 16 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
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#
n7	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_0060411

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_0060388

rdfs:label

chromosome 1q21.1 deletion syndrome

wdrs:describedby

n6:doid.owl

obo:id

DOID:0060411

obo:created_by

elvira

obo:creation_date

2015-09-28T17:17:38Z

obo:hasDbXref

OMIM:612474 GARD:10813 ICD10CM:Q93.5 ORDO:250989

obo:hasExactSynonym

1q21.1 microdeletion syndrome

obo:hasOBONamespace

disease_ontology

obo:hasRelatedSynonym

monosomy 1q21.1

obo:inSubset

n7:DO_rare_slim

n2:IAO_0000115

A chromosomal deletion syndrome that has_material_basis_in a contiguous deletion of the 1q21.1 region on chromosome 1 and is characterized by an increases the risk of delayed development, intellectual disability, physical abnormalities, and neurological and psychiatric problems.