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Namespace Prefixes

Prefix	IRI
n7	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
dc	http://purl.org/dc/elements/1.1/
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

_:vb50946423

rdf:type

owl:Axiom

wdrs:describedby

n7:doid.owl

dc:type

n3:ECO_0007645

owl:annotatedProperty

n3:IAO_0000115

owl:annotatedSource

n3:DOID_0112276

owl:annotatedTarget

A movement disease characterized by delayed psychomotor development and infantile or childhood onset of hyperkinetic involuntary movements, including chorea and athetosis that has_material_basis_in heterozygous mutation of GNAO1 on chromosome 16q13.

obo:hasDbXref

url:https://pubmed.ncbi.nlm.nih.gov/28357411/ url:https://pubmed.ncbi.nlm.nih.gov/27068059/