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An Entity of Type : owl:Axiom, within Data Space : demo.openlinksw.com associated with source document(s)

Attributes	Values
type	Axiom
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
Type	http://purl.obolibrary.org/obo/ECO_0007636 http://purl.obolibrary.org/obo/ECO_0007637 http://purl.obolibrary.org/obo/ECO_0007645 http://purl.obolibrary.org/obo/ECO_0007646
annotatedProperty	http://purl.obolibrary.org/obo/IAO_0000115
annotatedSource	Arts syndrome
annotatedTarget	An X-linked disease that is characterized by profound congenital sensorineural hearing impairment, early-onset hypotonia, delayed motor development, mild to moderate intellectual disability, ataxia, and increased risk of infection and has_material_basis_in mutations of the PRPS1 gene.
database_cross_reference	url:http://ghr.nlm.nih.gov/condition/arts-syndrome url:http://www.ncbi.nlm.nih.gov/books/NBK2591/ url:http://www.omim.org/entry/301835 url:https://www.ncbi.nlm.nih.gov/pubmed/20301738 url:http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=1187&lng=EN
is topic of	Human Disease Ontology

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