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An Entity of Type : owl:Axiom, within Data Space : linkeddata.uriburner.com:28898 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_0007645
annotatedProperty	http://purl.obolibrary.org/obo/IAO_0000115
annotatedSource	blue color blindness
annotatedTarget	A color blindness that is characterised by a selective deficiency of blue vision, has_material_basis_in autosomal dominant inheritance of a mutation in the OPN1SW gene and is associated with a deficiency or absence of blue-sensitive cone photoreceptor function.
database_cross_reference	url:http://www.omim.org/entry/190900 url:https://www.ncbi.nlm.nih.gov/pubmed/2788922 url:http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=88629
is topic of	Human Disease Ontology

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