About: nodeID://b50937076

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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 http://purl.obolibrary.org/obo/ECO_0007646
annotatedProperty	http://purl.obolibrary.org/obo/IAO_0000115
annotatedSource	congenital stationary night blindness
annotatedTarget	A hereditary night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves.
database_cross_reference	url:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1772254/ url:http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=215 url:http://www.ncbi.nlm.nih.gov/books/NBK1245/ url:http://www.omim.org/entry/610444 url:http://disorders.eyes.arizona.edu/disorders/night-blindness-congenital-stationary-csnbad3
is topic of	Human Disease Ontology

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