Compare GO annotations related to Night blindness, congenital stationary, type 1 using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Cellular ComponentGO:0005622intracellular Q9GZU5IEPHumanPMID:11062471
Biological ProcessGO:0007601visual perception MGI:2448607IMPMouseMGI:MGI:2447963|PMID:12506099