Compare GO annotations related to Carnitine deficiency, systemic primary using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0015226carnitine transporter activity RGD:3702IDARatRGD:730132|PMID:9792817
Molecular FunctionGO:0015651quaternary ammonium group transmembrane transporter activity RGD:3702IMPRatRGD:70011|PMID:10454528
Biological ProcessGO:0015879carnitine transport RGD:3702IDARatRGD:730132|PMID:9792817
Biological ProcessGO:0015697quaternary ammonium group transport RGD:3702IMPRatRGD:70011|PMID:10454528