PRO_ID	Object_term	Object_syny	Modifier	Relation	Ontology_ID	Ontology_term	Relative_to	Interaction_with	Evidence_source	Evidence_code	Taxon	Inferred_from	DB_ID	Date	Assigned_by	Comment
PR:000000808	voltage-gated potassium channel KCNV2 sequence variant W188C (human)	hKCNV2/var:W188C|UniProtKB:Q8TDN2, Trp-188, CHEBI:29950|voltage-gated potassium channel KCNV2 sequence variant 6 (human)		associated_with_disease_progression	DOID:0050795	cone dystrophy			PMID:16909397	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_027633	20080601	PRO:CNA