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:000000872	voltage-gated potassium channel subunit KCNQ1 sequence variant R243H (human)	hKCNQ1/var:R243H|UniProtKB:P51787-1, Arg-243, CHEBI:29979|voltage-gated potassium channel subunit KCNQ1 sequence variant 6 (human)		associated_with_disease_progression	DOID:2842	Jervell-Lange Nielsen syndrome			PMID:10728423	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_008941	20080601	PRO:CNA	
PR:000000872	voltage-gated potassium channel subunit KCNQ1 sequence variant R243H (human)	hKCNQ1/var:R243H|UniProtKB:P51787-1, Arg-243, CHEBI:29979|voltage-gated potassium channel subunit KCNQ1 sequence variant 6 (human)		part_of	GO:0008076	voltage-gated potassium channel complex			PMID:10728423	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_008941	20080601	PRO:CNA	
PR:000000872	voltage-gated potassium channel subunit KCNQ1 sequence variant R243H (human)	hKCNQ1/var:R243H|UniProtKB:P51787-1, Arg-243, CHEBI:29979|voltage-gated potassium channel subunit KCNQ1 sequence variant 6 (human)	decreased|contributes_to	enables	GO:0005251	delayed rectifier potassium channel activity	PR:000002622		PMID:10728423	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_008941	20080601	PRO:CNA