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	Protein _region	Modified_residue, MOD_ID	Date	Assigned_by	Equivalent_Form	Comment	Protein_Features
PR:000026111	methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial sequence variant MCCA D532H (human)			agent_in	MIM:210200	3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY			PMID:11181649	EXP	TaxID:9606					20101130	PRO:CNA		Severe form of disease.	
PR:000026111	methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial sequence variant MCCA D532H (human)			has_agent	SO:0001630	splice_region_variant			PMID:11181649	EXP	TaxID:9606					20101130	PRO:CNA