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:000000470	smad2 sequence variant R133C (human)	hSMAD2/var:R133C|smad2 sequence variant 1 (human)|UniProtKB:Q15796-1, Arg-133, CHEBI:29950		associated_with_disease_progression	DOID:5672	large intestine cancer			PMID:8752209	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011375	20080301	PRO:CNA	
PR:000000470	smad2 sequence variant R133C (human)	hSMAD2/var:R133C|smad2 sequence variant 1 (human)|UniProtKB:Q15796-1, Arg-133, CHEBI:29950		acts_upstream_of_or_within	GO:0007165	signal transduction			PMID:8752209	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011375	20080301	PRO:CNA	
PR:000000470	smad2 sequence variant R133C (human)	hSMAD2/var:R133C|smad2 sequence variant 1 (human)|UniProtKB:Q15796-1, Arg-133, CHEBI:29950	NOT	enables	GO:0003713	transcription coactivator activity			PMID:8752209	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011375	20080301	PRO:CNA