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