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:000000298	pituitary homeobox 2 sequence variant R89W (human)	hPITX2/var:R89W|pituitary homeobox 2 sequence variant 1 (human)|UniProtKB:Q99697-1, Arg-89, CHEBI:29954		associated_with_disease_progression	DOID:0050786	iridogoniodysgenesis syndrome			PMID:9437321	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_003762	20080301	PRO:CNA