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:000000108	noggin sequence variant P223L (human)	hNOG/var:P223L|noggin sequence variant 10 (human)|UniProtKB:Q13253, Pro-223, CHEBI:30006		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:10080184	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011367	20080301	PRO:CNA