PR:000000116	noggin sequence variant Y222D (human)	hNOG/var:Y222D|noggin sequence variant 9 (human)|UniProtKB:Q13253, Tyr-222, CHEBI:29958		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:10080184	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011366	20080301	PRO:CNA