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_:vb50946129	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A syndrome characterized by retinitis pigmentosa and recurrent respiratory infections with nasal ciliary abnormalities and hearing loss in some patients that has_material_basis_in mutation in RPGR on chromosome Xp11.4."^^<http://www.w3.org/2001/XMLSchema#string> .
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