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_:vb50939548	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A hypomagnesemia characterized by autosomal recessive inheritance of excessive urinary Ca(2+) and Mg(2+) excretion that has material_basis_in homozygous or compound heterozygous mutation in the CLDN16 gene on chromosome 3q28."^^<http://www.w3.org/2001/XMLSchema#string> .
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_:vb50939548	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007645> .
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_:vb50939548	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0060880> .