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_:vb50939283	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A junctional epidermolysis bullosa characterized by skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia and that has_material_basis_in homozygous or compound heterozygous mutation in several genes including COL17A1, ITGB4 and the 3 genes that encode the subunits of laminin-5: LAMA3, LAMB3, and LAMC2. The non-Herlitz type is less severe than the related Herlitz type of junctional epidermolysis bullosa."^^<http://www.w3.org/2001/XMLSchema#string> .
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_:vb50939283	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://www.ncbi.nlm.nih.gov/pubmed/18374450"^^<http://www.w3.org/2001/XMLSchema#string> .
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