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- B9dd20bc207ee2f6a78502d7803389fb6 NCIT_P378 "NCI" @default.
- B9dd20bc207ee2f6a78502d7803389fb6 type Axiom @default.
- B9dd20bc207ee2f6a78502d7803389fb6 annotatedProperty IAO_0000115 @default.
- B9dd20bc207ee2f6a78502d7803389fb6 annotatedSource NCIT_C128145 @default.
- B9dd20bc207ee2f6a78502d7803389fb6 annotatedTarget "An autosomal recessive disorder caused by mutation(s) in the LAMB2 gene, encoding laminin subunit beta-2. It is characterized by congenital nephrotic syndrome with diffuse mesangial sclerosis and distinct ocular abnormalities." @default.