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- Be60e27054808f00ac4470f7a9063a298 NCIT_P378 "NCI" @default.
- Be60e27054808f00ac4470f7a9063a298 type Axiom @default.
- Be60e27054808f00ac4470f7a9063a298 annotatedProperty IAO_0000115 @default.
- Be60e27054808f00ac4470f7a9063a298 annotatedSource NCIT_C178413 @default.
- Be60e27054808f00ac4470f7a9063a298 annotatedTarget "An autosomal dominant condition caused by mutation(s) in the PRRT2 gene, encoding proline-rich transmembrane protein 2. It is characterized by dyskinesia triggered by sudden movement. It shares features with infantile convulsions and paroxysmal choreoathetosis, familial. It is an allelic disorder." @default.