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- NP415747.RAXZ_ZBXRKD1L4sTPkHJ_5X4eoQXrNHSXlwrdzJnYaM4Y130_assertion type Assertion NP415747.RAXZ_ZBXRKD1L4sTPkHJ_5X4eoQXrNHSXlwrdzJnYaM4Y130_head.
- NP415747.RAXZ_ZBXRKD1L4sTPkHJ_5X4eoQXrNHSXlwrdzJnYaM4Y130_assertion description "[Progressive myoclonus epilepsy 1 (EPM1) or Unverricht-Lundborg disease is a human autosomal recessive neurodegenerative disorder caused by mutations in cystatin B (CSTB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415747.RAXZ_ZBXRKD1L4sTPkHJ_5X4eoQXrNHSXlwrdzJnYaM4Y130_provenance.
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- NP415747.RAXZ_ZBXRKD1L4sTPkHJ_5X4eoQXrNHSXlwrdzJnYaM4Y130_assertion SIO_000772 14526183 NP415747.RAXZ_ZBXRKD1L4sTPkHJ_5X4eoQXrNHSXlwrdzJnYaM4Y130_provenance.
- NP415747.RAXZ_ZBXRKD1L4sTPkHJ_5X4eoQXrNHSXlwrdzJnYaM4Y130_assertion wasDerivedFrom befree-2016 NP415747.RAXZ_ZBXRKD1L4sTPkHJ_5X4eoQXrNHSXlwrdzJnYaM4Y130_provenance.
- NP415747.RAXZ_ZBXRKD1L4sTPkHJ_5X4eoQXrNHSXlwrdzJnYaM4Y130_assertion wasGeneratedBy ECO_0000203 NP415747.RAXZ_ZBXRKD1L4sTPkHJ_5X4eoQXrNHSXlwrdzJnYaM4Y130_provenance.