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- NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_assertion type Assertion NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_head.
- NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_assertion wasGeneratedBy ECO_0000203 NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_provenance.
- NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_assertion wasDerivedFrom befree-20140225 NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_provenance.
- NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_assertion SIO_000772 15921863 NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_provenance.
- NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_assertion evidence source_evidence_literature NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_provenance.
- NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360897.RAt-TWpbJCMaoUdzRLyu3YkqvLcglqPNYlpHS-MpkZcZY130_provenance.