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- NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_assertion type Assertion NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_head.
- NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_assertion description "[The clinical features of severe myoclonic epilepsy of infancy (SMEI) resemble those of mitochondrial diseases, although most patients have the sodium channel (SCN1A) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_provenance.
- NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_assertion evidence source_evidence_literature NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_provenance.
- NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_assertion SIO_000772 19359143 NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_provenance.
- NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_assertion wasDerivedFrom befree-20140225 NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_provenance.
- NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_assertion wasGeneratedBy ECO_0000203 NP476325.RA2N37F8t7r4U9InC-RB9XA4RuLOmQ5aS3TKR-qF0_4lQ130_provenance.