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- source_evidence_literature type ECO_0000212 NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_provenance.
- NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_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." NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_provenance.
- NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_assertion evidence source_evidence_literature NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_provenance.
- NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_assertion SIO_000772 19359143 NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_provenance.
- NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_assertion wasDerivedFrom befree-2016 NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_provenance.
- NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_assertion wasGeneratedBy ECO_0000203 NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_provenance.
- befree-2016 importedOn "2016-02-19" NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_provenance.