Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_assertion type Assertion NP731692.RA6G8ilctz35hNRX6fKbLpx4D6fwEY5chMtNWRERvzzgw130_head.
- 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.