Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_assertion type Assertion NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_head.
- NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_assertion description "[Mutations in the CHRNA4 or CHRNB subunits of the neuronal nicotinic acetylcholine receptor lead to familial nocturnal frontal lobe epilepsy, while defects in the voltage-gated potassium channels KCNQ2 and KCNQ3 have recently been found to cause benign familial neonatal convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_provenance.
- NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_assertion evidence source_evidence_literature NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_provenance.
- NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_assertion SIO_000772 11888238 NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_provenance.
- NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_assertion wasDerivedFrom befree-20140225 NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_provenance.
- NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_assertion wasGeneratedBy ECO_0000203 NP477409.RAggKcIEDNmfSTGI1j2E4NYNjgWH8IeRQKSztio9tk85E130_provenance.