Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion> ?p ?o ?g. }
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- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion type Assertion NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_head.
- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_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." NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion evidence source_evidence_literature NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion SIO_000772 11888238 NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion wasDerivedFrom befree-20140225 NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion wasGeneratedBy ECO_0000203 NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.