Matches in DBpedia 2016-04 for { ?s ?p "Kv7.2 (KvLQT2) is a potassium channel protein coded for by the gene KCNQ2.It is associated with benign familial neonatal epilepsy.The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins."@en }
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- KvLQT2 comment "Kv7.2 (KvLQT2) is a potassium channel protein coded for by the gene KCNQ2.It is associated with benign familial neonatal epilepsy.The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins.".
- Q14914307 comment "Kv7.2 (KvLQT2) is a potassium channel protein coded for by the gene KCNQ2.It is associated with benign familial neonatal epilepsy.The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins.".