Matches in Nanopublications for { ?s ?p "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_provenance.
- NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance.
- NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_provenance.
- assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_provenance.