Matches in Nanopublications for { ?s ?p "[SCN2A gene mutations are associated with inherited benign neonatal-infantile epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_assertion description "[SCN2A gene mutations are associated with inherited benign neonatal-infantile epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126971.RALgI8q3xF4qbQQWaXP1uuc0GNtE05i1E2ZZ0vtRH3YoI130_provenance.
- assertion description "[SCN2A gene mutations are associated with inherited benign neonatal-infantile epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_assertion description "[SCN2A gene mutations are associated with inherited benign neonatal-infantile epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190152.RAsiG8rvjOQd1MJplL_dkf4ncw50reiPxAZTgKdzmf_jk130_provenance.
- NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_assertion description "[SCN2A gene mutations are associated with inherited benign neonatal-infantile epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance.