Matches in Nanopublications for { ?s ?p "[The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1003933.RAgJVc2cJvWsb5MEsVTtBSE3cP50OxTAwBrVASrdzmsfQ130_assertion description "[The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1003933.RAgJVc2cJvWsb5MEsVTtBSE3cP50OxTAwBrVASrdzmsfQ130_provenance.
- NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_assertion description "[The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance.