Matches in Nanopublications for { ?s ?p "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP963549.RAX_AemMjd0sD49BQyTx4Q4V2tL8Ijs5EvY3cNx-fYUEU130_assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963549.RAX_AemMjd0sD49BQyTx4Q4V2tL8Ijs5EvY3cNx-fYUEU130_provenance.
- NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance.
- assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance.
- NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_provenance.
- NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1117073.RAK4viKR0ezDRY1HkNN61w_t6qB5vDKWhWIaVpoQpTJcI130_provenance.
- NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_provenance.