Matches in Nanopublications for { ?s ?p "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_provenance.
- NP5735.RAJBMwny45dGcaVC4nsjwg_3S37M-ZDpqy1FB1IimrLjw130_assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5735.RAJBMwny45dGcaVC4nsjwg_3S37M-ZDpqy1FB1IimrLjw130_provenance.
- NP226050.RAYtxybT4d4GFfT06hnfyCDTyXHq1Rs0dsIb6aBFh_Ylg130_assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226050.RAYtxybT4d4GFfT06hnfyCDTyXHq1Rs0dsIb6aBFh_Ylg130_provenance.
- NP106018.RAaC5VLItyB6hUY_a8DDkGJAFkfb5lxlUnMnv24OR1t2E130_assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106018.RAaC5VLItyB6hUY_a8DDkGJAFkfb5lxlUnMnv24OR1t2E130_provenance.
- assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP597932.RAk1uJMdqrghe3ZGdYE6_AAHDneYhx-RiujHFOfKUH8HI130_assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597932.RAk1uJMdqrghe3ZGdYE6_AAHDneYhx-RiujHFOfKUH8HI130_provenance.
- NP85803.RAIIChmKEegrATYJha1PkPlginAx3rd8ro9aU9vGhYMxc130_assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85803.RAIIChmKEegrATYJha1PkPlginAx3rd8ro9aU9vGhYMxc130_provenance.
- NP4912.RALjJEJzwc_500V3BY6voegmvECdnrHxC0Hu3WfcmywRI130_assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4912.RALjJEJzwc_500V3BY6voegmvECdnrHxC0Hu3WfcmywRI130_provenance.
- NP597931.RA0VPCR_EzkLG4xy5vRCmYu2xJFkz_XBi1dbMB_qXQJ2s130_assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597931.RA0VPCR_EzkLG4xy5vRCmYu2xJFkz_XBi1dbMB_qXQJ2s130_provenance.