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Matches in Nanopublications for { ?s ?p "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1158224.RAQ09-TZpTH5lRnc9HXoZ_OlfUGXQWBJTuHYC3VJv6eGo130_assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158224.RAQ09-TZpTH5lRnc9HXoZ_OlfUGXQWBJTuHYC3VJv6eGo130_provenance.
• NP1158222.RAAtWp6PbzgsS_J_jb-PFs8fK3oNNa_csgyXkoS755-NU130_assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158222.RAAtWp6PbzgsS_J_jb-PFs8fK3oNNa_csgyXkoS755-NU130_provenance.
• NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_provenance.
• NP682524.RAp8Z8gxTkuOEDtGtJDVoAVzx665V4j_18oZKALI_aswA130_assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682524.RAp8Z8gxTkuOEDtGtJDVoAVzx665V4j_18oZKALI_aswA130_provenance.
• NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_provenance.
• NP682537.RAw6K82-YSiKsSkKxGjK3ARCYne3LH2el_csuirZA4X7A130_assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682537.RAw6K82-YSiKsSkKxGjK3ARCYne3LH2el_csuirZA4X7A130_provenance.
• NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_provenance.
• NP1158223.RA-F4Jc4uecAhzjLfEnyKQxYmWDObiyDghff6aqmEGdiQ130_assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158223.RA-F4Jc4uecAhzjLfEnyKQxYmWDObiyDghff6aqmEGdiQ130_provenance.