Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP523312.RAQ9lr0R2KbL4h7_OWKCZ3Qq1-Pkdhn4VB67Kww8_ufpg130_assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523312.RAQ9lr0R2KbL4h7_OWKCZ3Qq1-Pkdhn4VB67Kww8_ufpg130_provenance.
• NP523358.RAQR7mDDyXni-MjiZOng3kOOUOEBkBnQS9syjkRMM7-kQ130_assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523358.RAQR7mDDyXni-MjiZOng3kOOUOEBkBnQS9syjkRMM7-kQ130_provenance.
• NP523446.RAfDhRcJ6YKZa9rSRVw-uwHBZrYJ0h-MX7O2WUd7-x1OE130_assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523446.RAfDhRcJ6YKZa9rSRVw-uwHBZrYJ0h-MX7O2WUd7-x1OE130_provenance.
• NP523458.RATZF7Gf3bejasMeBFoiBZEEt_myQhorQpHaBfAO4I9Yc130_assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523458.RATZF7Gf3bejasMeBFoiBZEEt_myQhorQpHaBfAO4I9Yc130_provenance.
• assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1021645.RAZDlDq_NR9JN2rXOYnwysOsune7lYJkER2WH9MKZImEw130_assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021645.RAZDlDq_NR9JN2rXOYnwysOsune7lYJkER2WH9MKZImEw130_provenance.
• NP1021651.RAYxCdsuanmPtWDUxcBaELLEbIkMD-xNOQQ4GgLb2AmXg130_assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021651.RAYxCdsuanmPtWDUxcBaELLEbIkMD-xNOQQ4GgLb2AmXg130_provenance.
• NP1021649.RAvTow7lQLdHgmNSuiUfJiFCPOHPfvodLUNTPqL_Uav0A130_assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021649.RAvTow7lQLdHgmNSuiUfJiFCPOHPfvodLUNTPqL_Uav0A130_provenance.
• NP523331.RA9LQFo8NmWgCNAjNxEBXVgHHpHGelxVeLKeZBVFRuv7I130_assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523331.RA9LQFo8NmWgCNAjNxEBXVgHHpHGelxVeLKeZBVFRuv7I130_provenance.
• NP1021653.RAFMY1ru2TpFe194G5602hUGZBHB92TGIEcXwG1Q9OCMg130_assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021653.RAFMY1ru2TpFe194G5602hUGZBHB92TGIEcXwG1Q9OCMg130_provenance.
• NP1021648.RA09g5jqWJ_fDOcL6HI7CXSmXGnvOkbD8s57g3wPoi-mY130_assertion description "[PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021648.RA09g5jqWJ_fDOcL6HI7CXSmXGnvOkbD8s57g3wPoi-mY130_provenance.