Matches in Nanopublications for { ?s ?p "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance.
- NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_provenance.
- NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_provenance.
- NP227904.RA8if0YPwfHEjXp8-ZHUMy25sBDo4LyUQv3qviC5J14fE130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227904.RA8if0YPwfHEjXp8-ZHUMy25sBDo4LyUQv3qviC5J14fE130_provenance.
- NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_provenance.
- NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance.
- NP1102138.RAxbu5pQbL3k2ffxApRIqpmgHwVOFbF1iaQFfUyI-YDXE130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102138.RAxbu5pQbL3k2ffxApRIqpmgHwVOFbF1iaQFfUyI-YDXE130_provenance.
- NP1102141.RA9PYFg4BINTyoVPkWk5P_WpHDT7tAAxhX8-AiV8bSlxI130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102141.RA9PYFg4BINTyoVPkWk5P_WpHDT7tAAxhX8-AiV8bSlxI130_provenance.