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Matches in Nanopublications for { ?s ?p "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_provenance.
• assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1158087.RAYv27OWt9DkfF1MID9Q7S8RLS5s_5DpYOFpYDe8Luk0c130_assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158087.RAYv27OWt9DkfF1MID9Q7S8RLS5s_5DpYOFpYDe8Luk0c130_provenance.
• NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance.
• NP1158089.RACMPENd0QGgXQQZo9ScRoZSoWqQx_RdZFCxI_gYZedQE130_assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158089.RACMPENd0QGgXQQZo9ScRoZSoWqQx_RdZFCxI_gYZedQE130_provenance.
• NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance.
• NP650759.RAyKtE3Hrmk0lvKOzIaBuWReKBnjejZULJsENiaf-sS0Q130_assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650759.RAyKtE3Hrmk0lvKOzIaBuWReKBnjejZULJsENiaf-sS0Q130_provenance.