Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP380992.RAbe5kERMmnXy_wn3oL_7zAX0uPfiZY_L52LBHmMp9P1s130_assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380992.RAbe5kERMmnXy_wn3oL_7zAX0uPfiZY_L52LBHmMp9P1s130_provenance.
• NP871976.RAUuOcApqL_IIthDysX5TjyJX0KAfLwBTfE_uxGsNGt64130_assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871976.RAUuOcApqL_IIthDysX5TjyJX0KAfLwBTfE_uxGsNGt64130_provenance.
• NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_provenance.
• NP573569.RA15UUD-kyWw4WBvyMj8fSOtgQCfPfBymbun5hyjpEA6o130_assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP573569.RA15UUD-kyWw4WBvyMj8fSOtgQCfPfBymbun5hyjpEA6o130_provenance.
• NP710157.RAB12EgomtJIBO3_AXTZRVzNEBGJmhC_YBSmf_PxQyPxM130_assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710157.RAB12EgomtJIBO3_AXTZRVzNEBGJmhC_YBSmf_PxQyPxM130_provenance.
• NP856472.RA8KZ4gVKwX3ZS48diLOPpJD9ufDeb6CMBuh3iRzbgrQ4130_assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856472.RA8KZ4gVKwX3ZS48diLOPpJD9ufDeb6CMBuh3iRzbgrQ4130_provenance.
• NP1011709.RA5Rvx_tbV_Kt3uIny5N5WmvGjk2VevhlCbetUzW1SvwA130_assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011709.RA5Rvx_tbV_Kt3uIny5N5WmvGjk2VevhlCbetUzW1SvwA130_provenance.
• NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance.
• NP1011708.RAVV4me9Md6azVYfasgjiF__Nx3KHi-o-DXrX7GkmS6w4130_assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011708.RAVV4me9Md6azVYfasgjiF__Nx3KHi-o-DXrX7GkmS6w4130_provenance.
• assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.