Matches in Nanopublications for { ?s ?p "[Mutations in Parkin, an E3 ubiquitin ligase that regulates protein turnover, represent one of the major causes of familial Parkinson disease, a neurodegenerative disorder characterized by the loss of dopaminergic neurons and impaired mitochondrial functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP878005.RA1lYY3qL5qYtRG6gD4sVUK3aVl4-2wSB7tTiEjIKeuQM130_assertion description "[Mutations in Parkin, an E3 ubiquitin ligase that regulates protein turnover, represent one of the major causes of familial Parkinson disease, a neurodegenerative disorder characterized by the loss of dopaminergic neurons and impaired mitochondrial functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP878005.RA1lYY3qL5qYtRG6gD4sVUK3aVl4-2wSB7tTiEjIKeuQM130_provenance.
- NP633425.RAOnosR0yruIDsbDJnnHXf1elOq-awan5KYZBPonZSB3o130_assertion description "[Mutations in Parkin, an E3 ubiquitin ligase that regulates protein turnover, represent one of the major causes of familial Parkinson disease, a neurodegenerative disorder characterized by the loss of dopaminergic neurons and impaired mitochondrial functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633425.RAOnosR0yruIDsbDJnnHXf1elOq-awan5KYZBPonZSB3o130_provenance.
- NP843304.RAKuX0KpGB7J_ZXzQXwYoaNTtRXzzI5JcdK-I-dFEaqLg130_assertion description "[Mutations in Parkin, an E3 ubiquitin ligase that regulates protein turnover, represent one of the major causes of familial Parkinson disease, a neurodegenerative disorder characterized by the loss of dopaminergic neurons and impaired mitochondrial functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843304.RAKuX0KpGB7J_ZXzQXwYoaNTtRXzzI5JcdK-I-dFEaqLg130_provenance.