Matches in Nanopublications for { ?s ?p "[Mutations in RYR1 are associated with several congenital myopathies (termed RYR1-related myopathies) that are the most common non-dystrophic muscle diseases of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_assertion description "[Mutations in RYR1 are associated with several congenital myopathies (termed RYR1-related myopathies) that are the most common non-dystrophic muscle diseases of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_provenance.
- assertion description "[Mutations in RYR1 are associated with several congenital myopathies (termed RYR1-related myopathies) that are the most common non-dystrophic muscle diseases of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP676939.RAPouADzeNYe216sBAedEZ_NwoGblNY6ZbqBrboui-lo8130_assertion description "[Mutations in RYR1 are associated with several congenital myopathies (termed RYR1-related myopathies) that are the most common non-dystrophic muscle diseases of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676939.RAPouADzeNYe216sBAedEZ_NwoGblNY6ZbqBrboui-lo8130_provenance.
- NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_assertion description "[Mutations in RYR1 are associated with several congenital myopathies (termed RYR1-related myopathies) that are the most common non-dystrophic muscle diseases of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance.