Matches in Nanopublications for { ?s ?p "[Mutations in C-terminal titin cause autosomal dominant tibial muscular dystrophy (TMD) as reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP837442.RABhtPqPWzYozMz6YVfK8te_AOXM34yxNodjZt5y_S7NM130_assertion description "[Mutations in C-terminal titin cause autosomal dominant tibial muscular dystrophy (TMD) as reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837442.RABhtPqPWzYozMz6YVfK8te_AOXM34yxNodjZt5y_S7NM130_provenance.
- NP379264.RAKVEJImpbwvfO0gu2yc_Z47GZ-dQFuRXcKgM7Hex5_k4130_assertion description "[Mutations in C-terminal titin cause autosomal dominant tibial muscular dystrophy (TMD) as reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP379264.RAKVEJImpbwvfO0gu2yc_Z47GZ-dQFuRXcKgM7Hex5_k4130_provenance.
- NP522238.RAz-Z4v3cC9AT4V5LeMZYUdTblh_R3nr1AEP4U7nD7dWQ130_assertion description "[Mutations in C-terminal titin cause autosomal dominant tibial muscular dystrophy (TMD) as reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522238.RAz-Z4v3cC9AT4V5LeMZYUdTblh_R3nr1AEP4U7nD7dWQ130_provenance.
- NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_assertion description "[Mutations in C-terminal titin cause autosomal dominant tibial muscular dystrophy (TMD) as reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761405.RARPtDXHj2zgQQIuT--_hDjTo_VBKRt_st7GAhnL9tAjg130_provenance.
- NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_assertion description "[Mutations in C-terminal titin cause autosomal dominant tibial muscular dystrophy (TMD) as reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_provenance.