Matches in Nanopublications for { ?s ?p "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_provenance.
- NP802831.RAsLp7jyatZLjV6-nIgF6L4UI6ZRUd6OAYnduLuQySPEE130_assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802831.RAsLp7jyatZLjV6-nIgF6L4UI6ZRUd6OAYnduLuQySPEE130_provenance.
- NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_provenance.
- NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance.
- NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_provenance.
- NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_provenance.