Matches in Nanopublications for { ?s ?p "[Congenital myotonic dystrophy (CDM1) and myotonic dystrophy of type 1 (DM1) or of type 2 (DM2) are caused by the expression of mutant RNAs containing expanded CUG or CCUG repeats, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_assertion description "[Congenital myotonic dystrophy (CDM1) and myotonic dystrophy of type 1 (DM1) or of type 2 (DM2) are caused by the expression of mutant RNAs containing expanded CUG or CCUG repeats, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_provenance.
- NP569671.RAmccmsC12XP0adWO-EeFdWVmgGpCRf_r1EinweOQn4To130_assertion description "[Congenital myotonic dystrophy (CDM1) and myotonic dystrophy of type 1 (DM1) or of type 2 (DM2) are caused by the expression of mutant RNAs containing expanded CUG or CCUG repeats, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569671.RAmccmsC12XP0adWO-EeFdWVmgGpCRf_r1EinweOQn4To130_provenance.
- NP755599.RAU6F40-PGt2JTgw9d9_ObrNZBTGE-xFE5tTFG4RotsJM130_assertion description "[Congenital myotonic dystrophy (CDM1) and myotonic dystrophy of type 1 (DM1) or of type 2 (DM2) are caused by the expression of mutant RNAs containing expanded CUG or CCUG repeats, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755599.RAU6F40-PGt2JTgw9d9_ObrNZBTGE-xFE5tTFG4RotsJM130_provenance.
- NP242515.RA_D0haki6Svbn-t-UzV68jDjWwAFYR9655GfN7RnoYWA130_assertion description "[Congenital myotonic dystrophy (CDM1) and myotonic dystrophy of type 1 (DM1) or of type 2 (DM2) are caused by the expression of mutant RNAs containing expanded CUG or CCUG repeats, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP242515.RA_D0haki6Svbn-t-UzV68jDjWwAFYR9655GfN7RnoYWA130_provenance.
- NP625099.RAPr6GA2LktBNetSJMAePmjxVzuh5DAEoZXJKQGCuliBk130_assertion description "[Congenital myotonic dystrophy (CDM1) and myotonic dystrophy of type 1 (DM1) or of type 2 (DM2) are caused by the expression of mutant RNAs containing expanded CUG or CCUG repeats, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625099.RAPr6GA2LktBNetSJMAePmjxVzuh5DAEoZXJKQGCuliBk130_provenance.