Matches in Nanopublications for { ?s ?p "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195652.RABcbomPVLE1TTBPj5I2peXe7fV88fMVJKZp7rj2WcE5U130_provenance.
- NP301975.RA6wCzx1XXzMLVzYDve-AoEBuBynyFI2O52otRqFN_8oc130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301975.RA6wCzx1XXzMLVzYDve-AoEBuBynyFI2O52otRqFN_8oc130_provenance.
- NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461552.RA6Gg-gpFOG6S1KXI6L365G6IpuodR4ZUXSfpO8QmFDAQ130_provenance.
- NP608623.RA-BX3qSnZ8IKPhTdpvp_qYxPnlOQ2CgWQBbSr4sibY4A130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608623.RA-BX3qSnZ8IKPhTdpvp_qYxPnlOQ2CgWQBbSr4sibY4A130_provenance.
- NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779385.RA6eHm5UgBPxrUGz7wtoRMkpaeVCwi9cLGEjZ5vpI4_y8130_provenance.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782568.RAlotvGxVO00bfe5YDCIAS_rLyVoWDZUaemRZbb5RDAgw130_provenance.
- NP472593.RAvZzmWe7YWzxkNerDmPoM4OmPoJqbiG939STBrN6cI0A130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472593.RAvZzmWe7YWzxkNerDmPoM4OmPoJqbiG939STBrN6cI0A130_provenance.
- NP472594.RAjE-KBnkpiuNF6G0_HPqgC5FewnhhjTmZVp5uGjpUXqw130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472594.RAjE-KBnkpiuNF6G0_HPqgC5FewnhhjTmZVp5uGjpUXqw130_provenance.
- NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_provenance.
- NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance.