Matches in Nanopublications for { ?s ?p "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP721790.RAY9YQtY6tGhKWWVg-BkaOqVr2_WIDXAm1x3x8dJoDKZ4130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP721790.RAY9YQtY6tGhKWWVg-BkaOqVr2_WIDXAm1x3x8dJoDKZ4130_provenance.
- NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance.
- NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698478.RAgwhs0CouNUUexbN96ANt7S9nxWcaAG9GSsvaQYHemt4130_provenance.
- NP966876.RAB7yTXEStJq71IXnraHI7xcz0Nv9QxoiYOOP8ZKZWLiQ130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966876.RAB7yTXEStJq71IXnraHI7xcz0Nv9QxoiYOOP8ZKZWLiQ130_provenance.
- NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance.
- NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_provenance.
- NP966878.RA4aU3MoTLtILx1T3jM0ttmKnn02BIereicax7DZuBv6g130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966878.RA4aU3MoTLtILx1T3jM0ttmKnn02BIereicax7DZuBv6g130_provenance.
- NP782526.RAHWvY7ky9h-De4NrcyT_MwoLtoU3-67acpfqxgyQw1NA130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782526.RAHWvY7ky9h-De4NrcyT_MwoLtoU3-67acpfqxgyQw1NA130_provenance.
- NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance.
- assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.