Matches in Nanopublications for { ?s ?p "[Myotonic dystrophy type 2 (DM2) is an autosomal dominant inherited disorder with (CCTG)n repeat 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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- assertion description "[Myotonic dystrophy type 2 (DM2) is an autosomal dominant inherited disorder with (CCTG)n repeat expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1216579.RAsqnZN6UR9Yz8HhKfNM5lAan95wqrPND0CRp3JVk_ULs130_assertion description "[Myotonic dystrophy type 2 (DM2) is an autosomal dominant inherited disorder with (CCTG)n repeat expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216579.RAsqnZN6UR9Yz8HhKfNM5lAan95wqrPND0CRp3JVk_ULs130_provenance.
- NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_assertion description "[Myotonic dystrophy type 2 (DM2) is an autosomal dominant inherited disorder with (CCTG)n repeat expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_provenance.
- NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_assertion description "[Myotonic dystrophy type 2 (DM2) is an autosomal dominant inherited disorder with (CCTG)n repeat expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance.