Matches in Nanopublications for { ?s ?p "[Myotonic dystrophy type 1 (DM1) is a multi-systemic disorder caused by a CTG trinucleotide repeat expansion (CTG(exp)) in the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_assertion description "[Myotonic dystrophy type 1 (DM1) is a multi-systemic disorder caused by a CTG trinucleotide repeat expansion (CTG(exp)) in the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693486.RAXniJramJ3reVNx_yjBgpuOnr0x3GWb7_YNwYE1pLD_s130_provenance.
- NP766214.RAqU44sTXbBrlQ7hmRngqAtBD0U5AuvwHubOZhpMMK1Mg130_assertion description "[Myotonic dystrophy type 1 (DM1) is a multi-systemic disorder caused by a CTG trinucleotide repeat expansion (CTG(exp)) in the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766214.RAqU44sTXbBrlQ7hmRngqAtBD0U5AuvwHubOZhpMMK1Mg130_provenance.
- assertion description "[Myotonic dystrophy type 1 (DM1) is a multi-systemic disorder caused by a CTG trinucleotide repeat expansion (CTG(exp)) in the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP968692.RA1iduU-2jnbaP0b0vc23GvliL5zd9R751FmAMa1i0XtM130_assertion description "[Myotonic dystrophy type 1 (DM1) is a multi-systemic disorder caused by a CTG trinucleotide repeat expansion (CTG(exp)) in the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968692.RA1iduU-2jnbaP0b0vc23GvliL5zd9R751FmAMa1i0XtM130_provenance.
- NP968691.RAOReakMGryK8V5mWbR-cZtThEcjuTfZpIlCyTRbp-BLE130_assertion description "[Myotonic dystrophy type 1 (DM1) is a multi-systemic disorder caused by a CTG trinucleotide repeat expansion (CTG(exp)) in the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968691.RAOReakMGryK8V5mWbR-cZtThEcjuTfZpIlCyTRbp-BLE130_provenance.