Matches in Nanopublications for { ?s ?p "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion description "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
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- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion description "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
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- NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_assertion description "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_provenance.