Matches in Nanopublications for { ?s ?p "[Recently, SIMPLE/LITAF was shown to be responsible for an autosomal dominant demyelinating form of CMT linked to 16p (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_assertion description "[Recently, SIMPLE/LITAF was shown to be responsible for an autosomal dominant demyelinating form of CMT linked to 16p (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3800.RAXdBjNvP-y0H7mgadHOvAA4w1d0OpNFCsSdVbNO1YY9Q130_provenance.
- NP4504.RA9gtm-M5K66gW9uXeobWlkPkGDl34bdYV5MUITc9oYG4130_assertion description "[Recently, SIMPLE/LITAF was shown to be responsible for an autosomal dominant demyelinating form of CMT linked to 16p (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4504.RA9gtm-M5K66gW9uXeobWlkPkGDl34bdYV5MUITc9oYG4130_provenance.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion description "[Recently, SIMPLE/LITAF was shown to be responsible for an autosomal dominant demyelinating form of CMT linked to 16p (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_assertion description "[Recently, SIMPLE/LITAF was shown to be responsible for an autosomal dominant demyelinating form of CMT linked to 16p (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance.
- assertion description "[Recently, SIMPLE/LITAF was shown to be responsible for an autosomal dominant demyelinating form of CMT linked to 16p (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.