Matches in Nanopublications for { ?s ?p "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_assertion description "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_provenance.
- NP565518.RAjmhJGf0cXWM19oM5JBdJYYJ4um1MtPg2_pUG50HVsYM130_assertion description "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565518.RAjmhJGf0cXWM19oM5JBdJYYJ4um1MtPg2_pUG50HVsYM130_provenance.
- NP827247.RAd4aDiL2VI2DlkOPqSJyUFOaufzbFBPzunWgwEfu061Q130_assertion description "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827247.RAd4aDiL2VI2DlkOPqSJyUFOaufzbFBPzunWgwEfu061Q130_provenance.
- assertion description "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP868137.RAn0MS0DWA7JcsExwB84RfP1MAztNS85NMyygECpKX9yM130_assertion description "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868137.RAn0MS0DWA7JcsExwB84RfP1MAztNS85NMyygECpKX9yM130_provenance.
- NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_assertion description "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_provenance.
- NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_assertion description "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313004.RANsCU3dRbhj52DHm_mRIlPk5Yp_qz4nRwrsYtUa2u6n0130_provenance.