Matches in Nanopublications for { ?s ?p "[Except the PMP22 duplication, disease causing CNVs are rare but may cause CMT in about 1% (95% CI 0-7%) of the Norwegian CMT families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Except the PMP22 duplication, disease causing CNVs are rare but may cause CMT in about 1% (95% CI 0-7%) of the Norwegian CMT families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_assertion description "[Except the PMP22 duplication, disease causing CNVs are rare but may cause CMT in about 1% (95% CI 0-7%) of the Norwegian CMT families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_provenance.
- NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_assertion description "[Except the PMP22 duplication, disease causing CNVs are rare but may cause CMT in about 1% (95% CI 0-7%) of the Norwegian CMT families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_provenance.