Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_assertion> ?p ?o ?g. }
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- NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_assertion type Assertion NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_head.
- 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.
- NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_assertion evidence source_evidence_literature NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_provenance.
- NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_assertion SIO_000772 25648254 NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_provenance.
- NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_assertion wasDerivedFrom befree-2016 NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_provenance.
- NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_assertion wasGeneratedBy ECO_0000203 NP1260758.RAhfiuDlHV69wBu3JSaADnOjKaKz1exSObKY0wCHuhC80130_provenance.