Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP835034.RAPawFJFhoFC_vtspqa9gbmS0goYEdD9rY40UpESFlnUg#assertion> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion wasGeneratedBy ECO_0000203 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion SIO_000772 25430934 provenance.
- assertion evidence source_evidence_literature provenance.
- assertion description "[The most common CMT subtypes were CMT1A/PMP22 duplication, CMT1X/GJB1 mutation, CMT2A/MFN2 mutation, CMT1B/MPZ mutation, and hereditary neuropathy with liability to pressure palsy/PMP22 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.