Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_assertion> ?p ?o ?g. }
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- NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_assertion type Assertion NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_head.
- NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_assertion description "[Charcot-Marie-Tooth disease (CMT) and related inherited peripheral neuropathies, including Dejerine-Sottas syndrome, congenital hypomyelination, and hereditary neuropathy with liability to pressure palsies (HNPP), are caused by mutations in three myelin genes: PMP22, MPZ and Cx32 (GJB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_provenance.
- NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_assertion evidence source_evidence_literature NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_provenance.
- NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_assertion SIO_000772 10737979 NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_provenance.
- NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_assertion wasDerivedFrom befree-2016 NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_provenance.
- NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_assertion wasGeneratedBy ECO_0000203 NP279264.RAAtLwDn-VwglEFcGYjdqxjzb-UIz36IzZLByPKcAYCkU130_provenance.