Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_assertion> ?p ?o ?g. }
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- NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_assertion type Assertion NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_head.
- 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.
- NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_assertion evidence source_evidence_literature NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_provenance.
- NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_assertion SIO_000772 7573046 NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_provenance.
- NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_assertion wasDerivedFrom befree-2016 NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_provenance.
- NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_assertion wasGeneratedBy ECO_0000203 NP1313003.RANNFNVnnGR6XKs5ieeH1cjmNlgs3tC91XJfxaTUk3prM130_provenance.