Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_assertion> ?p ?o ?g. }
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- NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_assertion type Assertion NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_head.
- NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_assertion description "[Recently, mutations in the ubiquitously expressed dynamin 2 (dyn2) protein were found in patients with Charcot-Marie-Tooth (CMT) disease, which is an inherited peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_provenance.
- NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_assertion evidence source_evidence_literature NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_provenance.
- NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_assertion SIO_000772 19528294 NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_provenance.
- NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_assertion wasDerivedFrom befree-20140225 NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_provenance.
- NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_assertion wasGeneratedBy ECO_0000203 NP237894.RAaCEL5p9WP7W2oBUvb1tdTD_sfgrCbvpLQhEfNeXUbNQ130_provenance.