Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_assertion type Assertion NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_head.
- NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_assertion description "[The severe neonatal X-linked form (myotubular myopathy) is due to mutations in the phosphoinositide phosphatase myotubularin (MTM1), whereas mutations in dynamin 2 (DNM2) have been found in some autosomal dominant cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance.
- NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_assertion evidence source_evidence_literature NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance.
- NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_assertion SIO_000772 17676042 NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance.
- NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_assertion wasDerivedFrom befree-2016 NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance.
- NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_assertion wasGeneratedBy ECO_0000203 NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance.