Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP623588.RAk_l6onUxn6ZRruoxUoI_hbOOHUymGQVaxcMQcYbQ8Fw130_provenance.