Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_assertion> ?p ?o ?g. }
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- NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_assertion type Assertion NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_head.
- NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_assertion description "[Dysferlin deficiency in muscle is the most relevant feature for the diagnosis of dysferlinopathy and prompts the search for mutations in DYSF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_provenance.
- NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_assertion evidence source_evidence_literature NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_provenance.
- NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_assertion SIO_000772 16010686 NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_provenance.
- NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_assertion wasDerivedFrom befree-2016 NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_provenance.
- NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_assertion wasGeneratedBy ECO_0000203 NP503632.RArJ5mqZGLVZmKQHaQwu--J6gYBOUYaND_8TiFMfjNCUo130_provenance.