Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_assertion> ?p ?o ?g. }
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- NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_assertion type Assertion NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_head.
- NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_provenance.
- NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_assertion evidence source_evidence_literature NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_provenance.
- NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_assertion SIO_000772 21109227 NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_provenance.
- NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_assertion wasDerivedFrom befree-2016 NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_provenance.
- NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_assertion wasGeneratedBy ECO_0000203 NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_provenance.