Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_assertion> ?p ?o ?g. }
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- NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_assertion type Assertion NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_head.
- NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_assertion description "[Mutations in the lamin A/C gene should be sought in any infant with dystrophic features and normal tissue immunochemical studies; especially in the presence of moderately elevated serum creatine kinase, predominant axial and humeroperoneal weakness, spine rigidity, and joint contractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_provenance.
- NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_assertion evidence source_evidence_literature NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_provenance.
- NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_assertion SIO_000772 20837309 NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_provenance.
- NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_assertion wasDerivedFrom befree-20150227 NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_provenance.
- NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_assertion wasGeneratedBy ECO_0000203 NP537917.RAAjiMLbVj9fDs9W_-u8usLIudkfa4iTRa1wTolXoYeVg130_provenance.