Matches in Nanopublications for { ?s ?p "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP278086.RAqOWwkU1EW0gNMGzoSMtWilpQhSGGunxKarT9m2FmaSA130_assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278086.RAqOWwkU1EW0gNMGzoSMtWilpQhSGGunxKarT9m2FmaSA130_provenance.
- assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_provenance.
- NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_provenance.
- NP620388.RAegvKXnGx1CZKj-CpHN4ale8JRzYcKtsynBRGa8D6Czk130_assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620388.RAegvKXnGx1CZKj-CpHN4ale8JRzYcKtsynBRGa8D6Czk130_provenance.
- NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_provenance.
- NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620387.RAEEucCEStYaj80sVzf5hmteAjC457MZSULc6fMmRIghQ130_provenance.