Matches in Nanopublications for { ?s ?p "[Calpain 3 is the muscle-specific member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_assertion description "[Calpain 3 is the muscle-specific member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_provenance.
- NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_assertion description "[Calpain 3 is the muscle-specific member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance.
- assertion description "[Calpain 3 is the muscle-specific member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Calpain 3 is the muscle-specific member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP298679.RAN7DUtczC7MQdsUrp5rPbxtnykgUlc87WWG7HRICgbdQ130_assertion description "[Calpain 3 is the muscle-specific member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298679.RAN7DUtczC7MQdsUrp5rPbxtnykgUlc87WWG7HRICgbdQ130_provenance.
- NP889720.RAz-ZBXu1CJFFe-8ri_eyPn7TE_sCJjmWzXFkvUw5iyrU130_assertion description "[Calpain 3 is the muscle-specific member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889720.RAz-ZBXu1CJFFe-8ri_eyPn7TE_sCJjmWzXFkvUw5iyrU130_provenance.
- NP298678.RA2cuT1927dF-blWFJXBGqYcZsONVp2VPy1mCydo4HWFg130_assertion description "[Calpain 3 is the muscle-specific member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298678.RA2cuT1927dF-blWFJXBGqYcZsONVp2VPy1mCydo4HWFg130_provenance.