Matches in Nanopublications for { ?s ?p "[Duchenne muscular dystrophy (DMD) is an inherited muscle-wasting disease caused by the absence of a muscle cytoskeletal protein, dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP672447.RAa2YqqnBdEfYdFzFM0MBdz1UU1rRXiPwng0FRBJ_LbJc130_assertion description "[Duchenne muscular dystrophy (DMD) is an inherited muscle-wasting disease caused by the absence of a muscle cytoskeletal protein, dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672447.RAa2YqqnBdEfYdFzFM0MBdz1UU1rRXiPwng0FRBJ_LbJc130_provenance.
- NP878463.RASVToS4vylZdmKDBIGG9Rz_oT8XCl8jvv1RiqgXWFypg130_assertion description "[Duchenne muscular dystrophy (DMD) is an inherited muscle-wasting disease caused by the absence of a muscle cytoskeletal protein, dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP878463.RASVToS4vylZdmKDBIGG9Rz_oT8XCl8jvv1RiqgXWFypg130_provenance.
- assertion description "[Duchenne muscular dystrophy (DMD) is an inherited muscle-wasting disease caused by the absence of a muscle cytoskeletal protein, dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP357049.RAdXaBd_2jmfhLHZlVqdBK99OLWR_1aqHhowsZzfbZJcI130_assertion description "[Duchenne muscular dystrophy (DMD) is an inherited muscle-wasting disease caused by the absence of a muscle cytoskeletal protein, dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357049.RAdXaBd_2jmfhLHZlVqdBK99OLWR_1aqHhowsZzfbZJcI130_provenance.
- NP268154.RACXYB4WFkIZfdRGwVxesCNTIXRBa-wzjimVHLjgliTGA130_assertion description "[Duchenne muscular dystrophy (DMD) is an inherited muscle-wasting disease caused by the absence of a muscle cytoskeletal protein, dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268154.RACXYB4WFkIZfdRGwVxesCNTIXRBa-wzjimVHLjgliTGA130_provenance.