Matches in Nanopublications for { ?s ?p "[Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and cardiomyopathy, and genetically by mutations in the lamin A/C gene on 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_assertion description "[Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and cardiomyopathy, and genetically by mutations in the lamin A/C gene on 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214829.RAlcwFKlBpiOKlelLDiQrGJnO8ywrs7fIj7qfKMeKVwck130_provenance.
- NP729705.RABcvqSezQmziFPOPqw2RX9mwF-BG0EZSx7gDJYX4BgD8130_assertion description "[Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and cardiomyopathy, and genetically by mutations in the lamin A/C gene on 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729705.RABcvqSezQmziFPOPqw2RX9mwF-BG0EZSx7gDJYX4BgD8130_provenance.
- NP374917.RAu-x1jFSFcH0FpFtxOfLQN5InXvuox4TolFvJqSQxsgw130_assertion description "[Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and cardiomyopathy, and genetically by mutations in the lamin A/C gene on 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374917.RAu-x1jFSFcH0FpFtxOfLQN5InXvuox4TolFvJqSQxsgw130_provenance.
- NP856337.RAuCboeQq0fPKKjMaTDSu1Wc9_WAlv511nF4bq9dqJP58130_assertion description "[Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and cardiomyopathy, and genetically by mutations in the lamin A/C gene on 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856337.RAuCboeQq0fPKKjMaTDSu1Wc9_WAlv511nF4bq9dqJP58130_provenance.
- NP571381.RA3KjYuMScyzRTTXUY6s1VM7-oiBLWwNx1PPQvrS3o5ps130_assertion description "[Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and cardiomyopathy, and genetically by mutations in the lamin A/C gene on 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571381.RA3KjYuMScyzRTTXUY6s1VM7-oiBLWwNx1PPQvrS3o5ps130_provenance.
- NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_assertion description "[Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and cardiomyopathy, and genetically by mutations in the lamin A/C gene on 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_provenance.
- NP677408.RAI6aiALIV7jjWMcjpHYOJYc5rZeFC3NIkG7S9N9wnsFg130_assertion description "[Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and cardiomyopathy, and genetically by mutations in the lamin A/C gene on 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677408.RAI6aiALIV7jjWMcjpHYOJYc5rZeFC3NIkG7S9N9wnsFg130_provenance.