Matches in Nanopublications for { ?s ?p "[Missense mutations of ACTA1 cause an autosomal dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_assertion description "[Missense mutations of ACTA1 cause an autosomal dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance.
- assertion description "[Missense mutations of ACTA1 cause an autosomal dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion description "[Missense mutations of ACTA1 cause an autosomal dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_assertion description "[Missense mutations of ACTA1 cause an autosomal dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_provenance.