Matches in Nanopublications for { ?s ?p "[The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or symptoms of skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP881215.RAVqwPJF5r9__IB_r8hKgGFb3B_uoNAXskDppKXzZu89M130_assertion description "[The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or symptoms of skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881215.RAVqwPJF5r9__IB_r8hKgGFb3B_uoNAXskDppKXzZu89M130_provenance.
- NP831455.RAs_32A655vqIyMY5ht-mF_jBhWx43N8pXBo9P24j0uW4130_assertion description "[The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or symptoms of skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831455.RAs_32A655vqIyMY5ht-mF_jBhWx43N8pXBo9P24j0uW4130_provenance.
- NP583308.RA2rdsEgEzNDoeb3oRRnu5Hv5P50DCuC3DL0c5tgLCeHA130_assertion description "[The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or symptoms of skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583308.RA2rdsEgEzNDoeb3oRRnu5Hv5P50DCuC3DL0c5tgLCeHA130_provenance.
- NP583414.RAzyYs9OcRaVbG_XlMRGRyMNl0bPpJma_OyX7c91wg_mk130_assertion description "[The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or symptoms of skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583414.RAzyYs9OcRaVbG_XlMRGRyMNl0bPpJma_OyX7c91wg_mk130_provenance.
- NP604540.RAVCXyH2PfUJl-LjHNLpVEpjtFlbFos1idXXEeOF2qyzE130_assertion description "[The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or symptoms of skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604540.RAVCXyH2PfUJl-LjHNLpVEpjtFlbFos1idXXEeOF2qyzE130_provenance.
- NP604543.RAV_eYeDJdatnde1d6MLidg5j8K_vPN4mshPSW0cZqnu4130_assertion description "[The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or symptoms of skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604543.RAV_eYeDJdatnde1d6MLidg5j8K_vPN4mshPSW0cZqnu4130_provenance.
- assertion description "[The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or symptoms of skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or symptoms of skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.