Matches in Nanopublications for { ?s ?p "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5840.RAa2PGeEELp3LrSpEErIaOzQM56k5tgAE2cYn5WNv0hg4130_provenance.
- assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance.
- NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834226.RAgHaBqfG728WRn3Nup91rsD3bl8uGLNETUw0WxoxKYDg130_provenance.
- NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance.
- NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance.