Matches in Nanopublications for { ?s ?p "[APOPT1 mutations are responsible for infantile or childhood-onset mitochondrial disease, hallmarked by the combination of profound COX deficiency with a distinctive neuroimaging presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[APOPT1 mutations are responsible for infantile or childhood-onset mitochondrial disease, hallmarked by the combination of profound COX deficiency with a distinctive neuroimaging presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1215628.RAX1XilJKOsGHDIEwrLSpvh5xbVzwjCmybXAqOLhn2_9Y130_assertion description "[APOPT1 mutations are responsible for infantile or childhood-onset mitochondrial disease, hallmarked by the combination of profound COX deficiency with a distinctive neuroimaging presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215628.RAX1XilJKOsGHDIEwrLSpvh5xbVzwjCmybXAqOLhn2_9Y130_provenance.
- NP956004.RA1C9uvVqy97WYDKLssdsfLA8EnMELC9YRBiw3e1NZ3ew130_assertion description "[APOPT1 mutations are responsible for infantile or childhood-onset mitochondrial disease, hallmarked by the combination of profound COX deficiency with a distinctive neuroimaging presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956004.RA1C9uvVqy97WYDKLssdsfLA8EnMELC9YRBiw3e1NZ3ew130_provenance.