Matches in Nanopublications for { ?s ?p "[in a kindred with a syndrome including hypertension, hypercholesterolemia & hypomagnesemia, analysis of maternal lineage mitochondrial genome identified a mutation substituting cytidine for uridine immediately 5'to the mitochondrial TRNA (Ile) anticodon ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_assertion description "[in a kindred with a syndrome including hypertension, hypercholesterolemia & hypomagnesemia, analysis of maternal lineage mitochondrial genome identified a mutation substituting cytidine for uridine immediately 5'to the mitochondrial TRNA (Ile) anticodon ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_provenance.
- NP123421.RA1GXOUKzZDsywBrq_YJwWur9dD7UHYmLG7AQ349uh3Ig130_assertion description "[in a kindred with a syndrome including hypertension, hypercholesterolemia & hypomagnesemia, analysis of maternal lineage mitochondrial genome identified a mutation substituting cytidine for uridine immediately 5'to the mitochondrial TRNA (Ile) anticodon ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123421.RA1GXOUKzZDsywBrq_YJwWur9dD7UHYmLG7AQ349uh3Ig130_provenance.
- NP207443.RAKcSvTFePs9SS6GeHUD7CLPpVJhWCUPtsrr08ned-UTA130_assertion description "[in a kindred with a syndrome including hypertension, hypercholesterolemia & hypomagnesemia, analysis of maternal lineage mitochondrial genome identified a mutation substituting cytidine for uridine immediately 5'to the mitochondrial TRNA (Ile) anticodon ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207443.RAKcSvTFePs9SS6GeHUD7CLPpVJhWCUPtsrr08ned-UTA130_provenance.
- NP207444.RAyDzhCoel59066zHowO3uyS1woz_4xoRb2GJl5NZ8bIU130_assertion description "[in a kindred with a syndrome including hypertension, hypercholesterolemia & hypomagnesemia, analysis of maternal lineage mitochondrial genome identified a mutation substituting cytidine for uridine immediately 5'to the mitochondrial TRNA (Ile) anticodon ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207444.RAyDzhCoel59066zHowO3uyS1woz_4xoRb2GJl5NZ8bIU130_provenance.