Matches in Nanopublications for { ?s ?p "[Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1184268.RAItrC09cRsODsb97m-O9P5fgTQBZ90SAz_TXqJ2fv1pQ130_assertion description "[Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184268.RAItrC09cRsODsb97m-O9P5fgTQBZ90SAz_TXqJ2fv1pQ130_provenance.
- NP1184267.RA4uAg9DQyOVgtS8OWJVqAe3X8meZn0oPnJ0gKN2x7yvI130_assertion description "[Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184267.RA4uAg9DQyOVgtS8OWJVqAe3X8meZn0oPnJ0gKN2x7yvI130_provenance.