Matches in Nanopublications for { ?s ?p "[We recently characterized the mitochondrial ornithine transporter (ORNT1), the gene defective in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome, a urea cycle disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_assertion description "[We recently characterized the mitochondrial ornithine transporter (ORNT1), the gene defective in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome, a urea cycle disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP517872.RAa60w6DVm_29YI7nYLu-hp3cakCubuyu6uTbiJwTFX98130_provenance.
- NP875107.RAwlf-822oouE-dbV1Xohlr5HWStzfPtE6oBA-qHG1iZ4130_assertion description "[We recently characterized the mitochondrial ornithine transporter (ORNT1), the gene defective in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome, a urea cycle disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875107.RAwlf-822oouE-dbV1Xohlr5HWStzfPtE6oBA-qHG1iZ4130_provenance.