Matches in Nanopublications for { ?s ?p "[Methionine adenosyltransferase I/III (MAT I/III) deficiency, caused by mutations in the MAT1A gene, is an inherited metabolic disorder characterized by persistent hypermethioninemia, usually detected by newborn mass screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_assertion description "[Methionine adenosyltransferase I/III (MAT I/III) deficiency, caused by mutations in the MAT1A gene, is an inherited metabolic disorder characterized by persistent hypermethioninemia, usually detected by newborn mass screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593985.RABKGbFqJbsqNq7BfFkuY0Xl8Gmbe37j11W_W2fphncEY130_provenance.
- NP546450.RAcXeTHnrbhHTouod5TyE_VyiSYJXAgv_qgepU-qEoC8A130_assertion description "[Methionine adenosyltransferase I/III (MAT I/III) deficiency, caused by mutations in the MAT1A gene, is an inherited metabolic disorder characterized by persistent hypermethioninemia, usually detected by newborn mass screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546450.RAcXeTHnrbhHTouod5TyE_VyiSYJXAgv_qgepU-qEoC8A130_provenance.
- NP857532.RA8Vp8XoLkJNzC-iRIFLbEmkzJs-JIQOFuNCyS0c92aDk130_assertion description "[Methionine adenosyltransferase I/III (MAT I/III) deficiency, caused by mutations in the MAT1A gene, is an inherited metabolic disorder characterized by persistent hypermethioninemia, usually detected by newborn mass screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857532.RA8Vp8XoLkJNzC-iRIFLbEmkzJs-JIQOFuNCyS0c92aDk130_provenance.
- assertion description "[Methionine adenosyltransferase I/III (MAT I/III) deficiency, caused by mutations in the MAT1A gene, is an inherited metabolic disorder characterized by persistent hypermethioninemia, usually detected by newborn mass screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1010520.RAm3r7DCtPvmvbohIEovEmniikIfZYnDZHcIJZD4skSbM130_assertion description "[Methionine adenosyltransferase I/III (MAT I/III) deficiency, caused by mutations in the MAT1A gene, is an inherited metabolic disorder characterized by persistent hypermethioninemia, usually detected by newborn mass screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010520.RAm3r7DCtPvmvbohIEovEmniikIfZYnDZHcIJZD4skSbM130_provenance.