Matches in Nanopublications for { ?s ?p "[The autosomal recessive disorder primary hyperoxaluria type 1 (PH1) is caused by a deficiency of the liver-specific pyridoxal-phosphate-dependent enzyme alanine:glyoxylate aminotransferase (AGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP256.RAmcYk4SbZ1DA8qPoA0GDt2fAJSs9y0P6JniEo7TOsqms130_assertion description "[The autosomal recessive disorder primary hyperoxaluria type 1 (PH1) is caused by a deficiency of the liver-specific pyridoxal-phosphate-dependent enzyme alanine:glyoxylate aminotransferase (AGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256.RAmcYk4SbZ1DA8qPoA0GDt2fAJSs9y0P6JniEo7TOsqms130_provenance.