Matches in Nanopublications for { ?s ?p "[X-linked hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency in an inherited disorder of purine metabolism is usually associated with the clinical manifestations of hyperuricemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[X-linked hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency in an inherited disorder of purine metabolism is usually associated with the clinical manifestations of hyperuricemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[X-linked hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency in an inherited disorder of purine metabolism is usually associated with the clinical manifestations of hyperuricemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_assertion description "[X-linked hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency in an inherited disorder of purine metabolism is usually associated with the clinical manifestations of hyperuricemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244925.RAVXe5kWJVJLgmTzXYtBoxMVi8Ymid6HUrw8rO8V8vPzk130_provenance.
- NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_assertion description "[X-linked hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency in an inherited disorder of purine metabolism is usually associated with the clinical manifestations of hyperuricemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_provenance.