Matches in Nanopublications for { ?s ?p "[Lesch-Nyhan disease (LND) is a rare X-linked recessive genetic disorder caused by a deficiency of hypoxanthine-guanine phosphoribosyltransferase (HPRT) enzyme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Lesch-Nyhan disease (LND) is a rare X-linked recessive genetic disorder caused by a deficiency of hypoxanthine-guanine phosphoribosyltransferase (HPRT) enzyme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_assertion description "[Lesch-Nyhan disease (LND) is a rare X-linked recessive genetic disorder caused by a deficiency of hypoxanthine-guanine phosphoribosyltransferase (HPRT) enzyme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804508.RAh9slNjpbYbXfZHGgGxDVSiYw2sM98LEwJnaMJgUmAXg130_provenance.
- NP558778.RAAEOPjeHYHYT_GufpcebgaX1l1IDDjBX_czM8Qcd3JgI130_assertion description "[Lesch-Nyhan disease (LND) is a rare X-linked recessive genetic disorder caused by a deficiency of hypoxanthine-guanine phosphoribosyltransferase (HPRT) enzyme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558778.RAAEOPjeHYHYT_GufpcebgaX1l1IDDjBX_czM8Qcd3JgI130_provenance.