Matches in Nanopublications for { ?s ?p "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP248540.RA4WdxOL7MiRKfDjW0iVaOx9N2g2HVpoG5UdNtjUnclFQ130_assertion description "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248540.RA4WdxOL7MiRKfDjW0iVaOx9N2g2HVpoG5UdNtjUnclFQ130_provenance.
- NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_assertion description "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354206.RA6LyEaxPtyAwVH7UnCxxURK-ddic9if1Vyn8B86Oy99U130_provenance.
- NP702973.RArtJbQ6JrZABBgI99x9tj013GK7B9Dxh2-a9waAZi3Vo130_assertion description "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702973.RArtJbQ6JrZABBgI99x9tj013GK7B9Dxh2-a9waAZi3Vo130_provenance.
- NP791594.RAUJoU-OQU8MpHmNGVwwYZ1bkHvPhQSff2Jd-UfEvEftw130_assertion description "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791594.RAUJoU-OQU8MpHmNGVwwYZ1bkHvPhQSff2Jd-UfEvEftw130_provenance.
- NP721240.RA1WuePwU_k_6wdIF5p_vJwj9sFkUgTNyqwJDO6Fv1txE130_assertion description "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP721240.RA1WuePwU_k_6wdIF5p_vJwj9sFkUgTNyqwJDO6Fv1txE130_provenance.
- NP666936.RAxmRq_5d6rDs_q95xbqnI-sNaV2BG2vccxI7SGzmlM5M130_assertion description "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666936.RAxmRq_5d6rDs_q95xbqnI-sNaV2BG2vccxI7SGzmlM5M130_provenance.
- NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_assertion description "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_provenance.
- NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_assertion description "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_provenance.