Matches in Nanopublications for { ?s ?p "[Sequence analysis of the UGT1A1 gene revealed that she was a compound heterozygote with p.[G71R; Y486D] + [Y486D] mutations, which suggests Crigler-Najjar syndrome type II rather than GS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- NP919992.RA_-xSGKtNtIfa3yK-viaSl3YPCSZxF96aAUSMt-_KQ0A130_assertion description "[Sequence analysis of the UGT1A1 gene revealed that she was a compound heterozygote with p.[G71R; Y486D] + [Y486D] mutations, which suggests Crigler-Najjar syndrome type II rather than GS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919992.RA_-xSGKtNtIfa3yK-viaSl3YPCSZxF96aAUSMt-_KQ0A130_provenance.
- NP872268.RABcnjYdJY-xSgYxPHvufWXeKPY2Iwj7Xj6oNaotCfk7Q130_assertion description "[Sequence analysis of the UGT1A1 gene revealed that she was a compound heterozygote with p.[G71R; Y486D] + [Y486D] mutations, which suggests Crigler-Najjar syndrome type II rather than GS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872268.RABcnjYdJY-xSgYxPHvufWXeKPY2Iwj7Xj6oNaotCfk7Q130_provenance.
- NP913115.RA9kh5ziZZ8TpwQ9e11N11hYmeLLOLswXBMv96au0GoxM130_assertion description "[Sequence analysis of the UGT1A1 gene revealed that she was a compound heterozygote with p.[G71R; Y486D] + [Y486D] mutations, which suggests Crigler-Najjar syndrome type II rather than GS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913115.RA9kh5ziZZ8TpwQ9e11N11hYmeLLOLswXBMv96au0GoxM130_provenance.
- assertion description "[Sequence analysis of the UGT1A1 gene revealed that she was a compound heterozygote with p.[G71R; Y486D] + [Y486D] mutations, which suggests Crigler-Najjar syndrome type II rather than GS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Sequence analysis of the UGT1A1 gene revealed that she was a compound heterozygote with p.[G71R; Y486D] + [Y486D] mutations, which suggests Crigler-Najjar syndrome type II rather than GS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.