{"created":"2023-06-19T10:42:06.852235+00:00","id":1989,"links":{},"metadata":{"_buckets":{"deposit":"c0b950f1-655f-4e24-8b8f-f1598f303b68"},"_deposit":{"created_by":3,"id":"1989","owners":[3],"pid":{"revision_id":0,"type":"depid","value":"1989"},"status":"published"},"_oai":{"id":"oai:shiga-med.repo.nii.ac.jp:00001989","sets":["10:11:343"]},"author_link":["1766"],"item_2_alternative_title_18":{"attribute_name":"その他の言語のタイトル","attribute_value_mlt":[{"subitem_alternative_title":"Gilbert症候群とCrigler-Najjar症候群II型におけるビリルビンUDP-グルクロン酸転移酵素遺伝子のミスセンス変異(G71R and Y486D)の役割"},{"subitem_alternative_title":"Gilbert ショウコウグン ト Crigler Najjar ショウコウグン IIガタ ニ オケル ビリルビン UDP グルクロンサン テンイ コウソ イデンシ ノ ミスセンス ヘンイ G71R and Y486D ノ ヤクワリ"}]},"item_2_biblio_info_6":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"1998-06-30","bibliographicIssueDateType":"Issued"},"bibliographic_titles":[{}]}]},"item_2_description_42":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"subitem_description":"Others","subitem_description_type":"Other"}]},"item_2_description_5":{"attribute_name":"内容記述","attribute_value_mlt":[{"subitem_description":"学位授与機関：　滋賀医科大学　博士（医学）（論）第239号　平成10年6月30日","subitem_description_type":"Other"},{"subitem_description":"Biochimica et Biophysica Acta. 1998, 1406(3), p.267-273.","subitem_description_type":"Other"}]},"item_2_publisher_32":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"滋賀医科大学"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"山本, 和雄"}],"nameIdentifiers":[{},{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2017-02-16"}],"displaytype":"detail","filename":"hr239.pdf","filesize":[{"value":"2.0 MB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"hr239.pdf","url":"https://shiga-med.repo.nii.ac.jp/record/1989/files/hr239.pdf"},"version_id":"7f40d095-367a-4ceb-9001-c5c5f93b9178"}]},"item_language":{"attribute_name":"言語","attribute_value_mlt":[{"subitem_language":"jpn"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"other","resourceuri":"http://purl.org/coar/resource_type/c_1843"}]},"item_title":"Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II.","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II."}]},"item_type_id":"2","owner":"3","path":["343"],"pubdate":{"attribute_name":"公開日","attribute_value":"2014-11-13"},"publish_date":"2014-11-13","publish_status":"0","recid":"1989","relation_version_is_last":true,"title":["Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II."],"weko_creator_id":"3","weko_shared_id":3},"updated":"2023-06-19T11:50:24.964120+00:00"}