{"created":"2021-03-01T06:10:59.170613+00:00","id":7137,"links":{},"metadata":{"_buckets":{"deposit":"364a590a-a24d-48d9-8595-cbe09e4245cb"},"_deposit":{"id":"7137","owners":[],"pid":{"revision_id":0,"type":"depid","value":"7137"},"status":"published"},"_oai":{"id":"oai:soar-ir.repo.nii.ac.jp:00007137","sets":["461:848:849"]},"author_link":["17230"],"item_14_biblio_info_6":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2014-03-26","bibliographicIssueDateType":"Issued"}}]},"item_14_date_granted_8":{"attribute_name":"学位授与年月日","attribute_value_mlt":[{"subitem_dategranted":"2014-03-26"}]},"item_14_degree_grantor_10":{"attribute_name":"学位授与機関","attribute_value_mlt":[{"subitem_degreegrantor":[{"subitem_degreegrantor_name":"信州大学(Shinshu university)"}],"subitem_degreegrantor_identifier":[{"subitem_degreegrantor_identifier_name":"13601","subitem_degreegrantor_identifier_scheme":"kakenhi"}]}]},"item_14_degree_name_9":{"attribute_name":"学位名","attribute_value_mlt":[{"subitem_degreename":"博士(医学)"}]},"item_14_description_26":{"attribute_name":"内容記述","attribute_value_mlt":[{"subitem_description":"雑誌に発表。JOURNAL OF HUMAN GENETICS. 59(2):100-106 (2014); doi:10.1038/jhg.2013.128.","subitem_description_type":"Other"}]},"item_14_description_37":{"attribute_name":"資源タイプ(コンテンツの種類)","attribute_value_mlt":[{"subitem_description":"Thesis","subitem_description_type":"Other"}]},"item_14_description_5":{"attribute_name":"引用","attribute_value_mlt":[{"subitem_description":"矢野 卓也. Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening(非症候群性難聴患者における難聴関連遺伝子変異について:全ミトコンドリア遺伝子スクリーニングを用いた検討). 信州大学, 2014, 博士論文.","subitem_description_type":"Other"}]},"item_14_dissertation_number_7":{"attribute_name":"学位授与番号","attribute_value_mlt":[{"subitem_dissertationnumber":"13601乙第1176号"}]},"item_14_publisher_4":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"信州大学"}]},"item_14_relation_54":{"attribute_name":"PubMed","attribute_value_mlt":[{"subitem_relation_name":[{"subitem_relation_name_text":"24401907"}],"subitem_relation_type_id":{"subitem_relation_type_id_text":"https://pubmed.ncbi.nlm.nih.gov/24401907/","subitem_relation_type_select":"PMID"}}]},"item_14_relation_55":{"attribute_name":"DOI","attribute_value_mlt":[{"subitem_relation_name":[{"subitem_relation_name_text":"10.1038/jhg.2013.128"}],"subitem_relation_type_id":{"subitem_relation_type_id_text":"https://doi.org/10.1038/jhg.2013.128","subitem_relation_type_select":"DOI"}}]},"item_14_rights_69":{"attribute_name":"権利","attribute_value_mlt":[{"subitem_rights":"Copyright © 2014 The Japan Society of Human Genetics All rights reserved 1434-5161/14"}]},"item_14_text_11":{"attribute_name":"学位の区分","attribute_value_mlt":[{"subitem_text_value":"doctoral"}]},"item_14_text_12":{"attribute_name":"学位の分野","attribute_value_mlt":[{"subitem_text_value":"医学"}]},"item_14_text_13":{"attribute_name":"学位の報告番号","attribute_value_mlt":[{"subitem_text_value":"乙第1176号"}]},"item_1627890986942":{"attribute_name":"出版タイプ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_be7fb7dd8ff6fe43","subitem_version_type":"NA"}]},"item_access_right":{"attribute_name":"アクセス権","attribute_value_mlt":[{"subitem_access_right":"open access","subitem_access_right_uri":"http://purl.org/coar/access_right/c_abf2"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"矢野, 卓也","creatorNameLang":"ja"}],"nameIdentifiers":[{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2015-09-25"}],"displaytype":"detail","filename":"13MR0012_yoshi.pdf","filesize":[{"value":"178.6 kB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"内容の要旨","url":"https://soar-ir.repo.nii.ac.jp/record/7137/files/13MR0012_yoshi.pdf"},"version_id":"2a45bc61-14f8-4103-8e8d-bef6d958fa57"},{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2015-09-25"}],"displaytype":"detail","filename":"13MR0012_shinsa.pdf","filesize":[{"value":"142.6 kB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"審査結果の要旨","url":"https://soar-ir.repo.nii.ac.jp/record/7137/files/13MR0012_shinsa.pdf"},"version_id":"1e3702be-ff41-4da4-9e62-c28256fd6f07"},{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2015-09-25"}],"displaytype":"detail","filename":"13MR0012_ronbun.pdf","filesize":[{"value":"848.3 kB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"博士論文の全文","objectType":"fulltext","url":"https://soar-ir.repo.nii.ac.jp/record/7137/files/13MR0012_ronbun.pdf"},"version_id":"2a0f4631-f77f-4219-bbc3-c6e46bb5af5c"}]},"item_language":{"attribute_name":"言語","attribute_value_mlt":[{"subitem_language":"eng"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"doctoral thesis","resourceuri":"http://purl.org/coar/resource_type/c_db06"}]},"item_title":"Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening(非症候群性難聴患者における難聴関連遺伝子変異について:全ミトコンドリア遺伝子スクリーニングを用いた検討)","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening(非症候群性難聴患者における難聴関連遺伝子変異について:全ミトコンドリア遺伝子スクリーニングを用いた検討)","subitem_title_language":"en"}]},"item_type_id":"14","owner":"1","path":["849"],"pubdate":{"attribute_name":"PubDate","attribute_value":"2014-11-27"},"publish_date":"2014-11-27","publish_status":"0","recid":"7137","relation_version_is_last":true,"title":["Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening(非症候群性難聴患者における難聴関連遺伝子変異について:全ミトコンドリア遺伝子スクリーニングを用いた検討)"],"weko_creator_id":"1","weko_shared_id":-1},"updated":"2023-04-14T05:05:14.304034+00:00"}