{"_buckets": {"deposit": "de3db284-2e41-4096-86b5-e0a6432842d6"}, "_deposit": {"id": "22874", "owners": [], "pid": {"revision_id": 0, "type": "depid", "value": "22874"}, "status": "published"}, "_oai": {"id": "oai:niigata-u.repo.nii.ac.jp:00022874", "sets": ["456", "1209"]}, "item_7_alternative_title_1": {"attribute_name": "その他のタイトル", "attribute_value_mlt": [{"subitem_alternative_title": "DNA Diagnosis of Hemophilias(Molecular Genetic Approaches to Human Diseases)"}]}, "item_7_biblio_info_6": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "1989-06", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "6", "bibliographicPageEnd": "461", "bibliographicPageStart": "457", "bibliographicVolumeNumber": "103", "bibliographic_titles": [{"bibliographic_title": "新潟医学会雑誌"}, {"bibliographic_title": "新潟医学会雑誌", "bibliographic_titleLang": "en"}]}]}, "item_7_description_4": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "Hemophilias A and B are the most common hereditary hemorrhagic disorders that are caused by a deficiency or dysfunction of coagulation factors VIII and IX, respectively. Recently, both the factor VIII and the factor IX genes have been cloned and well characterized, and three and five intragenic RFLPs (restriction fragment length polymorphisms) of the factor VIII and the factor IX genes, respectively, have been identified. These RFLPs can be successfully used for prenatal diagnosis and carrier detection of hemophilia A. DNA diagnosis of hemophilia B in Japanese, however, is not successful due to the absence of common polymorphisms thus far identified in Caucasians.", "subitem_description_type": "Abstract"}]}, "item_7_full_name_3": {"attribute_name": "著者別名", "attribute_value_mlt": [{"nameIdentifiers": [{"nameIdentifier": "138325", "nameIdentifierScheme": "WEKO"}], "names": [{"name": "Koide, Takehiko"}]}]}, "item_7_publisher_7": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "新潟医学会"}]}, "item_7_select_19": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_select_item": "publisher"}]}, "item_7_source_id_11": {"attribute_name": "書誌レコードID", "attribute_value_mlt": [{"subitem_source_identifier": "AN00182415", "subitem_source_identifier_type": "NCID"}]}, "item_7_source_id_9": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "00290440", "subitem_source_identifier_type": "ISSN"}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "小出, 武比古"}], "nameIdentifiers": [{"nameIdentifier": "138324", "nameIdentifierScheme": "WEKO"}]}]}, "item_files": {"attribute_name": "ファイル情報", "attribute_type": "file", "attribute_value_mlt": [{"accessrole": "open_date", "date": [{"dateType": "Available", "dateValue": "2019-08-19"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "103(6)_457-461.pdf", "filesize": [{"value": "998.9 kB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 998900.0, "url": {"label": "103(6)_457-461.pdf", "url": "https://niigata-u.repo.nii.ac.jp/record/22874/files/103(6)_457-461.pdf"}, "version_id": "3d3e0bbd-cda8-4377-b513-007411f8102c"}]}, "item_keyword": {"attribute_name": "キーワード", "attribute_value_mlt": [{"subitem_subject": "RFLP", "subitem_subject_scheme": "Other"}, {"subitem_subject": "DNA diagnosis", "subitem_subject_scheme": "Other"}, {"subitem_subject": "prenatal diagnosis", "subitem_subject_scheme": "Other"}, {"subitem_subject": "carrier detection", "subitem_subject_scheme": "Other"}, {"subitem_subject": "hemophilias", "subitem_subject_scheme": "Other"}, {"subitem_subject": "多型性", "subitem_subject_scheme": "Other"}, {"subitem_subject": "DNA診断", "subitem_subject_scheme": "Other"}, {"subitem_subject": "胎児診断", "subitem_subject_scheme": "Other"}, {"subitem_subject": "保因者診断", "subitem_subject_scheme": "Other"}, {"subitem_subject": "血友病", "subitem_subject_scheme": "Other"}]}, "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": "departmental bulletin paper", "resourceuri": "http://purl.org/coar/resource_type/c_6501"}]}, "item_title": "5) 血友病のDNA診断(シンポジウム 遺伝子工学による病因解析とその診断, 第435回新潟医学会)", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "5) 血友病のDNA診断(シンポジウム 遺伝子工学による病因解析とその診断, 第435回新潟医学会)"}, {"subitem_title": "5) 血友病のDNA診断(シンポジウム 遺伝子工学による病因解析とその診断, 第435回新潟医学会)", "subitem_title_language": "en"}]}, "item_type_id": "7", "owner": "1", "path": ["456", "1209"], "permalink_uri": "http://hdl.handle.net/10191/41293", "pubdate": {"attribute_name": "公開日", "attribute_value": "2016-04-11"}, "publish_date": "2016-04-11", "publish_status": "0", "recid": "22874", "relation": {}, "relation_version_is_last": true, "title": ["5) 血友病のDNA診断(シンポジウム 遺伝子工学による病因解析とその診断, 第435回新潟医学会)"], "weko_shared_id": null}