Revision history of "GARD rare disease ID" (P4317)

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curprev 09:1909:19, 22 May 2024‎ Lombroso talk contribs‎ 20,771 bytes +89‎ ‎Added Japanese alias: GARD 希少疾患ID Tag: Wikidata user interface
curprev 09:1909:19, 22 May 2024‎ Lombroso talk contribs‎ 20,682 bytes +78‎ ‎Added [ja] label: GARD 稀少疾患ID Tag: Wikidata user interface

curprev 15:2315:23, 12 January 2024‎ Swpb talk contribs‎ 17,735 bytes −432‎ ‎Removed claim: Wikidata item of this property (P1629): Genetic and Rare Diseases Information Center (Q47517289), #quickstatements; #temporary_batch_1705072882496 Tag: quickstatements [2.0]

curprev 16:2616:26, 12 July 2023‎ TadejM talk contribs‎ 18,167 bytes +84‎ ‎Added [sl] label: oznaka redke bolezni GARD Tag: Wikidata user interface

curprev 02:3802:38, 13 April 2023‎ MidleadingBot talk contribs‎ 18,083 bytes +412‎ ‎Created claim: instance of (P31): numeric identifier (Q93868746), bot (details)

curprev 03:1803:18, 30 January 2023‎ RPI2026F1Bot talk contribs‎ 17,671 bytes +1,014‎ ‎Updated property: Updating information from Mix'n'Match (info) (details)

curprev 12:5612:56, 20 April 2022‎ Infrastruktur talk contribs‎ 16,657 bytes +120‎ ‎Added [nb] description: identifikator for sykdom i den amerikanske NIH GARD databasen Tag: Wikidata user interface
curprev 12:5612:56, 20 April 2022‎ Infrastruktur talk contribs‎ 16,537 bytes +65‎ ‎Added [nb] label: GARD ID Tag: Wikidata user interface

curprev 22:5122:51, 23 December 2021‎ Fierodelveneto talk contribs‎ 16,472 bytes +85‎ ‎Added [vec] label: ID GARD de małatia rara, #quickstatements; #temporary_batch_1640299837545 Tag: quickstatements [2.0]

curprev 01:4501:45, 14 September 2021‎ BrokenSegue talk contribs‎ 16,387 bytes +453‎ ‎Added reference to claim: URL match pattern (P8966): ^https?:\/\/rarediseases\.info\.nih\.gov\/diseases\/([1-9]\d*)\/index, batch #64559 Tag: quickstatements [2.0]

curprev 20:1620:16, 13 September 2021‎ BrokenSegue talk contribs‎ 15,934 bytes +407‎ ‎Created claim: URL match pattern (P8966): ^https?:\/\/rarediseases\.info\.nih\.gov\/diseases\/([1-9]\d*)\/index, batch #64559 Tag: quickstatements [2.0]

curprev 19:1819:18, 26 February 2021‎ Lockal talk contribs‎ 15,527 bytes +283‎ ‎Added qualifier: property scope (P5314): as reference (Q54828450), #quickstatements; #temporary_batch_1614352606418 Tag: quickstatements [2.0]
curprev 19:1819:18, 26 February 2021‎ Lockal talk contribs‎ 15,244 bytes +371‎ ‎Added qualifier: property scope (P5314): as main value (Q54828448), #quickstatements; #temporary_batch_1614352606418 Tag: quickstatements [2.0]
curprev 19:1819:18, 26 February 2021‎ Lockal talk contribs‎ 14,873 bytes +414‎ ‎Created claim: property constraint (P2302): property scope constraint (Q53869507), #quickstatements; #temporary_batch_1614352606418 Tags: Property constraint changed quickstatements [2.0]

curprev 17:5817:58, 27 January 2021‎ Epìdosis talk contribs‎ 14,459 bytes +432‎ ‎Created claim: applicable 'stated in' value (P9073): Genetic and Rare Diseases Information Center (Q47517289), batch #48493 Tag: quickstatements [2.0]

curprev 18:3918:39, 30 September 2020‎ Lockal talk contribs‎ 14,027 bytes +371‎ ‎Added qualifier: item of property constraint (P2305): Wikibase item (Q29934200), #quickstatements; #temporary_batch_1601482907053 Tag: quickstatements [2.0]
curprev 18:3918:39, 30 September 2020‎ Lockal talk contribs‎ 13,656 bytes +414‎ ‎Created claim: property constraint (P2302): allowed-entity-types constraint (Q52004125), #quickstatements; #temporary_batch_1601482907053 Tags: Property constraint changed quickstatements [2.0]

curprev 08:0208:02, 15 September 2020‎ Sezgin İbiş talk contribs‎ 13,242 bytes +272‎ ‎Added Turkish aliases: Genetik ve Nadir Hastalıklar Bilgi Merkezi Kimliği, GARD kimliği, GARD nadir hastalık kimliği
curprev 08:0208:02, 15 September 2020‎ Sezgin İbiş talk contribs‎ 12,970 bytes +218‎ ‎Added [tr] description: Birleşik Devletler Ulusal Genetik ve Nadir Hastalıklar Enstitüleri (GARD) Bilgi Merkezi veri tabanında nadir görülen bir hastalığın tanımlayıcısı
curprev 08:0208:02, 15 September 2020‎ Sezgin İbiş talk contribs‎ 12,752 bytes +131‎ ‎Added [tr] label: ABD Genetik ve Nadir Hastalıklar Bilgi Merkezi nadir hastalık kimliği

curprev 12:4912:49, 12 June 2020‎ Epìdosis talk contribs‎ 12,621 bytes +193‎ ‎Added [it] description: identificativo di una malattia rara nel database dello United States National Institutes of Health's Genetic and Rare Diseases (GARD)
curprev 12:4912:49, 12 June 2020‎ Epìdosis talk contribs‎ 12,428 bytes +1‎ ‎Changed Italian label: identificativo GARD di una malattia rara

curprev 13:0613:06, 13 February 2020‎ Osteologia talk contribs‎ 12,427 bytes +94‎ ‎Added [eo] label: numero de malofta malsano laŭ GARD

curprev 21:1921:19, 28 January 2020‎ Andrawaag talk contribs‎ 12,333 bytes +279‎ ‎Changed claim: property constraint (P2302): subject type constraint (Q21503250) Tag: Property constraint changed

curprev 21:1821:18, 17 December 2019‎ Adam Harangozó talk contribs‎ 12,054 bytes +318‎ ‎Changed claim: formatter URL (P1630): https://rarediseases.info.nih.gov/diseases/$1/index

curprev 23:3123:31, 19 November 2019‎ Adam Harangozó talk contribs‎ 11,736 bytes +360‎ ‎Changed claim: formatter URL (P1630): https://rarediseases.info.nih.gov/diseases/$1/index

curprev 20:2420:24, 5 September 2019‎ Peter James talk contribs‎ 11,376 bytes +209‎ ‎Added [en-gb] description: identifier for a rare disease in the United States National Institutes of Health's Genetic and Rare Diseases (GARD) Information Center database
curprev 20:2420:24, 5 September 2019‎ Peter James talk contribs‎ 11,167 bytes +85‎ ‎Added [en-gb] label: GARD rare disease ID

curprev 01:1801:18, 7 April 2019‎ Obsuser talk contribs‎ 11,082 bytes +75‎ ‎Added Serbian alias: GARD ID
curprev 01:1801:18, 7 April 2019‎ Obsuser talk contribs‎ 11,007 bytes +92‎ ‎Added [sr] label: GARD ID ретке болести

curprev 13:2713:27, 16 February 2019‎ Davidpar talk contribs‎ 10,915 bytes +94‎ ‎Added [ca] label: identificador GARD de malaltia rara

curprev 09:4809:48, 6 February 2019‎ Taravyvan Adijene talk contribs‎ 10,821 bytes +114‎ ‎Added Belarusian (Taraškievica orthography) alias: ідэнтыфікатар GARD
curprev 09:4809:48, 6 February 2019‎ Taravyvan Adijene talk contribs‎ 10,707 bytes +333‎ ‎Added [be-tarask] description: ідэнтыфікатар рэдкай хваробы у базе зьвестак Інфармацыйнага цэнтру Нацыянальнага інстытуту генэтычнага здароўя і рэдкіх захворваньняў ЗША
curprev 09:4809:48, 6 February 2019‎ Taravyvan Adijene talk contribs‎ 10,374 bytes +133‎ ‎Added [be-tarask] label: ідэнтыфікатар рэдкай хваробы GARD

curprev 11:4711:47, 31 January 2019‎ Thierry Caro talk contribs‎ 10,241 bytes +70‎ ‎Added French alias: identifiant GARD
curprev 11:4711:47, 31 January 2019‎ Thierry Caro talk contribs‎ 10,171 bytes +24‎ ‎Changed French label: identifiant Genetic and Rare Diseases Information Center

curprev 11:2711:27, 8 August 2018‎ Modeum talk contribs‎ 10,147 bytes +65‎ ‎Added [nn] label: GARD-id

curprev 17:2317:23, 25 May 2018‎ QuickStatementsBot talk contribs‎ 10,082 bytes −1,385‎ ‎Removed claim: property constraint (P2302): property scope constraint (Q53869507), #quickstatements; batch #2640 by User:Pintoch

curprev 21:3121:31, 22 May 2018‎ KrBot talk contribs‎ 11,467 bytes +283‎ ‎Added qualifier: constraint scope (P4680): constraint checked on references (Q46466805)

curprev 20:0820:08, 21 May 2018‎ KrBot talk contribs‎ 11,184 bytes 0‎ ‎Set a claim value: property constraint (P2302): property scope constraint (Q53869507)
curprev 20:0820:08, 21 May 2018‎ KrBot talk contribs‎ 11,184 bytes +317‎ ‎Added qualifier: constraint scope (P4680): constraint checked on main value (Q46466787)
curprev 06:3006:30, 21 May 2018‎ KrBot talk contribs‎ 10,867 bytes +371‎ ‎Added qualifier: constraint status (P2316): mandatory constraint (Q21502408)
curprev 06:3006:30, 21 May 2018‎ KrBot talk contribs‎ 10,496 bytes +414‎ ‎Created claim: property constraint (P2302): used for values only constraint (Q21528958)

curprev 18:3218:32, 15 May 2018‎ Manu1400 talk contribs‎ 10,082 bytes −371‎ ‎Undo revision 680066227 by Manu1400 (talk) Tag: Undo

Retrieved from "https://www.wikidata.org/wiki/Property:P4317"

Revision history of "GARD rare disease ID" (P4317)

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