Abstract
Discussions on the development of data and information concerning Indigenous peoples have been occurring since the 1950s. The initial issues related to Indigenous data were recognized and addressed internationally through the United Nations International Labour Organization Conventions No.107 (1957) and No.169 (1989) [1, 2]. The 2007 United Nations Declaration on the Rights of Indigenous Peoples (UNDRIP) underscores the rights of Indigenous peoples to live in dignity; maintain and strengthen their institutions, cultures, and traditions; and pursue self-determined development based on Indigenous needs and aspirations [3]. This includes ensuring the quality and usability of Indigenous data to best serve the needs and aspirations of Indigenous peoples.
| Original language | English |
|---|---|
| Title of host publication | Indigenous and Tribal Peoples and Cancer |
| Editors | Gail Garvey, Linda Burhansstipanov, Lea Bill, Nina Scott, Lisa Whop |
| Place of Publication | Switzerland |
| Publisher | Springer Science+Business Media |
| Chapter | 9 |
| Pages | 41-45 |
| Number of pages | 5 |
| ISBN (Electronic) | 9783031568060 |
| ISBN (Print) | 9783031568053 |
| DOIs | |
| Publication status | Published - 2024 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Indigenous Data Sovereignty
- cancer reporting
- data
- Indigenous peoples
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