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The Medical Action Ontology: A tool for annotating and analyzing treatments and clinical management of human disease.
Med. 2023 Dec 8;4(12):913-927.e3. doi: 10.1016/j.medj.2023.10.003. Epub 2023 Nov 13.
3
Leveraging Generative AI to Accelerate Biocuration of Medical Actions for Rare Disease.
medRxiv. 2024 Aug 22:2024.08.22.24310814. doi: 10.1101/2024.08.22.24310814.
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The Human Phenotype Ontology in 2024: phenotypes around the world.
Nucleic Acids Res. 2024 Jan 5;52(D1):D1333-D1346. doi: 10.1093/nar/gkad1005.
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[Rare-disease data standards].
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2022 Nov;65(11):1126-1132. doi: 10.1007/s00103-022-03591-2. Epub 2022 Sep 23.
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HPO2Vec+: Leveraging heterogeneous knowledge resources to enrich node embeddings for the Human Phenotype Ontology.
J Biomed Inform. 2019 Aug;96:103246. doi: 10.1016/j.jbi.2019.103246. Epub 2019 Jun 27.
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The Human Phenotype Ontology in 2021.
Nucleic Acids Res. 2021 Jan 8;49(D1):D1207-D1217. doi: 10.1093/nar/gkaa1043.
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MicrO: an ontology of phenotypic and metabolic characters, assays, and culture media found in prokaryotic taxonomic descriptions.
J Biomed Semantics. 2016 Apr 12;7:18. doi: 10.1186/s13326-016-0060-6. eCollection 2016.
10
Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity.
J Allergy Clin Immunol. 2022 Jan;149(1):369-378. doi: 10.1016/j.jaci.2021.04.033. Epub 2021 May 12.

引用本文的文献

1
Leveraging generative AI to assist biocuration of medical actions for rare disease.
Bioinform Adv. 2025 Jun 12;5(1):vbaf141. doi: 10.1093/bioadv/vbaf141. eCollection 2025.
3
Leveraging Generative AI to Accelerate Biocuration of Medical Actions for Rare Disease.
medRxiv. 2024 Aug 22:2024.08.22.24310814. doi: 10.1101/2024.08.22.24310814.
4
Current best practices and future opportunities for reproducible findings using large-scale neuroimaging in psychiatry.
Neuropsychopharmacology. 2024 Nov;50(1):37-51. doi: 10.1038/s41386-024-01938-8. Epub 2024 Aug 8.
5
Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions.
NPJ Genom Med. 2024 Apr 6;9(1):27. doi: 10.1038/s41525-024-00408-w.

本文引用的文献

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GA4GH Phenopackets: A Practical Introduction.
Adv Genet (Hoboken). 2022 Aug 25;4(1):2200016. doi: 10.1002/ggn2.202200016. eCollection 2023 Mar.
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Phenotype-aware prioritisation of rare Mendelian disease variants.
Trends Genet. 2022 Dec;38(12):1271-1283. doi: 10.1016/j.tig.2022.07.002. Epub 2022 Aug 4.
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The GA4GH Phenopacket schema defines a computable representation of clinical data.
Nat Biotechnol. 2022 Jun;40(6):817-820. doi: 10.1038/s41587-022-01357-4.
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A Review of Targeted Therapies for Monogenic Epilepsy Syndromes.
Front Neurol. 2022 Feb 17;13:829116. doi: 10.3389/fneur.2022.829116. eCollection 2022.
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A guide for the diagnosis of rare and undiagnosed disease: beyond the exome.
Genome Med. 2022 Feb 28;14(1):23. doi: 10.1186/s13073-022-01026-w.
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OBO Foundry in 2021: operationalizing open data principles to evaluate ontologies.
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Marfan syndrome.
Nat Rev Dis Primers. 2021 Sep 2;7(1):64. doi: 10.1038/s41572-021-00298-7.
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An Evidence-Based Framework for Evaluating Pharmacogenomics Knowledge for Personalized Medicine.
Clin Pharmacol Ther. 2021 Sep;110(3):563-572. doi: 10.1002/cpt.2350. Epub 2021 Jul 22.
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The Treatabolome, an emerging concept.
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