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Know2BIO: A Comprehensive Dual-View Benchmark for Evolving Biomedical Knowledge Graphs

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arxiv 2310.03221 v1 pith:Z4QFTQ7W submitted 2023-10-05 cs.LG cs.AIq-bio.QM

classification cs.LGcs.AIq-bio.QM
keywords know2biobiomedicaldatabenchmarkknowledgemulti-modaldiversegraphs
verification ladder T0 review T1 audit T2 compute T3 formal
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Knowledge graphs (KGs) have emerged as a powerful framework for representing and integrating complex biomedical information. However, assembling KGs from diverse sources remains a significant challenge in several aspects, including entity alignment, scalability, and the need for continuous updates to keep pace with scientific advancements. Moreover, the representative power of KGs is often limited by the scarcity of multi-modal data integration. To overcome these challenges, we propose Know2BIO, a general-purpose heterogeneous KG benchmark for the biomedical domain. Know2BIO integrates data from 30 diverse sources, capturing intricate relationships across 11 biomedical categories. It currently consists of ~219,000 nodes and ~6,200,000 edges. Know2BIO is capable of user-directed automated updating to reflect the latest knowledge in biomedical science. Furthermore, Know2BIO is accompanied by multi-modal data: node features including text descriptions, protein and compound sequences and structures, enabling the utilization of emerging natural language processing methods and multi-modal data integration strategies. We evaluate KG representation models on Know2BIO, demonstrating its effectiveness as a benchmark for KG representation learning in the biomedical field. Data and source code of Know2BIO are available at https://github.com/Yijia-Xiao/Know2BIO/.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. Drift-Aware Temporal Graph Rewiring (DATGR) for Adaptive Semantic Modeling in Biomedical Text

    cs.AI 2026-07 conditional novelty 5.0 of 10

    DATGR updates co-occurrence edge weights via a logistic rule that mixes prior weight, current strength, change, and embedding drift, raising AUROC ~0.066 over a static baseline while holding AUPRC steady.

  2. Platform for Representation and Integration of multimodal Molecular Embeddings

    q-bio.BM 2025-07 conditional novelty 5.0 of 10

    An autoencoder-based platform merges nine gene embedding types into one 512-dimensional representation, with a permutation-adjusted SVCCA analysis showing the sources are largely complementary.

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