Traditional Chinese medicine, as an essential component of traditional medicine, contains active ingredients that serve as a crucial source for modern drug development, holding immense therapeutic potential and development value. A multi-layered and complex network is formed from Chinese medicine to diseases and used to predict the potential associations between Chinese medicine ingredients and diseases. This study proposes an ingredient-disease association prediction model (Node2Vec-DGI-EL) based on hierarchical graph representation learning. First, the model uses the Node2Vec algorithm to extract node embedding vectors from the network as the initial features of the nodes. Next, the network nodes are deeply represented and learned using the DGI algorithm to enhance the model's expressive power. To improve prediction accuracy and robustness, an ensemble learning method is incorporated to achieve more accurate ingredient-disease association predictions. The effectiveness of the model is then evaluated through a series of theoretical verifications. The results demonstrated that the proposed model significantly outperformed existing methods, achieving an AUC of 0.9987 and an AUPR of 0.9545, thereby indicating superior predictive capability. Ablation experiments further revealed the contribution and importance of each module. Additionally, case studies explored potential associations, such as triptonide with hypertensive retinopathy and methyl ursolate with colorectal cancer. Molecular docking experiments validated these findings, showing the triptonide-PGR interaction and the methyl ursolate-NFE2L2 interaction can bind stable. In conclusion, the Node2Vec-DGI-EL model focuses on TCM datasets and effectively predicts ingredient-disease associations, overcoming the reliance on node semantic information.

Comorbidity, the co-occurrence of multiple medical conditions in a single patient, profoundly impacts disease management and outcomes. Understanding these complex interconnections is crucial, especially in contexts where comorbidities exacerbate outcomes. Leveraging insights from the human interactome (HI) and advancements in graph-based methodologies, this study introduces Transformer with Subgraph Positional Encoding (TSPE) for disease comorbidity prediction. Inspired by Biologically Supervised Embedding (BSE), TSPE employs Transformer's attention mechanisms and Subgraph Positional Encoding (SPE) to capture interactions between nodes and disease associations. Our proposed SPE proves more effective than LPE, as used in Dwivedi et al.'s Graph Transformer, underscoring the importance of integrating clustering and disease-specific information for improved predictive accuracy. Evaluated on real clinical benchmark datasets (RR0 and RR1), TSPE demonstrates substantial performance enhancements over the state-of-the-art method, achieving up to 28.24% higher ROC AUC and 4.93% higher accuracy. This method shows promise for adaptation to other complex graph-based tasks and applications. The source code is available in the GitHub repository at: https://github.com/xihan-qin/TSPE-GraphTransformer.

Comorbidity carries significant implications for disease understanding and management. The genetic causes for comorbidity often trace back to mutations occurred either in the same gene associated with two diseases or in different genes associated with different diseases respectively but coming into connection via protein-protein interactions. Therefore, human interactome has been used in more sophisticated study of disease comorbidity. Human interactome, as a large incomplete graph, presents its own challenges to extracting useful features for comorbidity prediction. In this work, we introduce a novel approach named Biologically Supervised Graph Embedding (BSE) to allow for selecting most relevant features to enhance the prediction accuracy of comorbid disease pairs. Our investigation into BSE's impact on both centered and uncentered embedding methods showcases its consistent superiority over the state-of-the-art techniques and its adeptness in selecting dimensions enriched with vital biological insights, thereby improving prediction performance significantly, up to 50% when measured by ROC for some variations. Further analysis indicates that BSE consistently and substantially improves the ratio of disease associations to gene connectivity, affirming its potential in uncovering latent biological factors affecting comorbidity. The statistically significant enhancements across diverse metrics underscore BSE's potential to introduce novel avenues for precise disease comorbidity predictions and other potential applications. The GitHub repository containing the source code can be accessed at the following link: https://github.com/xihan-qin/Biologically-Supervised-Graph-Embedding.

Motivation: MiRNAs are a kind of small non - coding RNAs that are not translated into proteins, and aberrant expression of miRNAs is associated with human diseases. Since miRNAs have different roles in diseases, the miRNA - disease associations are categorized into multiple types according to their roles. Predicting miRNA - disease associations and types is critical to understand the underlying patho genesis of human diseases from the molecular level . Results: In this paper, we formulate the problem as a link prediction in knowledge graphs. We use biomedical knowledge bases to build a knowledge graph of entities representing miRNAs and disease and mult i - relations, and we propose a tensor decomposition - based model named TDRC to predict miRNA - disease associations and their types from the knowledge graph. We have experimentally evaluated our method and compared it to several baseline methods. The results d emonstrate that the proposed method h as high - accuracy and high - efficiency performances.

Knowledge-based biomedical data science (KBDS) involves the design and implementation of computer systems that act as if they knew about biomedicine. Such systems depend on formally represented knowledge in computer systems, often in the form of knowledge graphs. Here we survey the progress in the last year in systems that use formally represented knowledge to address data science problems in both clinical and biological domains, as well as on approaches for creating knowledge graphs. Major themes include the relationships between knowledge graphs and machine learning, the use of natural language processing, and the expansion of knowledge-based approaches to novel domains, such as Chinese Traditional Medicine and biodiversity.