Text embedding models are essential for various natural language processing tasks, enabling the effective encoding of semantic information into dense vector representations. These models are typically optimized using triplets of (query, positive, negative) data pairs for contrastive learning, where the negative samples play a critical role in enhancing the model’s ability to discern subtle semantic distinctions. In this work, we introduce a **M**ulti-**G**ranularity **H**ard-negative (MGH) synthesis framework that leverages large language models (LLMs) to generate diverse negative samples with varying levels of similarity with the query. This approach facilitates a coarse-to-fine curriculum learning strategy during supervised training, allowing the embedding model to progressively learn more nuanced semantic representations. Meanwhile, we propose an **A**nchor **T**oken **A**ware (ATA) pooling method that assigns higher weights to anchor tokens based on aggregation patterns observed in LLMs, improving text embedding accuracy without increasing model complexity. Comprehensive experiments on the MTEB benchmark demonstrate that our methods achieve state-of-the-art performance, surpassing existing synthesis strategies both with synthetic data and when combined with public retrieval datasets.

The ever-growing biomedical publications magnify the challenge of extracting structured data from unstructured texts. This task involves two components: biomedical entity identification (Named Entity Recognition, NER) and their interrelation determination (Relation Extraction, RE). However, existing methods often neglect unique features of the biomedical literature, such as ambiguous entities, nested proper nouns, and overlapping relation triplets, and underutilize prior knowledge, leading to an intolerable performance decline in the biomedical domain, especially with limited annotated training data. In this paper, we propose the Biomedical Relation-First eXtraction (Bio-RFX) model by leveraging sentence-level relation classification before entity extraction to tackle entity ambiguity. Moreover, we exploit structural constraints between entities and relations to guide the model’s hypothesis space, enhancing extraction performance across different training scenarios. Comprehensive experimental results on biomedical datasets show that Bio-RFX achieves significant improvements on both NER and RE tasks. Even under the low-resource training scenarios, it outperforms all baselines in NER and has highly competitive performance compared to the state-of-the-art fine-tuned baselines in RE.

Document-level relation extraction (DocRE) aims to identify semantic labels among entities within a single document. One major challenge of DocRE is to dig decisive details regarding a specific entity pair from long text. However, in many cases, only a fraction of text carries required information, even in the manually labeled supporting evidence. To better capture and exploit instructive information, we propose a novel expLicit syntAx Refinement and Subsentence mOdeliNg based framework (LARSON). By introducing extra syntactic information, LARSON can model subsentences of arbitrary granularity and efficiently screen instructive ones. Moreover, we incorporate refined syntax into text representations which further improves the performance of LARSON. Experimental results on three benchmark datasets (DocRED, CDR, and GDA) demonstrate that LARSON significantly outperforms existing methods.