Evidence map›Paper›PMID 30822516›Full record

ArticleMethods (San Diego, Calif.)2019

Exploring semi-supervised variational autoencoders for biomedical relation extraction.

Yijia Zhang, Zhiyong Lu

Abstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. COVID-19 Surveiller: toward a robust and effective pandemic surveillance system basedon social media mining.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2022
    Article
  8. Review
  9. Artificial intelligence-driven drug repurposing and structural biology for SARS-CoV-2.Current research in pharmacology and drug discovery · 2021
    Review
  10. Constructing knowledge graphs and their biomedical applications.Computational and structural biotechnology journal · 2020
    Review
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Yijia ZhangNational Center for Biotechnology Information (NCBI), National Library of Medicine (NLM), National Institutes of Health (NIH), Bethesda, MD 20894, USA; School of Computer Science and Technology, Dalian University of Technology, Dalian, Liaoning 116023, China.
Zhiyong LuNational Center for Biotechnology Information (NCBI), National Library of Medicine (NLM), National Institutes of Health (NIH), Bethesda, MD 20894, USA. Electronic address: zhiyong.lu@nih.gov.

Funding

Named Entity Recognition and Relationship Extraction in BiomedicineZIALM091813 · NLM · NATIONAL LIBRARY OF MEDICINE · PI LU, ZHIYONG · 2013 to 2022
$13.4M
Intramural NIH HHS Z99 LM999999
6 · The paper itself

Abstract

The biomedical literature provides a rich source of knowledge such as protein-protein interactions (PPIs), drug-drug interactions (DDIs) and chemical-protein interactions (CPIs). Biomedical relation extraction aims to automatically extract biomedical relations from biomedical text for various biomedical research. State-of-the-art methods for biomedical relation extraction are primarily based on supervised machine learning and therefore depend on (sufficient) labeled data. However, creating large sets of training data is prohibitively expensive and labor-intensive, especially so in biomedicine as domain knowledge is required. In contrast, there is a large amount of unlabeled biomedical text available in PubMed. Hence, computational methods capable of employing unlabeled data to reduce the burden of manual annotation are of particular interest in biomedical relation extraction. We present a novel semi-supervised approach based on variational autoencoder (VAE) for biomedical relation extraction. Our model consists of the following three parts, a classifier, an encoder and a decoder. The classifier is implemented using multi-layer convolutional neural networks (CNNs), and the encoder and decoder are implemented using both bidirectional long short-term memory networks (Bi-LSTMs) and CNNs, respectively. The semi-supervised mechanism allows our model to learn features from both the labeled and unlabeled data. We evaluate our method on multiple public PPI, DDI and CPI corpora. Experimental results show that our method effectively exploits the unlabeled data to improve the performance and reduce the dependence on labeled data. To our best knowledge, this is the first semi-supervised VAE-based method for (biomedical) relation extraction. Our results suggest that exploiting such unlabeled data can be greatly beneficial to improved performance in various biomedical relation extraction, especially when only limited labeled data (e.g. 2000 samples or less) is available in such tasks.

Indexed as

Neural Networks, ComputerAlgorithmsBiomedical ResearchData MiningDrug InteractionsProtein Interaction MapsSupervised Machine LearningBiomedical literatureRelation extractionSemi-supervised learningVariational autoencoder

Identifiers

PMID30822516
PMCPMC6708455

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.