Evidence map›Paper›PMID 40996710›Full record

ArticleDatabase : the journal of biological databases and curation2025

Biomedical literature-based clinical phenotype definition discovery using large language models.

Samar Binkheder, Xiaofu Liu, Michael Wu, Lei Wang, Aditi Shendre, Sara K Quinney, Wei-Qi Wei, Lang Li

Abstract read
In one paragraph

Article in Database : the journal of biological databases and curation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Samar BinkhederMedical Informatics Unit, Department of Medical Education, College of Medicine, King Saud University, Riyadh 12372, Saudi Arabia.ORCID 0000-0003-0400-823X
Xiaofu LiuDepartment of Biomedical Informatics,, College of Medicine, Ohio State University, 1800 Cannon Drive, Columbus, OH 43210, United States.
Michael WugRED Computational Sciences, Computational Biology & Translation, Genentech, Inc, 1 DNA Way, South San Francisco, CA 94080, United States.
Lei WangDepartment of Biomedical Informatics,, College of Medicine, Ohio State University, 1800 Cannon Drive, Columbus, OH 43210, United States.ORCID 0000-0003-1904-1737
Aditi ShendreDepartment of Biomedical Informatics,, College of Medicine, Ohio State University, 1800 Cannon Drive, Columbus, OH 43210, United States.
Sara K QuinneyDepartment of Obstetrics and Gynecology, School of Medicine, Indiana University, 950 W Walnut Street, Indianapolis, IN 46202, United States.ORCID 0000-0002-6554-0695
Wei-Qi WeiDepartment of Biomedical Informatics, Vanderbilt University Medical Center, 2525 West End Ave, Nashville, TN 37203, United States.
Lang LiDepartment of Biomedical Informatics,, College of Medicine, Ohio State University, 1800 Cannon Drive, Columbus, OH 43210, United States.ORCID 0000-0002-0746-1809

Funding

The Indiana University-Ohio State University Maternal and Pediatric Precision in Therapeutics Data, Model, Knowledge, and Research Coordination Center (IU-OSU MPRINT DMKRCC)P30HD106451 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI Lang Li, Sara K Quinney · 2021 to 2026
$24.1M
Clinical Importance of Drug-Drug InteractionsR01AG025152 · NIA · UNIVERSITY OF PENNSYLVANIA · PI HENNESSY, SEAN, LI, LANG · 2006 to 2021
$8.1M
Statistical and Machine Learning Methods to Improve Dynamic Treatment Regimens Estimation Using Real World Data.R01GM124104 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Yuanjia Wang, Donglin Zeng · 2018 to 2026
$3.1M
Machine learning drives translational research from drug interactions to pharmacogeneticsR01LM014199 · NLM · OHIO STATE UNIVERSITY · PI You Chen, Lang Li · 2023 to 2026
$2.5M
Evidence-based Drug-Interaction Discovery: In-Vivo, In-Vitro and ClinicalR01LM011945 · NLM · INDIANA UNIVERSITY INDIANAPOLIS · PI LI, LANG, ROCHA, LUIS M · 2014 to 2017
$1.8M
A Translational Bioinformatics Approach in the Drug Interaction ResearchR01GM104483 · NIGMS · OHIO STATE UNIVERSITY · PI LI, LANG · 2014 to 2017
$1.5M
Integrated bioinformatic and pharmacokinetic models of high-dimensional drug interactionsR01GM117206 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI QUINNEY, SARA K · 2016 to 2018
$1.1M
An informatics bridge over the valley of death for cancer Phase I trials of drug-combination therapiesU01CA248240 · NCI · OHIO STATE UNIVERSITY · PI LI, LANG · 2021 to 2023
$1.1M
NCI NIH HHS U01 CA248240NIA NIH HHS R01 AG025152NICHD NIH HHS P30 HD106451NIGMS NIH HHS R01 GM104483NIGMS NIH HHS R01 GM117206NIGMS NIH HHS R01 GM124104NLM NIH HHS R01 LM011945NLM NIH HHS R01 LM014199
6 · The paper itself

Abstract

Electronic health record (EHR) phenotyping is a high-demand task because most phenotypes are not usually readily defined. The objective of this study is to develop an effective text-mining approach that automatically extracts clinical phenotype definitions-related sentences from biomedical literature. Abstract-level and full-text sentence-level classifiers were developed for clinical phenotype discovery from PubMed. We compared the performance of the abstract-level classifier on machine learning algorithms: support vector machine (SVM), logistic regression (LR), naïve Bayes, and decision tree. SVM classifier showed the best performance (F-measure = 98%) in identifying clinical phenotype-relevant abstracts. It predicted 459 406 clinical phenotype-related abstracts. For the full-text sentence-level classifier, we compared the performance of SVM, LR, naïve Bayes, decision trees, convolutional neural networks, Bidirectional Encoder Representations from Transformers (BERT), and Bidirectional Encoder Representations from Transformers for Biomedical Text Mining (BioBERT). BioBERT model was the best performer among the full-text sentence-level classifiers (F-measure = 91%). We used these two optimal classifiers for large-scale screening of the PubMed database, starting with abstract retrieval and followed by predicting clinical phenotype-related sentences from full texts. The large-scale screening predicted over two million clinical phenotype-related sentences. Lastly, we developed a knowledgebase using positively predicted sentences, allowing users to query clinical phenotype-related sentences with a phenotype term of interest. The Clinical Phenotype Knowledgebase (CliPheKB) enables users to search for clinical phenotype terms and retrieve sentences related to a specific clinical phenotype of interest (https://cliphekb.shinyapps.io/phenotype-main/). Building upon prior methods, we developed a text mining pipeline to automatically extract clinical phenotype definition-related sentences from the literature. This high-throughput phenotyping approach is generalizable and scalable, and it is complementary to existing EHR phenotyping methods.

Indexed as

Data MiningPhenotypeAlgorithmsBayes TheoremDecision TreesElectronic Health RecordsHumansLanguageLarge Language ModelsMachine LearningNatural Language ProcessingPubMedSupport Vector Machine

Identifiers

PMID40996710
PMCPMC12462612

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.