Evidence map›Paper›PMID 35713857›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

Text Mining Protocol to Retrieve Significant Drug-Gene Interactions from PubMed Abstracts.

Sadhanha Anand, Oviya Ramalakshmi Iyyappan, Sharanya Manoharan, Dheepa Anand, Manonmani Alvin Jose, Raja Ravi Shanker

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
4.0field-weighted citation impact, top 6% of its field
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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 4 institutions in 1 country.

Sadhanha AnandDepartment of Biomedical Engineering, PSG College of Technology, Coimbatore, Tamilnadu, India.
Oviya Ramalakshmi Iyyappan *Department of Sciences, Amrita School of Engineering, Amrita Vishwa Vidyapeetham, Chennai, Tamilnadu, India.
Sharanya Manoharan *Department of Bioinformatics, Stella Maris College (Autonomous), Chennai, Tamilnadu, India.
Dheepa AnandDepartment of Pharmacology, Cheran College of Pharmacy, Coimbatore, Tamilnadu, India.
Manonmani Alvin JoseDepartment of Drugs Control, Govt. of Tamil Nadu, Tirunelveli, Tamilnadu, India.
Raja Ravi ShankerInternational Business Unit, Alembic Pharmaceuticals Limited, Vadodara, Gujarat, India. rajaravishanker@gmail.com.
Alembic Pharmaceuticals (India) · INAmrita Vishwa Vidyapeetham · INGovernment of Tamil Nadu · INPSG INSTITUTE OF TECHNOLOGY AND APPLIED RESEARCH · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genes and proteins form the basis of all cellular processes and ensure a smooth functioning of the human system. The diseases caused in humans can be either genetic in nature or may be caused due to external factors. Genetic diseases are mainly the result of any anomaly in gene/protein structure or function. This disruption interferes with the normal expression of cellular components. Against external factors, even though the immunogenicity of every individual protects them to a certain extent from infections, they are still susceptible to other disease-causing agents. Understanding the biological pathway/entities that could be targeted by specific drugs is an essential component of drug discovery. The traditional drug target discovery process is time-consuming and practically not feasible. A computational approach could provide speed and efficiency to the method. With the presence of vast biomedical literature, text mining also seems to be an obvious choice which could efficiently aid with other computational methods in identifying drug-gene targets. These could aid in initial stages of reviewing the disease components or can even aid parallel in extracting drug-disease-gene/protein relationships from literature. The present chapter aims at finding drug-gene interactions and how the information could be explored for drug interaction.

Indexed as

Data MiningDrug DiscoveryDrug InteractionsHumansPubMedADRDrug–disease–targetDrug–gene interactionFunctional annotationPolymorphismText mining

Identifiers

PMID35713857
OpenAlexW4285270693

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.