Evidence map›Paper›PMID 36767649›Full record

ArticleInternational journal of environmental research and public health2023

Automatic Text-Mining Approach to Identify Molecular Target Candidates Associated with Metabolic Processes for Myotonic Dystrophy Type 1.

Dhvani H Kuntawala, Filipa Martins, Rui Vitorino, Sandra Rebelo

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of environmental research and public health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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

4 authors at 1 institution in 1 country.

Dhvani H KuntawalaMedical Sciences Department, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-183 Aveiro, Portugal.ORCID 0000-0002-7813-8881
Filipa MartinsMedical Sciences Department, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-183 Aveiro, Portugal.ORCID 0000-0002-3277-1809
Rui VitorinoMedical Sciences Department, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-183 Aveiro, Portugal.ORCID 0000-0003-3636-5805
Sandra RebeloMedical Sciences Department, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-183 Aveiro, Portugal.ORCID 0000-0002-5862-5797
University of Aveiro · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myotonic dystrophy type 1 (DM1) is an autosomal dominant hereditary disease caused by abnormal expansion of unstable CTG repeats in the 3' untranslated region of the myotonic dystrophy protein kinase (

Indexed as

Myotonic DystrophyHumansMuscle, SkeletalMyotonin-Protein KinasePhosphatidylinositol 3-Kinasesrho-Associated KinasesSignal TransductionMyotonin-Protein KinasePhosphatidylinositol 3-Kinasesrho-Associated KinasesROCK1 protein, humanbibliometric analysisbioinformaticsfunctional enrichment analysismetabolismmyotonic dystrophy type 1VOSviewer

Identifiers

PMID36767649
PMCPMC9915907
OpenAlexW4318475368

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.