Evidence map›Paper›PMID 27278817›Full record

ArticleDatabase : the journal of biological databases and curation2016

Mining clinical attributes of genomic variants through assisted literature curation in Egas.

Sérgio Matos, David Campos, Renato Pinho, Raquel M Silva, Matthew Mort, David N Cooper, José Luís Oliveira

Abstract read
In one paragraph

Article in Database : the journal of biological databases and curation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Overview of the interactive task in BioCreative V.Database : the journal of biological databases and curation · 2016
    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

7 authors.

Sérgio MatosIEETA/DETI, University of Aveiro, Aveiro, 3810-193, Portugal aleixomatos@ua.pt.
David CamposBMD Software, Aveiro, Portugal.
Renato PinhoIEETA/DETI, University of Aveiro, Aveiro, 3810-193, Portugal.
Raquel M SilvaIEETA/DETI, University of Aveiro, Aveiro, 3810-193, Portugal Department of Medical Sciences, iBiMED, University of Aveiro, Aveiro, 3810-193, Portugal.
Matthew Mort
David N CooperInstitute of Medical Genetics, Cardiff University, Heath Park, Cardiff, UK.
José Luís OliveiraIEETA/DETI, University of Aveiro, Aveiro, 3810-193, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The veritable deluge of biological data over recent years has led to the establishment of a considerable number of knowledge resources that compile curated information extracted from the literature and store it in structured form, facilitating its use and exploitation. In this article, we focus on the curation of inherited genetic variants and associated clinical attributes, such as zygosity, penetrance or inheritance mode, and describe the use of Egas for this task. Egas is a web-based platform for text-mining assisted literature curation that focuses on usability through modern design solutions and simple user interactions. Egas offers a flexible and customizable tool that allows defining the concept types and relations of interest for a given annotation task, as well as the ontologies used for normalizing each concept type. Further, annotations may be performed on raw documents or on the results of automated concept identification and relation extraction tools. Users can inspect, correct or remove automatic text-mining results, manually add new annotations, and export the results to standard formats. Egas is compatible with the most recent versions of Google Chrome, Mozilla Firefox, Internet Explorer and Safari and is available for use at https://demo.bmd-software.com/egas/Database URL: https://demo.bmd-software.com/egas/.

Indexed as

InternetUser-Computer InterfaceWeb BrowserAnimalsData CurationData MiningHumans

Identifiers

PMID27278817
PMCPMC4897594

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.