Evidence map›Paper›PMID 28750648›Full record

ArticleJournal of biomedical semantics2017

Towards a more molecular taxonomy of disease.

Jisoo Park, Benjamin J Hescott, Donna K Slonim

Abstract read
In one paragraph

Article in Journal of biomedical semantics, 2017. 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. Article
  4. 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

3 authors.

Jisoo ParkDepartment of Computer Science, Tufts University, 161 College Avenue, Medford, 02155, MA, USA. jisoo.park@tufts.edu.ORCID http://orcid.org/0000-0002-3077-1979
Benjamin J HescottDepartment of Computer Science, Tufts University, 161 College Avenue, Medford, 02155, MA, USA.
Donna K SlonimDepartment of Computer Science, Tufts University, 161 College Avenue, Medford, 02155, MA, USA.

Funding

A Molecular Assessment of the Consequences of Preterm BirthR01HD076140 · NICHD · TUFTS UNIVERSITY MEDFORD · PI SLONIM, DONNA K. · 2013 to 2017
$1.6M
NICHD NIH HHS R01 HD076140
6 · The paper itself

Abstract

backgroundDisease taxonomies have been designed for many applications, but they tend not to fully incorporate the growing amount of molecular-level knowledge of disease processes, inhibiting research efforts. Understanding the degree to which we can infer disease relationships from molecular data alone may yield insights into how to ultimately construct more modern taxonomies that integrate both physiological and molecular information.

resultsWe introduce a new technique we call Parent Promotion to infer hierarchical relationships between disease terms using disease-gene data. We compare this technique with both an established ontology inference method (CliXO) and a minimum weight spanning tree approach. Because there is no gold standard molecular disease taxonomy available, we compare our inferred hierarchies to both the Medical Subject Headings (MeSH) category C forest of diseases and to subnetworks of the Disease Ontology (DO). This comparison provides insights about the inference algorithms, choices of evaluation metrics, and the existing molecular content of various subnetworks of MeSH and the DO. Our results suggest that the Parent Promotion method performs well in most cases. Performance across MeSH trees is also correlated between inference methods. Specifically, inferred relationships are more consistent with those in smaller MeSH disease trees than larger ones, but there are some notable exceptions that may correlate with higher molecular content in MeSH.

conclusionsOur experiments provide insights about learning relationships between diseases from disease genes alone. Future work should explore the prospect of disease term discovery from molecular data and how best to integrate molecular data with anatomical and clinical knowledge. This study nonetheless suggests that disease gene information has the potential to form an important part of the foundation for future representations of the disease landscape.

Indexed as

Biological OntologiesDiseaseHumansMedical Subject HeadingsReproducibility of ResultsDisease gene associationDisease OntologyDisease Ontology inferenceDisease tree inferenceHierarchical clusteringMedical Subject Headings treePairwise disease similarityParent Promotion

Identifiers

PMID28750648
PMCPMC5530939

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.