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Wytze J Vlietstra1, Rein Vos2,3, Marjan van den Akker4,5

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Identifying disease trajectories using knowledge graphs is enhanced by directional predicate information. This approach improves the accuracy of predicting sequential disease diagnoses, offering valuable insights into biomedical literature analysis.

Keywords:
Directionality of predicatesDisease trajectoriesKnowledge graphPredicatesProtein-protein interactionsTemporal relationships

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Area of Science:

  • Biomedical Informatics
  • Computational Biology
  • Data Science

Background:

  • Biomedical literature and databases can be represented using knowledge graphs with subject-predicate-object triples.
  • Disease trajectories, specific temporal sequences of disease diagnoses, are important for patient care.
  • Identifying these trajectories aids in understanding disease relationships.

Purpose of the Study:

  • To determine if disease sequences form trajectories using knowledge graph predicate information.
  • To evaluate the added value of directional information within predicates for trajectory identification.
  • To quantify performance improvements with and without directional predicate data.

Main Methods:

  • Constructed knowledge graphs from biomedical literature and databases.
  • Developed methods to represent indirect paths between disease-associated proteins.
  • Created feature sets with and without directional predicate information.
  • Compared classification performance using these feature sets.

Main Results:

  • Achieved a maximum area under the ROC curve of 89.8% and 74.5% with different reference sets.
  • Directional predicate information significantly improved performance by 6.5 and 2.0 percentage points, respectively.
  • Demonstrated the utility of predicate information for identifying disease trajectories.

Conclusions:

  • Predicates between proteins in knowledge graphs are effective for identifying disease trajectories.
  • Incorporating directional information of predicates substantially enhances prediction performance.
  • This method offers a novel approach to analyzing complex disease relationships in biomedical data.