Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Entity/quality-based logical definitions for the human skeletal phenome using PATO.

Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference - 1 Jan 2009

Gkoutos Georgios V, Mungall Chris, Dolken Sandra, Ashburner Michael, Lewis Suzanna, Hancock John, Schofield Paul, Kohler Sebastian, Robinson Peter N

Abstract excerpt

This paper describes an approach to providing computer-interpretable logical definitions for the terms of the Human Phenotype Ontology (HPO) using PATO, the ontology of phenotypic qualities, to link terms of the HPO to the anatomic and other entities that are affected by abnormal phenotypic quali...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Computational Biology
Share to Marfan Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Models, Anatomic

Share to Phenotype

Share to Species Specificity

Share to Vocabulary, Controlled

Source

Open in PubMed Open full text

Identifiers

PMID: 19964203
DOI: 10.1109/IEMBS.2009.5333362
PMCID: PMC3398700

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19964203-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Entity/quality-based logical definitions for the human skeletal phenome using PATO.PMID 19964203Read ↗

The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease.Semantic proximity Read ↗

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.Semantic proximity Read ↗

Supervised segmentation of phenotype descriptions for the human skeletal phenome using hybrid methods.Semantic proximity Read ↗

Interoperability between phenotype and anatomy ontologies.Semantic proximity Read ↗

The human phenotype ontology.Semantic proximity Read ↗

The Xenopus Phenotype Ontology: bridging model organism phenotype data to human health and developmentSemantic proximity Read ↗

Identification of Associated Genes and Diseases in Patients With Congenital Upper-Limb Anomalies: A Novel Application of the OMT Classification.Semantic proximity Read ↗

Human Phenotype Ontology Annotations for Rare Congenital Conditions: Application to Arthrogryposis Multiplex Congenita.Semantic proximity Read ↗

The Xenopus phenotype ontology: bridging model organism phenotype data to human health and development.Semantic proximity Read ↗

PhenomeNET: a whole-phenome approach to disease gene discovery.Semantic proximity Read ↗

The Bone Dysplasia Ontology: integrating genotype and phenotype information in the skeletal dysplasia domain.Semantic proximity Read ↗

Linking human diseases to animal models using ontology-based phenotype annotation.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.