The Human Disease Ontology (DO) (www.disease-ontology.org) database, has significantly expanded the disease content and enhanced our userbase and website since the DO\u27s 2018 Nucleic Acids Research DATABASE issue paper. Conservatively, based on available resource statistics, terms from the DO have been annotated to over 1.5 million biomedical data elements and citations, a 10× increase in the past 5 years. The DO, funded as a NHGRI Genomic Resource, plays a key role in disease knowledge organization, representation, and standardization, serving as a reference framework for multiscale biomedical data integration and analysis across thousands of clinical, biomedical and computational research projects and genomic resources around the world....
Technological developments have resulted in tremendous increases in the volume and diversity of the ...
The Human Phenotype Ontology (HPO) is widely used in the rare disease community for differential dia...
Deep phenotyping has been defined as the precise and comprehensive analysis of phenotypic abnormalit...
peer reviewedThe current version of the Human Disease Ontology (DO) (http://www.disease-ontology.org...
The Disease Ontology (DO) is a community-driven, open source ontology designed for the semantic inte...
Model organisms are vital to uncovering the mechanisms of human disease and developing new therapeut...
The Human Phenotype Ontology (HPO)—a standardized vocabulary of phenotypic abnormalities associated ...
Presentation at the Biocuration 2018 conference: http://biocuration2018.cn/biocuration2018/<div><br>...
Bio-ontologies provide terminologies for the scientific community to describe biomedical entities in...
In this paper, we discuss an ontology-based system and approach that provides interoperability suppo...
Deep phenotyping has been defined as the precise and comprehensive analysis of phenotypic abnormalit...
BACKGROUND: The human genome has been extensively annotated with Gene Ontology for biological functi...
Summary: Disease Ontology (DO) annotates human genes in the context of disease. DO is important anno...
This is the final version of the article. Available from Oxford University Press via the DOI in this...
Technological developments have resulted in tremendous increases in the volume and diversity of the ...
The Human Phenotype Ontology (HPO) is widely used in the rare disease community for differential dia...
Deep phenotyping has been defined as the precise and comprehensive analysis of phenotypic abnormalit...
peer reviewedThe current version of the Human Disease Ontology (DO) (http://www.disease-ontology.org...
The Disease Ontology (DO) is a community-driven, open source ontology designed for the semantic inte...
Model organisms are vital to uncovering the mechanisms of human disease and developing new therapeut...
The Human Phenotype Ontology (HPO)—a standardized vocabulary of phenotypic abnormalities associated ...
Presentation at the Biocuration 2018 conference: http://biocuration2018.cn/biocuration2018/<div><br>...
Bio-ontologies provide terminologies for the scientific community to describe biomedical entities in...
In this paper, we discuss an ontology-based system and approach that provides interoperability suppo...
Deep phenotyping has been defined as the precise and comprehensive analysis of phenotypic abnormalit...
BACKGROUND: The human genome has been extensively annotated with Gene Ontology for biological functi...
Summary: Disease Ontology (DO) annotates human genes in the context of disease. DO is important anno...
This is the final version of the article. Available from Oxford University Press via the DOI in this...
Technological developments have resulted in tremendous increases in the volume and diversity of the ...
The Human Phenotype Ontology (HPO) is widely used in the rare disease community for differential dia...
Deep phenotyping has been defined as the precise and comprehensive analysis of phenotypic abnormalit...