| test3 | | | 10.7 K | | ykyao | 2023-11-29 | | |
| BLAH2015_Annotations_test_5 | | | 1.34 K | nestoralvaro | nestoralvaro | 2023-11-30 | Testing | |
| GO-MF | | Annotation for molecular functions as defined in the "Molecular Function" subtree of Gene Ontology | 19.7 K | DBCLS | Jin-Dong Kim | 2023-12-04 | Testing | |
| DLUT931 | | DLUT NLP Lab.Test our event extration result for 16 GE task. | 4.57 K | | DLUT931 | 2023-11-30 | Testing | |
| bionlp-st-ge-2016-reference | | It is the benchmark reference data set of the BioNLP-ST 2016 GE task.
It includes Genia-style event annotations to 20 full paper articles which are about NFκB proteins.
The task is to develop an automatic annotation system which can produce annotation similar to the annotation in this data set as much as possible.
For evaluation of the performance of a participating system, the system needs to produce annotations to the documents in the benchmark test data set (bionlp-st-ge-2016-test).
GE 2016 benchmark data set is provided as multi-layer annotations which include:
bionlp-st-ge-2016-reference: benchmark reference data set (this project)
bionlp-st-ge-2016-test: benchmark test data set (annotations are blined)
bionlp-st-ge-2016-test-proteins: protein annotation to the benchmark test data set
Following is supporting resources:
bionlp-st-ge-2016-coref: coreference annotation
bionlp-st-ge-2016-uniprot: Protein annotation with UniProt IDs.
pmc-enju-pas: dependency parsing result produced by Enju
UBERON-AE: annotation for anatomical entities as defined in UBERON
ICD10: annotation for disease names as defined in ICD10
GO-BP: annotation for biological process names as defined in GO
GO-CC: annotation for cellular component names as defined in GO
A SPARQL-driven search interface is provided at http://bionlp.dbcls.jp/sparql. | 14.4 K | DBCLS | Jin-Dong Kim | 2023-11-29 | Released | |
| test2 | | | 12.3 K | | ykyao | 2023-11-29 | | |
| events-check-again | | | 14.4 K | | | 2023-11-30 | Testing | |
| bionlp-st-2016-SeeDev-test | | Entities annotations from the test set of the BioNLP-ST 2016 SeeDev task.
SeeDev task focuses on seed storage and reserve accumulation on the model organism, Arabidopsis thaliana. The SeeDev task is based on the knowledge model Gene Regulation Network for Arabidopsis (GRNA) that meets the needs of text-mining (i.e. manual annotation of texts and automatic information extraction), experimental data indexing and retrieval and reuse in other plant systems. It is also expected to meet the requirements of the integration of the text knowledge with knowledge derived from experimental data in view of modeling in systems biology.
GRNA model defines 16 different types of entities, and 22 types of event (in five sets of event types) that may be combined in complex events.
For more information, please refer to the task website
All annotations :
Train set
Development set
Test set (without events)
| 184 | | EstelleChaix | 2023-11-29 | Released | |
| AnEM_full-texts | | 250 documents selected randomly from full-text papers
Entity types: organism subdivision, anatomical system, organ, multi-tissue structure, tissue, cell, developing anatomical structure, cellular component, organism substance, immaterial anatomical entity and pathological formation
Together with AnEM_abstracts, it is probably the largest manually annotated corpus on anatomical entities. | 687 | NaCTeM | Yue Wang | 2023-11-29 | Uploading | |
| Staphylococcus | | | 7.46 K | haruo | haruo | 2023-11-29 | Testing | |
| vtt_friends_s01e07 | | | 0 | | donghwan kim | 2023-11-24 | | |
| test10 | | | 212 | | Jin-Dong Kim | 2023-11-24 | | |
| tmVarCorpus | | Wei C-H, Harris BR, Kao H-Y, Lu Z (2013) tmVar: A text mining approach for extracting sequence variants in biomedical literature, Bioinformatics, 29(11) 1433-1439, doi:10.1093/bioinformatics/btt156. | 1.43 K | Chih-Hsuan Wei , Bethany R. Harris , Hung-Yu Kao and Zhiyong Lu | Chih-Hsuan Wei | 2023-11-24 | Released | |
| CoMAGC | | In order to access the large amount of information in biomedical literature about genes implicated in various cancers both efficiently and accurately, the aid of text mining (TM) systems is invaluable. Current TM systems do target either gene-cancer relations or biological processes involving genes and cancers, but the former type produces information not comprehensive enough to explain how a gene affects a cancer, and the latter does not provide a concise summary of gene-cancer relations. In order to support the development of TM systems that are specifically targeting gene-cancer relations but are still able to capture complex information in biomedical sentences, we publish CoMAGC, a corpus with multi- faceted annotations of gene-cancer relations. In CoMAGC, a piece of annotation is composed of four semantically orthogonal concepts that together express 1) how a gene changes, 2) how a cancer changes and 3) the causality between the gene and the cancer. The multi-faceted annotations are shown to have high inter-annotator agreement. In addition, the annotations in CoMAGC allow us to infer the prospective roles of genes in cancers and to classify the genes into three classes according to the inferred roles. We encode the mapping between multi-faceted annotations and gene classes into 10 inference rules. The inference rules produce results with high accuracy as measured against human annotations. CoMAGC consists of 821 sentences on prostate, breast and ovarian cancers. Currently, the corpus deals with changes in gene expression levels among other types of gene changes. | 1.53 K | Lee et al | Hee-Jin Lee | 2023-11-24 | Released | |
| proj_h_1 | | | 6.7 K | | | 2023-11-24 | | |
| jnlpba-st-training | | The training data used in the task came from the GENIA version 3.02 corpus, This was formed from a controlled search on MEDLINE using the MeSH terms "human", "blood cells" and "transcription factors". From this search, 1,999 abstracts were selected and hand annotated according to a small taxonomy of 48 classes based on a chemical classification. Among the classes, 36 terminal classes were used to annotate the GENIA corpus. For the shared task only the classes protein, DNA, RNA, cell line and cell type were used. The first three incorporate several subclasses from the original taxonomy while the last two are interesting in order to make the task realistic for post-processing by a potential template filling application. The publication year of the training set ranges over 1990~1999. | 51.1 K | GENIA | Yue Wang | 2023-11-26 | Released | |
| CyanoBase | | Cyanobacteria are prokaryotic organisms that have served as important model organisms for studying oxygenic photosynthesis and have played a significant role in the Earthfs history as primary producers of atmospheric oxygen.
Publication: http://www.aclweb.org/anthology/W12-2430 | 1.1 K | Kazusa DNA Research Institute and Database Center for Life Science (DBCLS) | Yue Wang | 2023-11-26 | Released | |
| bionlp-st-ge-2016-test-proteins | | Protein annotations to the benchmark test data set of the BioNLP-ST 2016 GE task.
A participant of the GE task may import the documents and annotations of this project to his/her own project, to begin with producing event annotations.
For more details, please refer to the benchmark test data set (bionlp-st-ge-2016-test).
| 4.34 K | DBCLS | Jin-Dong Kim | 2023-11-27 | Released | |
| disease_gene_microbe_small | | Small version (48 abstract that mention both Crohns and S. aureus) for development purposes
Abbreviation: dgm Content: annotated abstracts on Crohn’s disease or on on Staphylococcus aureus (according to the jensenlab.org indexing resources) Entity types: (three for a start, organisms (NCBI Taxonomy taxa), disease (Disease Ontology terms), human genes (ENSEMBL proteins) Aim: Explore indirect associations of diseases to microbial species in this corpus via gene co-mentions | 536 | | evangelos | 2023-11-27 | Testing | |
| consensus_PMA_Age_Indications | | | 1.7 K | | laurenc | 2023-11-28 | Beta | |
