The corresponding code for our paper: A sequence-to-sequence approach for document-level relation extraction. Check out our demo here!
The easiest way to get started is to follow along with one of our notebooks:
- Training your own model
- Reproducing results
Or to open the demo:
Note: Unfortunately, the demo is liable to crash as the free resources provided by Streamlit are insufficient to run the model. To run the demo locally, please follow the instructions below.
This repository requires Python 3.8 or later.
Before installing, you should create and activate a Python virtual environment. If you need pointers on setting up a virtual environment, please see the AllenNLP install instructions.
If you do not plan on modifying the source code, install from git using pip
pip install git+https://github.com/JohnGiorgi/seq2rel.gitOtherwise, clone the repository and install from source using Poetry:
# Install poetry for your system: https://python-poetry.org/docs/#installation
# E.g. for Linux, macOS, Windows (WSL)
curl -sSL https://install.python-poetry.org | python3 -
# Clone and move into the repo
git clone https://github.com/JohnGiorgi/seq2rel
cd seq2rel
# Install the package with poetry
poetry installDatasets are tab-separated files where each example is contained on its own line. The first column contains the text, and the second column contains the relations. Relations themselves must be serialized to strings.
Take the following example, which expresses a gene-disease association ("@GDA@") between ESR1 ("@GENE@") and schizophrenia ("@DISEASE@")
Variants in the estrogen receptor alpha (ESR1) gene and its mRNA contribute to risk for schizophrenia. estrogen receptor alpha ; ESR1 @GENE@ schizophrenia @DISEASE@ @GDA@
For convenience, we provide a second package, seq2rel-ds, which makes it easy to generate data in this format for various popular corpora. See our paper for more details on serializing relations.
To train the model, use the allennlp train command with one of our configs (or write your own!)
For example, to train a model on the BioCreative V CDR task corpus, first, preprocess this data with seq2rel-ds
seq2rel-ds cdr main "path/to/preprocessed/cdr"Then, call allennlp train with the CDR config we have provided
train_data_path="path/to/preprocessed/cdr/train.tsv" \
valid_data_path="path/to/preprocessed/cdr/valid.tsv" \
dataset_size=500 \
allennlp train "training_config/cdr.jsonnet" \
--serialization-dir "output" \
--include-package "seq2rel" The best model checkpoint (measured by micro-F1 score on the validation set), vocabulary, configuration, and log files will be saved to --serialization-dir. This can be changed to any directory you like. Please see the training notebook for more details.
To use the model to extract relations, import Seq2Rel and pass it some text
from seq2rel import Seq2Rel
from seq2rel.common import util
# Pretrained models are stored on GitHub and will be downloaded and cached automatically.
# See: https://github.com/JohnGiorgi/seq2rel/releases/tag/pretrained-models.
pretrained_model = "gda"
# Models are loaded via a simple interface
seq2rel = Seq2Rel(pretrained_model)
# Flexible inputs. You can provide...
# - a string
# - a list of strings
# - a text file (local path or URL)
input_text = "Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease (PD)."
# Pass any of these to the model to generate the raw output
output = seq2rel(input_text)
output == ["monoamine oxidase b ; maob @GENE@ parkinson's disease ; pd @DISEASE@ @GDA@"]
# To get a more structured (and useful!) output, use the `extract_relations` function
extract_relations = util.extract_relations(output)
extract_relations == [
{
"GDA": [
((("monoamine oxidase b", "maob"), "GENE"),
(("parkinson's disease", "pd"), "DISEASE"))
]
}
]See the list of available PRETRAINED_MODELS in seq2rel/seq2rel.py
python -c "from seq2rel import PRETRAINED_MODELS ; print(list(PRETRAINED_MODELS.keys()))"To run the demo locally, you will need to additionally install streamlit and pyvis (see here), then
streamlit run demo.pyTo reproduce the main results of the paper, use the allennlp evaluate command with one of our pretrained models
For example, to reproduce our results on the BioCreative V CDR task corpus, first, preprocess this data with seq2rel-ds
seq2rel-ds cdr main "path/to/preprocessed/cdr"Then, call allennlp evaluate with the pretrained CDR model
allennlp evaluate "https://github.com/JohnGiorgi/seq2rel/releases/download/pretrained-models/cdr.tar.gz" \
"path/to/preprocessed/cdr/test.tsv" \
--output-file "output/test_metrics.jsonl" \
--cuda-device 0 \
--predictions-output-file "output/test_predictions.jsonl" \
--include-package "seq2rel"The results and predictions will be saved to --output-file and --predictions-output-file. Please see the reproducing-results notebook for more details.
If you use seq2rel in your work, please consider citing our paper:
@inproceedings{giorgi-etal-2022-sequence,
title = {A sequence-to-sequence approach for document-level relation extraction},
author = {Giorgi, John and Bader, Gary and Wang, Bo},
year = 2022,
month = may,
booktitle = {Proceedings of the 21st Workshop on Biomedical Language Processing},
publisher = {Association for Computational Linguistics},
address = {Dublin, Ireland},
pages = {10--25},
doi = {10.18653/v1/2022.bionlp-1.2},
url = {https://aclanthology.org/2022.bionlp-1.2}
}
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