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| Label | Examples |
|---|---|
| Data | "an overall mitochondrial", "defect", "Depth time - series" |
| Material | "cross - shore measurement locations", "the subject 's fibroblasts", "COXI , COXII and COXIII subunits" |
| Method | "EFSA", "an approximation", "in vitro" |
| Process | "translation", "intake", "a significant reduction of synthesis" |
| Label | Precision | Recall | F1 |
|---|---|---|---|
| all | 0.7199 | 0.6894 | 0.7043 |
| Data | 0.6224 | 0.6455 | 0.6338 |
| Material | 0.8061 | 0.7861 | 0.7960 |
| Method | 0.5789 | 0.55 | 0.5641 |
| Process | 0.7472 | 0.6488 | 0.6945 |
1from span_marker import SpanMarkerModel
2
3# Download from the 🤗 Hub
4model = SpanMarkerModel.from_pretrained("span-marker-malteos/scincl-me")
5# Run inference
6entities = model.predict("We established a P fertilizer need map based on integrating results from the two systems .")1from span_marker import SpanMarkerModel, Trainer
2
3# Download from the 🤗 Hub
4model = SpanMarkerModel.from_pretrained("span-marker-malteos/scincl-me")
5
6# Specify a Dataset with "tokens" and "ner_tag" columns
7dataset = load_dataset("conll2003") # For example CoNLL2003
8
9# Initialize a Trainer using the pretrained model & dataset
10trainer = Trainer(
11 model=model,
12 train_dataset=dataset["train"],
13 eval_dataset=dataset["validation"],
14)
15trainer.train()
16trainer.save_model("span-marker-malteos/scincl-me-finetuned")| Training set | Min | Median | Max |
|---|---|---|---|
| Sentence length | 3 | 25.6049 | 106 |
| Entities per sentence | 0 | 5.2439 | 22 |
@software{Aarsen_SpanMarker,
author = {Aarsen, Tom},
license = {Apache-2.0},
title = {{SpanMarker for Named Entity Recognition}},
url = {https://github.com/tomaarsen/SpanMarkerNER}
}