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source_datasets: - PubMed Central
STXBP1 PubMed Central Full-Text Dataset
Dataset Description
A comprehensive collection of 31,598 scientific articles from PubMed Central (PMC) related to STXBP1 (Syntaxin Binding Protein 1), Munc18-1, and associated neurological conditions. This dataset contains full-text articles where available, making it one of the most complete publicly available resources for STXBP1 research.
About STXBP1
STXBP1 (also known as Munc18-1) is a gene that encodes a protein essential for neurotransmitter release at synapses. Mutations in STXBP1 cause STXBP1 Encephalopathy, a rare neurological disorder characterized by:
- Early-onset epilepsy (often within the first months of life)
- Developmental delays and intellectual disability
- Movement disorders
- Autism spectrum features
STXBP1-related disorders affect approximately 1 in 30,000 live births, making research aggregation critically important for advancing understanding and developing treatments.
Dataset Details
Source
- Origin: PubMed Central (PMC) Open Access Subset
- Collection Date: June 2025
- Search Strategy: Articles matching STXBP1, Munc18, and related neurological/epilepsy terms
Content
| Field | Type | Description |
|---|---|---|
title |
string | Article title |
abstract |
string | Article abstract |
main_text |
string | Full article text (where available) |
authors |
string | Comma-separated author names |
pmid |
string | PubMed ID |
doi |
string | Digital Object Identifier |
publication_date |
string | Publication date |
journal |
string | Journal name |
keywords |
string | Comma-separated keywords |
stxbp1_count |
int | Count of "STXBP1" mentions in text |
munc18_count |
int | Count of "Munc18" mentions in text |
pmc_id |
string | PubMed Central ID |
url |
string | URL to original article |
download_date |
string | ISO timestamp of download |
source_file |
string | Original source filename |
STXBP Family Terms:
STXBP1, STXBP2, STXBP3, STXBP4, STXBP5, STXBP6, STXBP11 Munc18, Munc18-1, Munc-18, Munc 18 Munc18 syntaxin, syntaxin binding protein
CRISPR/Gene Therapy Terms:
CRISPR Cas9, CRISPR-Cas9, CRISPR/Cas9 CRISPR Cas12, CRISPR-Cas12, CRISPR/Cas12 CRISPR Cas13, CRISPR-Cas13 base editing, prime editing
Combination Searches:
STXBP1/Munc18/syntaxin binding protein combined with: CRISPR, gene therapy, gene editing, AAV, antisense
Statistics
- Total Articles: ~31,000
- Articles with Full Text: Majority (exact count varies)
- Date Range: Historical to June 2025
- Primary Language: English
Usage
Loading the Dataset
from datasets import load_dataset
# Load the full dataset
dataset = load_dataset("SkyWhal3/stxbp1-pubmed-fulltext")
# Access the data
for article in dataset['train']:
print(article['title'])
print(article['abstract'][:500])
Filtering for High-Relevance Articles
# Filter for articles that directly mention STXBP1
stxbp1_direct = dataset.filter(lambda x: x['stxbp1_count'] > 0)
# Filter for articles mentioning Munc18
munc18_articles = dataset.filter(lambda x: x['munc18_count'] > 0)
# High-relevance articles (multiple mentions)
high_relevance = dataset.filter(lambda x: x['stxbp1_count'] >= 5)
Example Use Cases
- Literature Review: Comprehensive search across STXBP1 research
- RAG Systems: Build retrieval-augmented generation for rare disease Q&A
- Research Trends: Analyze publication patterns over time
- Fine-tuning: Train domain-specific language models
- Knowledge Graphs: Extract relationships between genes, symptoms, treatments
Limitations and Known Issues
What This Dataset Contains
- ✅ Full article text where available from PMC
- ✅ Structured metadata (authors, dates, journals, DOIs)
- ✅ Abstract for all articles
- ✅ Keyword counts for relevance filtering
What This Dataset Does NOT Contain
- ❌ Images/Figures: Figure captions are included but not the actual images
- ❌ Structured Tables: Tables are converted to linear text, not preserved as structured data
- ❌ Mathematical Equations: LaTeX/MathJax equations are flattened to text
- ❌ Supplementary Materials: Links to supplements may be present but files are not included
- ❌ Section Demarcation: Text is continuous; sections (Introduction, Methods, etc.) are not tagged
Relevance Notes
- This dataset was collected using broad search terms to capture related research
- Some articles may be tangentially related (e.g., general epilepsy research, synaptic biology)
- Use the
stxbp1_countandmunc18_countfields to filter for directly relevant articles - Articles with
stxbp1_count = 0andmunc18_count = 0may still be relevant to the broader research context
Ethical Considerations
- All articles are from the PMC Open Access Subset and are available under various open licenses
- This dataset is intended for research and educational purposes
- Users should cite original articles when using specific findings
- This dataset should not be used as a substitute for professional medical advice
Citation
If you use this dataset, please cite:
@dataset{stxbp1_pubmed_fulltext_2025,
title={STXBP1 PubMed Central Full-Text Dataset},
author={[Adam Freygang]},
year={2025},
publisher={Hugging Face},
url={https://huggingface.co/datasets/SkyWhal3/stxbp1-pubmed-fulltext}
}
Acknowledgments
This dataset was curated by a parent advocate in the STXBP1 community to accelerate research into treatments and potential cures for STXBP1-related disorders.
Special thanks to:
- The researchers whose work is represented in this dataset
- PubMed Central for providing open access to scientific literature
- The STXBP1 Foundation and patient advocacy community
- Anthropic Claude Code
Version History
| Version | Date | Changes |
|---|---|---|
| 1.0.0 | 12-07-2025 | Initial release |
Contact
For questions, corrections, or contributions, please open an issue on this repository.
This dataset is dedicated to all children and families affected by STXBP1 Encephalopathy.
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