bigbio/tmvar_v3

Dataset

language:

3

12 commits

1 linked in READMEs

updated Oct 12, 2024

See the code

README


language:

  • en bigbio_language:
  • English license: unknown multilinguality: monolingual bigbio_license_shortname: UNKNOWN pretty_name: tmVar v3 homepage: https://www.ncbi.nlm.nih.gov/research/bionlp/Tools/tmvar/ bigbio_pubmed: True bigbio_public: True bigbio_tasks:
  • NAMED_ENTITY_RECOGNITION
  • NAMED_ENTITY_DISAMBIGUATION

Dataset Card for tmVar v3

Dataset Description

This dataset contains 500 PubMed articles manually annotated with mutation mentions of various kinds and dbsnp normalizations for each of them. In addition, it contains variant normalization options such as allele-specific identifiers from the ClinGen Allele Registry It can be used for NER tasks and NED tasks, This dataset does NOT have splits.

Citation Information

@misc{https://doi.org/10.48550/arxiv.2204.03637,
  title        = {tmVar 3.0: an improved variant concept recognition and normalization tool},
  author       = {
    Wei, Chih-Hsuan and Allot, Alexis and Riehle, Kevin and Milosavljevic,
    Aleksandar and Lu, Zhiyong
  },
  year         = 2022,
  publisher    = {arXiv},
  doi          = {10.48550/ARXIV.2204.03637},
  url          = {https://arxiv.org/abs/2204.03637},
  copyright    = {Creative Commons Attribution 4.0 International},
  keywords     = {
    Computation and Language (cs.CL), FOS: Computer and information sciences,
    FOS: Computer and information sciences
  }
}


bigbio/tmvar_v3

Dataset

language:

3

12 commits

1 linked in READMEs

updated Oct 12, 2024

See the code

README


language:

  • en bigbio_language:
  • English license: unknown multilinguality: monolingual bigbio_license_shortname: UNKNOWN pretty_name: tmVar v3 homepage: https://www.ncbi.nlm.nih.gov/research/bionlp/Tools/tmvar/ bigbio_pubmed: True bigbio_public: True bigbio_tasks:
  • NAMED_ENTITY_RECOGNITION
  • NAMED_ENTITY_DISAMBIGUATION

Dataset Card for tmVar v3

Dataset Description

This dataset contains 500 PubMed articles manually annotated with mutation mentions of various kinds and dbsnp normalizations for each of them. In addition, it contains variant normalization options such as allele-specific identifiers from the ClinGen Allele Registry It can be used for NER tasks and NED tasks, This dataset does NOT have splits.

Citation Information

@misc{https://doi.org/10.48550/arxiv.2204.03637,
  title        = {tmVar 3.0: an improved variant concept recognition and normalization tool},
  author       = {
    Wei, Chih-Hsuan and Allot, Alexis and Riehle, Kevin and Milosavljevic,
    Aleksandar and Lu, Zhiyong
  },
  year         = 2022,
  publisher    = {arXiv},
  doi          = {10.48550/ARXIV.2204.03637},
  url          = {https://arxiv.org/abs/2204.03637},
  copyright    = {Creative Commons Attribution 4.0 International},
  keywords     = {
    Computation and Language (cs.CL), FOS: Computer and information sciences,
    FOS: Computer and information sciences
  }
}