wzkariampuzha commited on
Commit
44803cb
1 Parent(s): bda3587

Update app.py

Browse files
Files changed (1) hide show
  1. app.py +3 -2
app.py CHANGED
@@ -16,7 +16,7 @@ st.markdown('''<img src="https://huggingface.co/spaces/ncats/EpiPipeline4GARD/re
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  #st.markdown("![National Center for Advancing Translational Sciences (NCATS) Logo](https://huggingface.co/spaces/ncats/EpiPipeline4GARD/resolve/main/NCATS_logo.png")
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  #st.markdown('''<img src="https://huggingface.co/spaces/ncats/EpiPipeline4GARD/raw/main/NCATS_logo.svg" alt="National Center for Advancing Translational Sciences Logo" width="800" height="300">''',unsafe_allow_html=True)
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  st.title("Epidemiology Extraction Pipeline for Rare Diseases")
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- st.subheader("National Center for Advancing Translational Sciences (NIH/NCATS)")
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  #### CHANGE SIDEBAR WIDTH ###
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  st.markdown(
@@ -72,7 +72,8 @@ with st.spinner('Loading Epidemiology Models and Dependencies...'):
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  #classify_model_vars = (nlp, nlpSci, nlpSci2, classify_model, classify_tokenizer)
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  st.success('All Models and Dependencies Loaded!')
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- disease_or_gard_id = st.text_input("Input a rare disease term or GARD ID.")
 
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  if disease_or_gard_id:
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  df = extract_abs.streamlit_extraction(disease_or_gard_id, max_results, filtering,
 
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  #st.markdown("![National Center for Advancing Translational Sciences (NCATS) Logo](https://huggingface.co/spaces/ncats/EpiPipeline4GARD/resolve/main/NCATS_logo.png")
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  #st.markdown('''<img src="https://huggingface.co/spaces/ncats/EpiPipeline4GARD/raw/main/NCATS_logo.svg" alt="National Center for Advancing Translational Sciences Logo" width="800" height="300">''',unsafe_allow_html=True)
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  st.title("Epidemiology Extraction Pipeline for Rare Diseases")
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+ #st.subheader("National Center for Advancing Translational Sciences (NIH/NCATS)")
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  #### CHANGE SIDEBAR WIDTH ###
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  st.markdown(
 
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  #classify_model_vars = (nlp, nlpSci, nlpSci2, classify_model, classify_tokenizer)
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  st.success('All Models and Dependencies Loaded!')
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+ disease_or_gard_id = st.text_input("Input a rare disease term or GARD ID such as Fellman syndrome, Classic Homocystinuria, phenylketonuria, GARD:000941")
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+ st.markdown("A full list of rare diseases tracked by GARD can be found [here](https://rarediseases.info.nih.gov/diseases/browse-by-first-letter)")
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  if disease_or_gard_id:
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  df = extract_abs.streamlit_extraction(disease_or_gard_id, max_results, filtering,