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- source_evidence_literature type ECO_0000212 NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_provenance.
- NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_assertion description "[A Polish three-generation family with hypokalemic periodic paralysis and a mutation in CACNA1S is investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_provenance.
- NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_assertion evidence source_evidence_literature NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_provenance.
- NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_assertion SIO_000772 18229654 NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_provenance.
- NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_assertion wasDerivedFrom lhgdn-20090331 NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_provenance.
- NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_assertion wasGeneratedBy ECO_0000203 NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP233796.RAdOZ-19yjJ6Nx9XWuJc87NLNfiSbxY7Jmf-Py2TDEXD0130_provenance.