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- source_evidence_literature type ECO_0000212 NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_provenance.
- NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_assertion description "[Mutations in UBQLN2 and SIGMAR1 genes are rare in Korean patients with amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_provenance.
- NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_assertion evidence source_evidence_literature NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_provenance.
- NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_assertion SIO_000772 24684794 NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_provenance.
- NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_assertion wasDerivedFrom befree-2016 NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_provenance.
- NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_assertion wasGeneratedBy ECO_0000203 NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1168888.RAHFysM52ktfyqcFrLeA67NNLerfv8GYHJQ6O3ueduvlc130_provenance.