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- source_evidence_literature type ECO_0000212 NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion description "[Severe erythrocyte adenylate kinase deficiency due to homozygous A-->G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion evidence source_evidence_literature NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion SIO_000772 9432020 NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion wasDerivedFrom befree-20150227 NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion wasGeneratedBy ECO_0000203 NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.