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- source_evidence_literature type ECO_0000212 NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_provenance.
- NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_assertion description "[GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_provenance.
- NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_assertion evidence source_evidence_literature NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_provenance.
- NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_assertion SIO_000772 20201936 NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_provenance.
- NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_assertion wasDerivedFrom gad-20150221 NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_provenance.
- NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_assertion wasGeneratedBy ECO_0000203 NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP51507.RAUK2JL94PphJB_ZBWVx21DL4ywHXkxcuI53Rhl0qfDpg130_provenance.