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- source_evidence_literature type ECO_0000212 NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_provenance.
- NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_assertion description "[Finally, we also tested for this TFR2 mutation 20 H63D homozygotes with milder manifestations of iron overload and no acquired cause of iron overload.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_provenance.
- NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_assertion evidence source_evidence_literature NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_provenance.
- NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_assertion SIO_000772 11358390 NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_provenance.
- NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_assertion wasDerivedFrom befree-20140225 NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_provenance.
- NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_assertion wasGeneratedBy ECO_0000203 NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP315434.RA38GNwUvJwMk6NdcUQR3k_U_J93de2F6jZLG-8yJyU0Y130_provenance.