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- source_evidence_literature type ECO_0000212 NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_provenance.
- NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_assertion description "[In up to 70% of patients with MDS clonal chromosome abnormalities can be identified which have a high impact on setting the correct diagnosis and estimation of prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_provenance.
- NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_assertion evidence source_evidence_literature NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_provenance.
- NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_assertion SIO_000772 24507811 NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_provenance.
- NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_assertion wasDerivedFrom befree-20150227 NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_provenance.
- NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_assertion wasGeneratedBy ECO_0000203 NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781350.RA6-2I-sApzStPo3kyimwaXPmlZkEte5M1pbUDHc7UuLo130_provenance.