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- source_evidence_literature type ECO_0000212 NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_provenance.
- NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_assertion description "[Collectively, these data identify a primary disease-causing molecular defect in cone cells and suggest that RDS-associated disease in patients may be a result of this defect coupled with secondary sequellae involving RPE and choriocapillaris cell loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_provenance.
- NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_assertion evidence source_evidence_literature NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_provenance.
- NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_assertion SIO_000772 24463884 NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_provenance.
- NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_assertion wasDerivedFrom befree-20150227 NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_provenance.
- NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_assertion wasGeneratedBy ECO_0000203 NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP760984.RA9L9KmSsK-EUCoXt1a4A_g5wuHi--yoTdenKhfdJMMJk130_provenance.