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- source_evidence_literature type ECO_0000212 NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_provenance.
- NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_assertion description "[The new findings of importance are the following: (1) this congenital disorder is a slowly progressive abiotrophy, with progressive macular scarring and cone dysfunction, rather than a stationary anomaly; (2) carrier females sometimes can be found by ophthalmoscopic and fluorescein angiographic abnormalities in the macula; and (3) genetic linkage studies give evidence against linkage with the locus for the Xg blood group, but they suggest possible linkage with the glucose-6-phosphate dehydrogenase locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_provenance.
- NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_assertion evidence source_evidence_literature NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_provenance.
- NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_assertion SIO_000772 6971088 NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_provenance.
- NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_assertion wasDerivedFrom befree-20150227 NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_provenance.
- NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_assertion wasGeneratedBy ECO_0000203 NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_provenance.