Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_assertion> ?p ?o ?g. }
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- NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_assertion type Assertion NP778965.RA1-djEYZ0LqVRClqt_iJUzRDS40ybDfEB4745ZICkEIQ130_head.
- 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.