Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_assertion> ?p ?o ?g. }
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- NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_assertion type Assertion NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_head.
- NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_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." NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_provenance.
- NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_assertion evidence source_evidence_literature NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_provenance.
- NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_assertion SIO_000772 6971088 NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_provenance.
- NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_assertion wasDerivedFrom befree-20150227 NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_provenance.
- NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_assertion wasGeneratedBy ECO_0000203 NP415652.RAR942Fwy2r1lIC9FVr_DHF1t3NrKZHBQ27qPPEyxJ_3Q130_provenance.