Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_assertion> ?p ?o ?g. }
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- NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_assertion type Assertion NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_head.
- NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_provenance.
- NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_assertion evidence source_evidence_literature NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_provenance.
- NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_assertion SIO_000772 9054934 NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_provenance.
- NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_assertion wasDerivedFrom befree-2016 NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_provenance.
- NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_assertion wasGeneratedBy ECO_0000203 NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_provenance.