Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_assertion type Assertion NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_head.
- NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_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." NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance.
- NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_assertion evidence source_evidence_literature NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance.
- NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_assertion SIO_000772 9054934 NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance.
- NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_assertion wasDerivedFrom befree-20140225 NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance.
- NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_assertion wasGeneratedBy ECO_0000203 NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance.