Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance.