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- source_evidence_literature type ECO_0000212 NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_provenance.
- NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_assertion description "[Mutations in ABCA4 have been associated with autosomal recessive Stargardt disease (STGD), a few cases with autosomal recessive cone-rod dystrophy (arCRD) and autosomal recessive retinitis pigmentosa (arRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_provenance.
- NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_assertion evidence source_evidence_literature NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_provenance.
- NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_assertion SIO_000772 19028736 NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_provenance.
- NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_assertion wasDerivedFrom befree-20140225 NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_provenance.
- NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_assertion wasGeneratedBy ECO_0000203 NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP792394.RA4D2Np5a9DgY4bww0l-EUMEg5JEii-lgLYRz8H1uQvZc130_provenance.