Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_provenance.
- NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_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." NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_provenance.
- NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_assertion evidence source_evidence_literature NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_provenance.
- NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_assertion SIO_000772 19028736 NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_provenance.
- NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_assertion wasDerivedFrom befree-2016 NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_provenance.
- NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_assertion wasGeneratedBy ECO_0000203 NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_provenance.
- befree-2016 importedOn "2016-02-19" NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_provenance.