Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_assertion type Assertion NP705306.RAYG12KtuZoQ0_gJYuMhO62WYbaZKUFfdi9W1nT-QBTDg130_head.
- 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.