Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_assertion type Assertion NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_head.
- NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_assertion wasGeneratedBy ECO_0000203 NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_provenance.
- NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_assertion wasDerivedFrom befree-20140225 NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_provenance.
- NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_assertion SIO_000772 19339306 NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_provenance.
- NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_assertion evidence source_evidence_literature NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_provenance.
- NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_provenance.