Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_assertion> ?p ?o ?g. }
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- NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_assertion type Assertion NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_head.
- NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_assertion wasGeneratedBy ECO_0000203 NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_provenance.
- NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_assertion wasDerivedFrom befree-2016 NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_provenance.
- NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_assertion SIO_000772 20357205 NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_provenance.
- NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_assertion evidence source_evidence_literature NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_provenance.
- NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_assertion description "[Common mutations for Leber's hereditary optic neuropathy (LHON: G11778A; T14484C; and G3460A) were not present in AMD samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP803531.RAx1dNqxryY39kaz17Ep0dsHZBfWJ_AP8GafiYyE7E9UM130_provenance.