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- NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_assertion type Assertion NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_head.
- NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_assertion description "[To review three inherited retinal disorders associated with diagnostic or pathognomonic electroretinogram (ERG) abnormalities: cone dystrophy with supernormal rod ERG (KCNV2), enhanced S-cone syndrome (NR2E3), and bradyopsia (RGS9/R9AP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_provenance.
- NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_assertion evidence source_evidence_literature NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_provenance.
- NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_assertion SIO_000772 23263253 NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_provenance.
- NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_assertion wasDerivedFrom befree-20140225 NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_provenance.
- NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_assertion wasGeneratedBy ECO_0000203 NP519805.RAsAai4EXIkY6EE8mWN74NaLrFR7Bk7gfAYws_w2WyCLo130_provenance.