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- NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_assertion type Assertion NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_head.
- NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_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." NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_provenance.
- NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_assertion evidence source_evidence_literature NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_provenance.
- NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_assertion SIO_000772 23263253 NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_provenance.
- NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_assertion wasDerivedFrom befree-2016 NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_provenance.
- NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_assertion wasGeneratedBy ECO_0000203 NP1038240.RAKbh5-Ynfnchpf7UmqqCFlwgYmk6B5V8Ww0oqh1LteEQ130_provenance.