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- NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_assertion type Assertion NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_head.
- NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_assertion description "[Mutations in ABCR are associated with at least four inherited retinal dystrophies: Stargardt disease, Fundus Flavimaculatus, cone-rod dystrophy, and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_provenance.
- NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_assertion evidence source_evidence_literature NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_provenance.
- NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_assertion SIO_000772 10396622 NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_provenance.
- NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_assertion wasDerivedFrom befree-2016 NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_provenance.
- NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_assertion wasGeneratedBy ECO_0000203 NP256828.RAe6_4LWAVBZkIySI-hB26z0seTVislnZE56UK6ss0E68130_provenance.