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- NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_assertion type Assertion NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_head.
- NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_assertion description "[Mutations in ABCA4 have been associated with autosomal recessive Stargardt disease (STGD), a few cases with autosomal recessive cone-rod dystrophy (arCRD) and autosomal recessive retinitis pigmentosa (arRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_provenance.
- NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_assertion evidence source_evidence_literature NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_provenance.
- NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_assertion SIO_000772 19028736 NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_provenance.
- NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_assertion wasDerivedFrom befree-20150227 NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_provenance.
- NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_assertion wasGeneratedBy ECO_0000203 NP218951.RAwk0pSayOaD97YR-5nFvytvqfZ5BR73kBmqncOjg_vJs130_provenance.