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- NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_assertion type Assertion NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_head.
- NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_assertion description "[Some features of GPS[+] overlap with Stargardt disease (STGD1), a recessive macular dystrophy caused by biallelic sequence variants in the ATP-binding cassette transporter 4 (ABCA4) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_provenance.
- NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_assertion evidence source_evidence_literature NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_provenance.
- NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_assertion SIO_000772 22427542 NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_provenance.
- NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_assertion wasDerivedFrom befree-2016 NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_provenance.
- NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_assertion wasGeneratedBy ECO_0000203 NP968619.RA7U0F1LuNkgHVOCyGJAmHb1S0lUnzHhurL-Jqj9bcbk0130_provenance.