Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_assertion> ?p ?o ?g. }
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- NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_assertion type Assertion NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_head.
- NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_provenance.
- NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_assertion evidence source_evidence_literature NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_provenance.
- NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_assertion SIO_000772 9054934 NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_provenance.
- NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_assertion wasDerivedFrom befree-20140225 NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_provenance.
- NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_assertion wasGeneratedBy ECO_0000203 NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_provenance.