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- source_evidence_literature type ECO_0000212 NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_provenance.
- NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_assertion description "[For example, mutations in the ABCR gene, (recently identified in cones as well) which codes for retinal rod-specific ABCR protein is responsible for Stargardt macular dystrophy/fundus flavimaculatus, an autosomal recessive macular dystrophy with juvenile onset, which accounts for 7% of human retinal degenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_provenance.
- NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_assertion evidence source_evidence_literature NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_provenance.
- NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_assertion SIO_000772 11556484 NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_provenance.
- NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_assertion wasDerivedFrom befree-2016 NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_provenance.
- NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_assertion wasGeneratedBy ECO_0000203 NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_provenance.
- befree-2016 importedOn "2016-02-19" NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_provenance.