Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_provenance.
- befree-2016 importedOn "2016-02-19" NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_provenance.
- NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_assertion wasGeneratedBy ECO_0000203 NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_provenance.
- NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_assertion wasDerivedFrom befree-2016 NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_provenance.
- NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_assertion SIO_000772 18285826 NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_provenance.
- NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_assertion evidence source_evidence_literature NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_provenance.
- NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_assertion description "[Based on these data we estimate a prevalence of 31% for ABCA4 mutations in arCD and arCRD, supporting the concept that the ABCA4 gene is a major locus for various types of degenerative retinal diseases with abnormalities in cone or both cone and rod function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656323.RAe7wVGg9Bz7agqWXbCO2vf4u4lisK4WfYFiWgfeeuzWs130_provenance.