Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_provenance.
- NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_assertion description "[Twenty-one unrelated index cases with a clinical diagnosis of LCA were screened for mutations in the coding sequence of RetGC1, RPE65 and AIPL1 gene with single strand conformation polymorphism analysis followed by direct sequencing and restriction enzyme digestion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_provenance.
- NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_assertion evidence source_evidence_literature NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_provenance.
- NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_assertion SIO_000772 14611946 NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_provenance.
- NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_assertion wasDerivedFrom befree-2016 NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_provenance.
- NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_assertion wasGeneratedBy ECO_0000203 NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_provenance.
- befree-2016 importedOn "2016-02-19" NP420138.RA5YTBUfkjqRtbOlQQ2NeBPk8kaeIVIReJU07peRNWK0M130_provenance.