Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_provenance.
- NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_assertion description "[To describe three siblings with childhood cone-rod dystrophy and macular cystic degeneration in a family with apparently variable phenotypes of CRB1-related recessive retinal dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_provenance.
- NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_assertion evidence source_evidence_literature NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_provenance.
- NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_assertion SIO_000772 23767994 NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_provenance.
- NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_assertion wasDerivedFrom befree-2016 NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_provenance.
- NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_assertion wasGeneratedBy ECO_0000203 NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1086033.RAeVSEVfh15wFKCZiVXuUAqk8xxb6VCm4l6P2YfXqYUKU130_provenance.