Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_provenance.
- NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_assertion description "[Sixty patients with a variety of retinal disorders, including Leber's congenital amaurosis, ocular albinism, pseudoxanthoma elasticum, retinitis pigmentosa, and Stargardt's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_provenance.
- NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_assertion evidence source_evidence_literature NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_provenance.
- NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_assertion SIO_000772 20801516 NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_provenance.
- NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_assertion wasDerivedFrom gad-20150221 NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_provenance.
- NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_assertion wasGeneratedBy ECO_0000203 NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP184744.RAYi72nUH5GSJuU1jYSfXQooqYoLkTAAwhVnYldN6TuEQ130_provenance.