Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_provenance.
- NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_assertion wasGeneratedBy ECO_0000203 NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_provenance.
- NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_assertion wasDerivedFrom befree-20140225 NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_provenance.
- NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_assertion SIO_000772 16505158 NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_provenance.
- NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_assertion evidence source_evidence_literature NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_provenance.
- NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_assertion description "[Clinically, CORDX3 shares some features with CSNB2 but is distinguishable from CSNB2 in that it is progressive, can begin in adulthood, has no nystagmus or hyperopic refraction, has only low grade astigmatism, and in dark adaptation lacks cone threshold and has small or no elevation of rod threshold.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP792930.RAFnJnmkviOMGECMRNvFID9lygW4_OzrTQnOp5MVQNPHc130_provenance.