Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_provenance>. }
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- source_evidence_predicted type ECO_0000266 NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_provenance.
- source_evidence_predicted label "DisGeNET evidence - PREDICTED" NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_provenance.
- source_evidence_predicted comment "Gene-disease associations inferred from animal model manually asserted gene-disease associations." NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_provenance.
- NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_assertion description "[Identification of the mouse and rat orthologs of the gene mutated in Usher syndrome type IIA and the cellular source of USH2A mRNA in retina, a target tissue of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_provenance.
- NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_assertion evidence source_evidence_predicted NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_provenance.
- NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_assertion SIO_000772 12160733 NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_provenance.
- NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_assertion wasDerivedFrom rgd-20130729 NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_provenance.
- NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_assertion wasGeneratedBy ECO_0000218 NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_provenance.
- rgd-20130729 importedOn "2013-07-29" NP40549.RADQRupr6VGtfLIfdM9h0kgDWUPYSEYF9bCyrEvczI4v8130_provenance.