Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_provenance.
- NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_assertion description "[The presence of a modifying-sequence change in the coding region of ROM1 for two people with retinitis pigmentosa from two families with intrafamilial variation in RDS mutation phenotype has been excluded in this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_provenance.
- NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_assertion evidence source_evidence_literature NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_provenance.
- NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_assertion SIO_000772 16916875 NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_provenance.
- NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_assertion wasDerivedFrom befree-20140225 NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_provenance.
- NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_assertion wasGeneratedBy ECO_0000203 NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP226578.RA0BYs0phJsUvcLwjoTboVXdIeD-FL9nte6sxNmbuZ8oY130_provenance.