Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_assertion> ?p ?o ?g. }
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- NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_assertion type Assertion NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_head.
- NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_assertion wasGeneratedBy ECO_0000203 NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_provenance.
- NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_assertion wasDerivedFrom befree-20150227 NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_provenance.
- NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_assertion SIO_000772 16708387 NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_provenance.
- NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_assertion evidence source_evidence_literature NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_provenance.
- NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_assertion description "[Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881947.RAFR5yVImYNttLfOeXqTSVJPT6HGKP0TQIt4yWdaFwMHM130_provenance.