Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_assertion> ?p ?o ?g. }
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- NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_assertion type Assertion NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_head.
- NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_assertion description "[This assignment rules out the direct involvement of the rhodopsin gene in the known mouse mutations that produce retinal degeneration, including retinal degeneration slow (rds, chromosome 17), retinal degeneration (rd, chromosome 5), Purkinje cell degeneration (pcd, chromosome 13), and nervous (nr, chromosome 8).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_provenance.
- NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_assertion evidence source_evidence_literature NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_provenance.
- NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_assertion SIO_000772 2341153 NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_provenance.
- NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_assertion wasDerivedFrom befree-2016 NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_provenance.
- NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_assertion wasGeneratedBy ECO_0000203 NP1053207.RAOXsHRgFIDaTyGXkm6vi4crSC10NDGf64PwuGpONQ9sE130_provenance.