Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_assertion> ?p ?o ?g. }
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- NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_assertion type Assertion NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_head.
- NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_assertion description "[Simultaneously, novel somatic mutations in SETBP1 were found to be enriched in CNL with possible prognostic significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_provenance.
- NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_assertion evidence source_evidence_literature NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_provenance.
- NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_assertion SIO_000772 24335708 NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_provenance.
- NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_assertion wasDerivedFrom befree-20150227 NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_provenance.
- NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_assertion wasGeneratedBy ECO_0000203 NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_provenance.