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- source_evidence_literature type ECO_0000212 NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP881221.RAUpoWS3vMTHSgQyhhwIU7fmBggmb3S-0PfyjqpqhPfxE130_provenance.