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- source_evidence_literature type ECO_0000212 NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_provenance.
- NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_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." NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_provenance.
- NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_assertion evidence source_evidence_literature NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_provenance.
- NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_assertion SIO_000772 24335708 NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_provenance.
- NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_assertion wasDerivedFrom befree-2016 NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_provenance.
- NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_assertion wasGeneratedBy ECO_0000203 NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1136501.RAtadVWmEBblJUSydUmrnP40HLQut17_BNlc0ngq5ArcI130_provenance.