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- source_evidence_literature type ECO_0000212 NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_provenance.
- NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_assertion description "[We used massively parallel sequencing to examine tumor samples collected from 87 patients with MDS before HSCT for coding mutations in 40 recurrently mutated MDS genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_provenance.
- NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_assertion evidence source_evidence_literature NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_provenance.
- NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_assertion SIO_000772 25092778 NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_provenance.
- NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_assertion wasDerivedFrom befree-20150227 NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_provenance.
- NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_assertion wasGeneratedBy ECO_0000203 NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978540.RATquv99YcMb9PA0BHOgdyd5xw5ran4rLTdf-_3WsZfpA130_provenance.