Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_provenance.
- NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_assertion description "[In a systematic tyrosine kinase gene exon resequencing study, 21 of 24 FLT3 exons were sequenced in samples from 53 patients with AML, 9 patients with acute lymphoblastic leukemia (ALL), and 3 patients with myelodysplasia samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_provenance.
- NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_assertion evidence source_evidence_literature NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_provenance.
- NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_assertion SIO_000772 15178581 NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_provenance.
- NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_assertion wasDerivedFrom befree-20150227 NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_provenance.
- NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_assertion wasGeneratedBy ECO_0000203 NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP408001.RATJstl21umjoRzqOhnFNvGa-J5RHyG9Nso5IZqM8fTsU130_provenance.