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- source_evidence_literature type ECO_0000212 NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_provenance.
- NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_assertion description "[High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_provenance.
- NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_assertion evidence source_evidence_literature NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_provenance.
- NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_assertion SIO_000772 16646086 NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_provenance.
- NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_assertion wasDerivedFrom befree-2016 NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_provenance.
- NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_assertion wasGeneratedBy ECO_0000203 NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_provenance.
- befree-2016 importedOn "2016-02-19" NP547379.RAgzgclKGTkzfpZpOwbPxjVgEDnznE5NkveK2-Fo2M300130_provenance.