Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_provenance.
- NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_assertion description "[New recurrent changes were identified, ie, monosomies 7 present in Ph-ALL (17%) and also in other ALL (8%) and two new recurrent translocations, t(1;11)(p34;pll) in T-ALL and t(1;7)(q11-21;q35-36) in Ph+ ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_provenance.
- NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_assertion evidence source_evidence_literature NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_provenance.
- NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_assertion SIO_000772 8605327 NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_provenance.
- NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_assertion wasDerivedFrom befree-20140225 NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_provenance.
- NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_assertion wasGeneratedBy ECO_0000203 NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718871.RAaHogGGlCISayOaAIFMctCMqcl6tXEhtZYpC_Zo0BRyc130_provenance.