Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_provenance.
- NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_assertion description "[Common polymorphisms of NR3C1, ABCB1, glutathione-S-transferase (GST)-M1, GST-P1, GST-T1, and IL-10 genes were analyzed in 36 pediatric patients with ALL, treated according to the AIEOP-BMF ALL 2000 study protocol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_provenance.
- NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_assertion evidence source_evidence_literature NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_provenance.
- NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_assertion SIO_000772 19621425 NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_provenance.
- NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_assertion wasDerivedFrom befree-20150227 NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_provenance.
- NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_assertion wasGeneratedBy ECO_0000203 NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP960276.RAIITmjBTAQcRQhdaBUQN6mHuPVMvbEzaBZF1Zkd-uk8M130_provenance.