Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_provenance.
- NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_assertion description "[These results revealed the frequent methylation of p16 and p15 genes in B-ALL and AML despite a low frequency of p16 and p15 deletions and mutations in these leukemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_provenance.
- NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_assertion evidence source_evidence_literature NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_provenance.
- NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_assertion SIO_000772 10634644 NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_provenance.
- NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_assertion wasDerivedFrom befree-2016 NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_provenance.
- NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_assertion wasGeneratedBy ECO_0000203 NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_provenance.
- befree-2016 importedOn "2016-02-19" NP272485.RA2W_bmzAdhVPgIaGQf_GI_5xAgHFpLoH1zjJY_KpPE8c130_provenance.