Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_provenance.
- NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_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." NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_provenance.
- NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_assertion evidence source_evidence_literature NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_provenance.
- NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_assertion SIO_000772 10634644 NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_provenance.
- NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_assertion wasDerivedFrom befree-2016 NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_provenance.
- NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_assertion wasGeneratedBy ECO_0000203 NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_provenance.
- befree-2016 importedOn "2016-02-19" NP272488.RAHv5Q2OgidINWO97NkHYB-jP4hN-H3xl6PFnwYHyydiA130_provenance.