Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_provenance.
- NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_assertion description "[In order to determine whether these genes are more widely involved in haematological malignancies, we have investigated a total of 84 samples that did not have homozygous p16 or p15 deletions from patients with acute lymphoid leukaemia (n=13), acute myeloid leukaemia (n=24) and chronic myeloid leukaemia in blast crisis (n=43) as well as four haemopoietic cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_provenance.
- NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_assertion evidence source_evidence_literature NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_provenance.
- NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_assertion SIO_000772 8616035 NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_provenance.
- NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_assertion wasDerivedFrom befree-20150227 NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_provenance.
- NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_assertion wasGeneratedBy ECO_0000203 NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP847608.RAbrt4e1O3nNLm4tDuPgHsNYXeJRieTLLGAxeoxTRMUmM130_provenance.