Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_provenance.
- NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_assertion description "[The t(8;21) RUNX1-ETO translocation is one of the most frequent cytogenetic abnormalities in acute myeloid leukemia (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_provenance.
- NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_assertion evidence source_evidence_literature NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_provenance.
- NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_assertion SIO_000772 21937700 NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_provenance.
- NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_assertion wasDerivedFrom befree-2016 NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_provenance.
- NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_assertion wasGeneratedBy ECO_0000203 NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_provenance.
- befree-2016 importedOn "2016-02-19" NP925575.RAXK65uaQWIpD43nVipku2j2p3gqVxWjOrYZhvvp6i1Xs130_provenance.