Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_provenance.
- NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_assertion description "[The t(6;9)(p23;q34) is a recurrent chromosomal abnormality observed in 1% of acute myelogenous leukemia (AML), which generates a fusion transcript between DEK and CAN/NUP214 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_provenance.
- NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_assertion evidence source_evidence_literature NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_provenance.
- NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_assertion SIO_000772 15973457 NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_provenance.
- NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_assertion wasDerivedFrom befree-20140225 NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_provenance.
- NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_assertion wasGeneratedBy ECO_0000203 NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP752338.RAlwi4G12mvTABpcF9Wma4nnr-owV6_0Re-vdnVZW-bB8130_provenance.