Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_provenance.
- NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_assertion description "[The finding of repeated sequences typical of switch regions suggested that this translocation occurred during heavy-chain isotype switching, resulting in progression to pre-B-cell leukemia with both the t(8;14) and the t(14;18) translocations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_provenance.
- NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_assertion evidence source_evidence_literature NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_provenance.
- NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_assertion SIO_000772 3186743 NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_provenance.
- NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_assertion wasDerivedFrom befree-2016 NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_provenance.
- NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_assertion wasGeneratedBy ECO_0000203 NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1300663.RANBCbN54XPUPI-wD80xYFueAJG1aEXL7H0ej2iEr-yC4130_provenance.