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- source_evidence_literature type ECO_0000212 NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_provenance.
- NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_assertion description "[Though RT-PCR is highly sensitive in detecting CBFB/MYH11 fusion transcripts during remission, monitoring of minimal residual disease in patients with inv(16) remains to be established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_provenance.
- NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_assertion evidence source_evidence_literature NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_provenance.
- NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_assertion SIO_000772 7577615 NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_provenance.
- NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_assertion wasDerivedFrom befree-20140225 NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_provenance.
- NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_assertion wasGeneratedBy ECO_0000203 NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_provenance.
- befree-20140225 importedOn "2014-02-25" NP395078.RAdPRkae9hHXuwMCA2hEZG5xWed-Z2iSDX13cc5GeFQ10130_provenance.