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- source_evidence_literature type ECO_0000212 NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_provenance.
- NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_assertion description "[We conclude that there are rare patients with CML who either present in blast crisis with coexistence of t(9;22) and t(8;21) with or without +8, or progress to blast crisis with acquiring RUNX1-RUNX1T1 in the BCR-ABL1 clone which may or may not be therapy related and represent a later event in a multistep pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_provenance.
- NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_assertion evidence source_evidence_literature NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_provenance.
- NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_assertion SIO_000772 21504717 NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_provenance.
- NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_assertion wasDerivedFrom befree-20150227 NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_provenance.
- NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_assertion wasGeneratedBy ECO_0000203 NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP284891.RATg1ImX7v0Ix7Rh1M7N7lPeIsbEIi-rGf5veiA24tECA130_provenance.