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- source_evidence_literature type ECO_0000212 NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_provenance.
- NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_assertion description "[We sequenced the translocation breakpoints of 56 patients with childhood ALL or AML harboring t(12;21), t(8;21), t(15;17), inv(16), and t(1;19), and demonstrated, with the notable exception of t(1;19), that these rearrangements are commonly detected in the neonatal blood spots (Guthrie cards) of the cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_provenance.
- NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_assertion evidence source_evidence_literature NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_provenance.
- NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_assertion SIO_000772 15967214 NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_provenance.
- NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_assertion wasDerivedFrom befree-2016 NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_provenance.
- NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_assertion wasGeneratedBy ECO_0000203 NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_provenance.
- befree-2016 importedOn "2016-02-19" NP500276.RAn8-mk1ds1ORSrCytfLEjjFCGeEh6vvgANxAz2fKlQBk130_provenance.