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- source_evidence_literature type ECO_0000212 NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_provenance.
- NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_assertion description "[Therefore, we have analyzed 83 children with acute B-lineage ALL (67 de novo patients and 19 relapses) by PCR analysis for clonal IgH, incomplete TCRD (Vdelta2-Ddelta3 and Ddelta2-Ddelta3) and TCRG rearrangements.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_provenance.
- NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_assertion evidence source_evidence_literature NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_provenance.
- NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_assertion SIO_000772 16386788 NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_provenance.
- NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_assertion wasDerivedFrom befree-20150227 NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_provenance.
- NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_assertion wasGeneratedBy ECO_0000203 NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1001874.RAu-52moXX2oUzDQCz90K2vyHmCR5KI3L3FV3b-Erxuhk130_provenance.