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- source_evidence_literature type ECO_0000212 NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_provenance.
- NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_assertion description "[Taken together, our data identify distinct mechanisms underlying ectopic MEF2C expression in T-ALL, either as a downstream target of NKX2-5, or via chromosomal aberrations deleting proximal gene regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_provenance.
- NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_assertion evidence source_evidence_literature NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_provenance.
- NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_assertion SIO_000772 18079734 NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_provenance.
- NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_assertion wasDerivedFrom befree-20150227 NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_provenance.
- NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_assertion wasGeneratedBy ECO_0000203 NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333981.RAHhnoB_oNBUVs7OVHLPDF0-SlQ9Zag424-NiqOrQRCMQ130_provenance.