Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_provenance.
- NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_assertion description "[To comprehensively assess the contribution of BCL11B inactivation to human T-ALL, we performed DNA copy number and sequencing analyses of T-ALL diagnostic specimens, revealing monoallelic BCL11B deletions or missense mutations in 9% (n = 10 of 117) of cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_provenance.
- NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_assertion evidence source_evidence_literature NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_provenance.
- NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_assertion SIO_000772 21878675 NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_provenance.
- NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_assertion wasDerivedFrom befree-20140225 NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_provenance.
- NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_assertion wasGeneratedBy ECO_0000203 NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP650791.RAjsxNgJ1qI5aGGC4wMumaQIM3rF9mXIoX4XMvu_QYlMM130_provenance.