Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_provenance.
- NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_assertion description "[Approximately 6% of paediatric patients with precursor B-cell acute lymphoblastic leukaemia (B-ALL) harbour a rearrangement involving the gene regions of PBX1 (1q23) and E2A (19p13.3) which is visualized cytogenetically either as a der(19)t(1;19)(q23;p13.3) or the less common balanced t(1;19)(q23;p13.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_provenance.
- NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_assertion evidence source_evidence_literature NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_provenance.
- NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_assertion SIO_000772 15801954 NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_provenance.
- NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_assertion wasDerivedFrom befree-20150227 NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_provenance.
- NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_assertion wasGeneratedBy ECO_0000203 NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP610687.RAsMkZUTfIq29PKu8LP1dWsnQUTN_wlEM-kl8pQzEhtqM130_provenance.