Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_provenance.
- befree-2016 importedOn "2016-02-19" NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_provenance.
- NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_assertion wasGeneratedBy ECO_0000203 NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_provenance.
- NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_assertion wasDerivedFrom befree-2016 NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_provenance.
- NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_assertion SIO_000772 19641190 NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_provenance.
- NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_assertion evidence source_evidence_literature NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_provenance.
- NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_assertion description "[We report 2 novel, cryptic chromosomal abnormalities in precursor B-cell acute lymphoblastic leukemia (BCP-ALL): a translocation, either t(X;14)(p22;q32) or t(Y;14)(p11;q32), in 33 patients and an interstitial deletion, either del(X)(p22.33p22.33) or del(Y)(p11.32p11.32), in 64 patients, involving the pseudoautosomal region (PAR1) of the sex chromosomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754269.RAC7N8IEHwPWI5hslrcBHQXeyN2hcL3UIZlI6cU4r3Vlk130_provenance.