Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_provenance.
- NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_assertion description "[Thirdly, a striking predominance of immature Ddelta2-Ddelta3 cross-lineage recombinations was observed (seven out of 16 TCRD rearrangements; 44%), whereas more mature Vdelta2-Ddelta3 gene rearrangements occurred less frequently (six out of 16 TCRD rearrangements; 38% vs >70% in pediatric precursor-B-ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_provenance.
- NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_assertion evidence source_evidence_literature NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_provenance.
- NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_assertion SIO_000772 9665194 NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_provenance.
- NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_assertion wasDerivedFrom befree-20140225 NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_provenance.
- NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_assertion wasGeneratedBy ECO_0000203 NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP861563.RAIR5xKeU-0J7DPlE-ROHFt-8HHUvM54O-tJnEQRehR5Q130_provenance.