Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_provenance.
- NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_assertion description "[Therefore, we have analyzed 83 children with acute B-lineage ALL (67 de novo patients and 19 relapses) by PCR analysis for clonal IgH, incomplete TCRD (Vdelta2-Ddelta3 and Ddelta2-Ddelta3) and TCRG rearrangements.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_provenance.
- NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_assertion evidence source_evidence_literature NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_provenance.
- NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_assertion SIO_000772 16386788 NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_provenance.
- NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_assertion wasDerivedFrom befree-2016 NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_provenance.
- NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_assertion wasGeneratedBy ECO_0000203 NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_provenance.
- befree-2016 importedOn "2016-02-19" NP529042.RAs0UMcxbHTCDfUGOE1IUPvCxvi05L4r8mqZTFAXH8Tkk130_provenance.