Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_provenance.
- NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_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." NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_provenance.
- NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_assertion evidence source_evidence_literature NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_provenance.
- NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_assertion SIO_000772 16386788 NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_provenance.
- NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_assertion wasDerivedFrom befree-20140225 NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_provenance.
- NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_assertion wasGeneratedBy ECO_0000203 NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP190650.RAzS2UnGtr5UT06n3WrBac10HFpq2WFAX7Vb4mCxiblMs130_provenance.