Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_provenance.
- NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_assertion description "[In 4 CLL cases with unmutated VH genes, a common minimal 3.5-Mb gain of 2p16 spanning the REL and BCL11A oncogenes was identified, implicating these genes in the pathogenesis of CLL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_provenance.
- NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_assertion evidence source_evidence_literature NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_provenance.
- NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_assertion SIO_000772 17053054 NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_provenance.
- NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_assertion wasDerivedFrom befree-2016 NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_provenance.
- NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_assertion wasGeneratedBy ECO_0000203 NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_provenance.
- befree-2016 importedOn "2016-02-19" NP575344.RAvWvi8t36spmcWmB5t2c81vE6PsA1tizxfeNYCLCeMKE130_provenance.