Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_provenance.
- NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_assertion description "[Variant t(2;11)(p11;q13) associated with the IgK-CCND1 rearrangement is a recurrent translocation in leukemic small-cell B-non-Hodgkin lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_provenance.
- NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_assertion evidence source_evidence_literature NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_provenance.
- NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_assertion SIO_000772 15306823 NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_provenance.
- NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_assertion wasDerivedFrom befree-2016 NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_provenance.
- NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_assertion wasGeneratedBy ECO_0000203 NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_provenance.
- befree-2016 importedOn "2016-02-19" NP455629.RArk7WvdqKZPbs0bLLvyBNM_rvfEjkRUhykK7nVKDApgo130_provenance.