Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_provenance.
- NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_assertion description "[The immunoglobulin heavy chain gene (IgH gene) was analysed in four cases of B-cell Richter syndrome, in order to determine whether a secondary diffuse large B-cell lymphoma (DLBCL) could arise from the same clone as the initial B-cell chronic lymphocytic leukemia (B-CLL) and lymphoplasmacytoid lymphoma (LPL) or be a de novo event, and whether secondary DLBCL shows an intraclonal microheterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_provenance.
- NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_assertion evidence source_evidence_literature NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_provenance.
- NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_assertion SIO_000772 10972862 NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_provenance.
- NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_assertion wasDerivedFrom befree-20150227 NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_provenance.
- NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_assertion wasGeneratedBy ECO_0000203 NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP486476.RAJDQCXdZCTkelLWoNds2lVHR8Cf8P8NiQT3IH-Owt1IU130_provenance.