Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_provenance.
- NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_assertion description "[The variable region of the IgH gene of secondary DLBCL (CD5+ two cases and CD5- two cases) exhibited a 0.5-9.0% somatic mutation range and no intraclonal microheterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_provenance.
- NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_assertion evidence source_evidence_literature NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_provenance.
- NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_assertion SIO_000772 10972862 NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_provenance.
- NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_assertion wasDerivedFrom befree-2016 NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_provenance.
- NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_assertion wasGeneratedBy ECO_0000203 NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_provenance.
- befree-2016 importedOn "2016-02-19" NP294074.RAylm5PdA5vx2WrIgvJ5whXG7zvjnsNbsZvqu1GCKpPgI130_provenance.