Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance.
- NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance.
- NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_assertion evidence source_evidence_literature NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance.
- NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_assertion SIO_000772 23415222 NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance.
- NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_assertion wasDerivedFrom befree-2016 NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance.
- NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_assertion wasGeneratedBy ECO_0000203 NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance.