Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance.
- NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_assertion description "[Study shows that loss or reduced expression of DAPK1 underlies cases of heritable predisposition to chronic lymphocytic leukemia (CLL) and epigenetic silencing of DAPK1 by promoter methylation occurs in almost all sporadic CLL cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance.
- NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_assertion evidence source_evidence_literature NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance.
- NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_assertion SIO_000772 17540169 NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance.
- NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_assertion wasDerivedFrom lhgdn-20090331 NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance.
- NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_assertion wasGeneratedBy ECO_0000203 NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance.