Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_provenance.
- NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_assertion description "[Deletion of the short arm of chromosome 9 (9p), resulting in the loss of the p16INK4a/MTS1 gene, now called CDKN2, has been found to occur frequently in acute lymphoblastic leukemia, even in the absence of a microscopically visible deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_provenance.
- NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_assertion evidence source_evidence_literature NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_provenance.
- NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_assertion SIO_000772 9258663 NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_provenance.
- NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_assertion wasDerivedFrom befree-20140225 NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_provenance.
- NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_assertion wasGeneratedBy ECO_0000203 NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP686539.RASHl25SwS5Uio6E2yT2grF1T4jCy152esKf1wbZuBlEo130_provenance.