Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_provenance.
- NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_assertion description "[Complex karyotypes are seen in approximately 15% of de novo MDS/AML and in up to 50% of therapy-related MDS/AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_provenance.
- NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_assertion evidence source_evidence_literature NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_provenance.
- NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_assertion SIO_000772 16142824 NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_provenance.
- NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_assertion wasDerivedFrom befree-2016 NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_provenance.
- NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_assertion wasGeneratedBy ECO_0000203 NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_provenance.
- befree-2016 importedOn "2016-02-19" NP512156.RAZLsMwyM3Lnh3ffdiTWtNHM82P9GwCc1SD22eN5yR2Q0130_provenance.