Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_provenance.
- NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_assertion description "[The other 9 mutations were only apparent in the AML cells and affected known AML-associated genes (RUNX1 and ASXL1) and chromatin remodelers (SUZ12 and EP300).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_provenance.
- NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_assertion evidence source_evidence_literature NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_provenance.
- NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_assertion SIO_000772 22371884 NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_provenance.
- NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_assertion wasDerivedFrom befree-2016 NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_provenance.
- NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_assertion wasGeneratedBy ECO_0000203 NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_provenance.
- befree-2016 importedOn "2016-02-19" NP964008.RAr9C478-ncH2DTEXEMXenVit4E-_ojAT8pyzS3M3TnWM130_provenance.