Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_provenance.
- NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_assertion description "[Patients with FAB M0 and M7 AML (no MPO expression) or M3 AML (100% MPO expression) and Down's syndrome were excluded.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_provenance.
- NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_assertion evidence source_evidence_literature NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_provenance.
- NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_assertion SIO_000772 17763467 NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_provenance.
- NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_assertion wasDerivedFrom befree-2016 NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_provenance.
- NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_assertion wasGeneratedBy ECO_0000203 NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_provenance.
- befree-2016 importedOn "2016-02-19" NP627698.RAKDGW9IPPEO6gcABeey2yY7uX7y8EeYl68RfHyNx7zlA130_provenance.