Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_provenance.
- NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_assertion description "[The FAB M0 subtype was more frequent in ETV6 rearranged de novo AML than other AML (P < 0.001); expression of CD7 and CD34 by immunophenotyping was higher in ETV6 rearranged AML compared with other subgroups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_provenance.
- NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_assertion evidence source_evidence_literature NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_provenance.
- NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_assertion SIO_000772 22162288 NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_provenance.
- NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_assertion wasDerivedFrom befree-2016 NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_provenance.
- NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_assertion wasGeneratedBy ECO_0000203 NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_provenance.
- befree-2016 importedOn "2016-02-19" NP946144.RAHKx0z9xFphSMtoTlp8S2Px17hmhNWnnQqTUsRyfYeOs130_provenance.