Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_provenance.
- befree-2016 importedOn "2016-02-19" NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_provenance.
- NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_assertion wasGeneratedBy ECO_0000203 NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_provenance.
- NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_assertion wasDerivedFrom befree-2016 NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_provenance.
- NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_assertion SIO_000772 22689681 NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_provenance.
- NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_assertion evidence source_evidence_literature NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_provenance.
- NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_assertion description "[The most prominently up-regulated genes in patients with RUNX1-mutated cytogenetically normal acute myeloid leukemia include lymphoid regulators such as HOP homeobox (HOPX), deoxynucleotidyltransferase (DNTT, terminal) and B-cell linker (BLNK), indicating lineage infidelity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989278.RAkiL40abq_HX-I95HCLIf0-Xi2Q5fN5PiSSKo32wA8jY130_provenance.