Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_provenance.
- NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_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." NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_provenance.
- NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_assertion evidence source_evidence_literature NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_provenance.
- NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_assertion SIO_000772 22162288 NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_provenance.
- NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_assertion wasDerivedFrom befree-20140225 NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_provenance.
- NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_assertion wasGeneratedBy ECO_0000203 NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP503498.RAIJX79i1s0Ojg4mj8mVU5nhaVtGJ-hyN51i0hc2wu9V8130_provenance.