Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_provenance.
- NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_assertion description "[The mutation is also frequently detected in core-binding factor acute myeloid leukemia (CBF AML) defined by the presence of t(8;21)(q22;q22); RUNX1-RUNX1T1 or inv(16)(p13.1;q22)/t(16;16)(p13.1;q22); CBFB-MYH11 chromosomal rearrangements, but whether the mutation is indicative of associated SM is unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_provenance.
- NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_assertion evidence source_evidence_literature NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_provenance.
- NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_assertion SIO_000772 22145956 NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_provenance.
- NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_assertion wasDerivedFrom befree-20150227 NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_provenance.
- NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_assertion wasGeneratedBy ECO_0000203 NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285500.RAUEksMMo1MMud1h_LoDSB-0eE5exkf3S0LSGoCkmMDWY130_provenance.