Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_provenance.
- NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_assertion description "[This phenotype is induced by specific acute myeloid leukemia-associated translocations, such as t(15;17) and t(11;17), which involve an identical portion of the retinoic acid receptor alpha (RARalpha) and either the promyelocytic leukemia (PML) or promyelocytic zinc finger (PLZF) genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_provenance.
- NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_assertion evidence source_evidence_literature NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_provenance.
- NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_assertion SIO_000772 16024608 NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_provenance.
- NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_assertion wasDerivedFrom befree-20150227 NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_provenance.
- NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_assertion wasGeneratedBy ECO_0000203 NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP782826.RA0AC8ibwgGnOYJU7dSj42zzpFgm6QQ4LgZKNuB_5SRr4130_provenance.