Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_provenance.
- NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_assertion description "[Detection of the t(11;14)(q13;q32) without CCND1/IGH fusion in a case of acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_provenance.
- NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_assertion evidence source_evidence_literature NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_provenance.
- NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_assertion SIO_000772 19963117 NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_provenance.
- NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_assertion wasDerivedFrom befree-2016 NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_provenance.
- NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_assertion wasGeneratedBy ECO_0000203 NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_provenance.
- befree-2016 importedOn "2016-02-19" NP779635.RAK3JJTu9U1vVNI4gPnJG8R_wDQIrEKKwn70aMV2QP4vY130_provenance.