Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_provenance.
- NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_assertion description "[The t(6;9)(p23;q34) is a recurrent chromosomal abnormality observed in 1% of acute myelogenous leukemia (AML), which generates a fusion transcript between DEK and CAN/NUP214 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_provenance.
- NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_assertion evidence source_evidence_literature NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_provenance.
- NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_assertion SIO_000772 15973457 NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_provenance.
- NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_assertion wasDerivedFrom befree-2016 NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_provenance.
- NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_assertion wasGeneratedBy ECO_0000203 NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_provenance.
- befree-2016 importedOn "2016-02-19" NP500674.RAaNKzO_PdgbA55tHaQrSHlK2VF-TakgMD8QqutPN-AFI130_provenance.