Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_provenance.
- NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_assertion description "[The ETV6-RUNX1 fusion is the molecular consequence of the t(12;21)(p13;q22) seen in approximately 25% of children with acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_provenance.
- NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_assertion evidence source_evidence_literature NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_provenance.
- NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_assertion SIO_000772 18767146 NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_provenance.
- NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_assertion wasDerivedFrom befree-2016 NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_provenance.
- NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_assertion wasGeneratedBy ECO_0000203 NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_provenance.
- befree-2016 importedOn "2016-02-19" NP691250.RABM-9w9sq721NSKcaAbXoGFOQ5gBvFXlIaLwjl84ish4130_provenance.