Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_provenance.
- NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_assertion description "[Pericentric inversion of chromosome 16 and translocation t(16;16) resulting in chimeric fusion of CBFB and MYH11 genes are typically seen in the M4-Eo FAB classification subset of AML and are associated with low-risk disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_provenance.
- NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_assertion evidence source_evidence_literature NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_provenance.
- NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_assertion SIO_000772 10800163 NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_provenance.
- NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_assertion wasDerivedFrom befree-2016 NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_provenance.
- NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_assertion wasGeneratedBy ECO_0000203 NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_provenance.
- befree-2016 importedOn "2016-02-19" NP283169.RAdni1GScOJkdclppTaBorKvwcQhA13nQrjPZ_pFlx1f8130_provenance.