Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_provenance.
- NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_assertion description "[The pericentric inversion of chromosome 16 [inv(16)(p13q22)] and t(16;16)(p13;q22) are chromosomal rearrangements frequently associated with AML FAB type M4Eo resulting in the production of a fusion gene CBFB/MYH11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_provenance.
- NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_assertion evidence source_evidence_literature NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_provenance.
- NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_assertion SIO_000772 7577615 NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_provenance.
- NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_assertion wasDerivedFrom befree-2016 NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_provenance.
- NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_assertion wasGeneratedBy ECO_0000203 NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1313281.RAOMejTaXQKSW3z8ZNnylSA-FnTXUVkhpbea3-g-o4dvw130_provenance.