Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_provenance.
- NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_assertion description "[NUP98-HOXD13 (NHD13) fusions have been identified in patients with myelodysplastic syndrome, acute myelogenous leukemia and chronic myeloid leukemia blast crisis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_provenance.
- NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_assertion evidence source_evidence_literature NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_provenance.
- NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_assertion SIO_000772 17377591 NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_provenance.
- NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_assertion wasDerivedFrom befree-2016 NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_provenance.
- NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_assertion wasGeneratedBy ECO_0000203 NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_provenance.
- befree-2016 importedOn "2016-02-19" NP600405.RAEpwFoqP5P4rxatx0mfasXxl3vaKHtYH7OTY_Xpa1r_A130_provenance.