Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_provenance.
- NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_assertion description "[Abnormality of the MLL gene located on chromosome 11q23 has been well known in therapy-related myeloid malignancies, but it has been reported only recently that the inv(11)(p15q22) in de novo or therapy-related myeloid malignancies results in the fusion of NUP98 on chromosome 11p15 and DDX10 on chromosome 11q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_provenance.
- NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_assertion evidence source_evidence_literature NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_provenance.
- NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_assertion SIO_000772 10222653 NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_provenance.
- NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_assertion wasDerivedFrom befree-20140225 NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_provenance.
- NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_assertion wasGeneratedBy ECO_0000203 NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP246465.RAIoo7pnvTLcvEUXV5px_5F8nIHEi5N-uYKq91VDsxXTk130_provenance.