Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance.
- NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_assertion description "[The inv(11)(p15q22), a rare but recurrent chromosome abnormality that creates a NUP98-DDX10 fusion gene, is associated with de novo or secondary myeloid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance.
- NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_assertion evidence source_evidence_literature NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance.
- NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_assertion SIO_000772 17116492 NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance.
- NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_assertion wasDerivedFrom befree-20140225 NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance.
- NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_assertion wasGeneratedBy ECO_0000203 NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_provenance.