Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_assertion> ?p ?o ?g. }
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- NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_assertion type Assertion NP738768.RAYkarW10hkysArPAySK0nw9DNgR4PCkTnyoF0U5l0iy0130_head.
- 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.