Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion> ?p ?o ?g. }
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- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion type Assertion NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_head.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_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." NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion evidence source_evidence_literature NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion SIO_000772 17116492 NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion wasDerivedFrom befree-20150227 NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion wasGeneratedBy ECO_0000203 NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.