Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_assertion> ?p ?o ?g. }
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- NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_assertion type Assertion NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_head.
- NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_assertion wasGeneratedBy ECO_0000203 NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_provenance.
- NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_assertion wasDerivedFrom befree-20140225 NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_provenance.
- NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_assertion SIO_000772 12907366 NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_provenance.
- NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_assertion evidence source_evidence_literature NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_provenance.
- NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_assertion description "[Rare cases of MLS show a variant t(12;22) translocation, resulting in EWS-CHOP fusion gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_provenance.