Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP665883.RAYPc4xqZqcnmO4GHvI6wqHTV1n09YpREXGLQnHyuAU3M130_provenance.