Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance.
- NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_assertion description "[The JAK2 V617F point mutation is very rare in hypereosinophilic syndrome and/or chronic eosinophilic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance.
- NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_assertion evidence source_evidence_literature NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance.
- NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_assertion SIO_000772 18024388 NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance.
- NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_assertion wasDerivedFrom befree-20140225 NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance.
- NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_assertion wasGeneratedBy ECO_0000203 NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance.