Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_assertion> ?p ?o ?g. }
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- NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_assertion type Assertion NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_head.
- 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.