Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_assertion> ?p ?o ?g. }
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- NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_assertion type Assertion NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_head.
- NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_assertion description "[Idiopathic hypereosinophilic syndrome (HES) characterized by unexplained and persistent hypereosinophilia is heterogeneous and comprises several entities: a myeloproliferative form where myeloid lineages are involved with the interstitial chromosome 4q12 deletion leading to fusion between FIP1L1 and PDGFRA genes, the latter acquiring increased tyrosine kinase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_provenance.
- NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_assertion evidence source_evidence_literature NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_provenance.
- NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_assertion SIO_000772 15772698 NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_provenance.
- NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_assertion wasDerivedFrom befree-20140225 NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_provenance.
- NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_assertion wasGeneratedBy ECO_0000203 NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_provenance.