Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP371794.RAVISekBlJONLB1t0U9AzVTehVpNfxZq42z9lBxmoVNKU130_provenance.