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- source_evidence_literature type ECO_0000212 NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_provenance.
- NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_assertion description "[After evaluation of secondary causes of eosinophilia, the 2008 World Health Organization establishes a semi-molecular classification scheme of disease subtypes including 'myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, or FGFR1', chronic eosinophilic leukemia, not otherwise specified, (CEL, NOS), lymphocyte-variant hypereosinophilia, and idiopathic hypereosinophilic syndrome (HES), which is a diagnosis of exclusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_provenance.
- NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_assertion evidence source_evidence_literature NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_provenance.
- NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_assertion SIO_000772 26486351 NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_provenance.
- NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_assertion wasDerivedFrom befree-2016 NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_provenance.
- NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_assertion wasGeneratedBy ECO_0000203 NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295107.RApAaWs4D4hMzVuwESVlefZgRD2-G4P6xluK5Sb3-Ey98130_provenance.