Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_assertion> ?p ?o ?g. }
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- NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_assertion type Assertion NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_head.
- NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_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." NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_provenance.
- NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_assertion evidence source_evidence_literature NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_provenance.
- NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_assertion SIO_000772 21761433 NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_provenance.
- NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_assertion wasDerivedFrom befree-20140225 NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_provenance.
- NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_assertion wasGeneratedBy ECO_0000203 NP824372.RAn-pQacSoVre9rgjp8UqbcCDtSCUsUc0ORXU8ntc8aRs130_provenance.