Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_assertion> ?p ?o ?g. }
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- NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_assertion type Assertion NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_head.
- NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_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." NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_provenance.
- NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_assertion evidence source_evidence_literature NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_provenance.
- NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_assertion SIO_000772 21761433 NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_provenance.
- NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_assertion wasDerivedFrom befree-20140225 NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_provenance.
- NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_assertion wasGeneratedBy ECO_0000203 NP478191.RAkafaemAMs1z7mXutf38NWopsa2vX_jaRYzC_F8rXUPI130_provenance.