Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion> ?p ?o ?g. }
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- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion type Assertion NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_head.
- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion description "[The JAK2 V617F point mutation is very rare in hypereosinophilic syndrome and/or chronic eosinophilic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion evidence source_evidence_literature NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion SIO_000772 18024388 NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion wasDerivedFrom befree-2016 NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion wasGeneratedBy ECO_0000203 NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.