Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_assertion type Assertion NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_head.
- NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_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." NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_provenance.
- NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_assertion evidence source_evidence_literature NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_provenance.
- NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_assertion SIO_000772 18024388 NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_provenance.
- NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_assertion wasDerivedFrom befree-20150227 NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_provenance.
- NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_assertion wasGeneratedBy ECO_0000203 NP519505.RAfSujOnweYoffosnPSuZUsmTxNRJPmTIz0zlg0o9mNnU130_provenance.