Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_assertion> ?p ?o ?g. }
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- NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_assertion type Assertion NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_head.
- NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_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." NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_provenance.
- NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_assertion evidence source_evidence_literature NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_provenance.
- NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_assertion SIO_000772 18024388 NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_provenance.
- NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_assertion wasDerivedFrom befree-20150227 NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_provenance.
- NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_assertion wasGeneratedBy ECO_0000203 NP519733.RAroLzTcwIqx7DTU_qlrrOZn15wkFjcb5lDtYLd_fhpj8130_provenance.