Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_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." NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_provenance.
- 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." provenance.
- 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." provenance.
- 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." provenance.
- NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_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." NP691783.RAENIsGN5dWmRo3B8gi06ByEXOQ35hWp2DOfdWqlzRkF0130_provenance.
- 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.
- 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.
- NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_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." NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_provenance.
- NP641075.RAyQ0DkFDrh8TGn9hl3oRoch6JFJZPCgleDX-5mgLdgvQ130_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." NP641075.RAyQ0DkFDrh8TGn9hl3oRoch6JFJZPCgleDX-5mgLdgvQ130_provenance.