Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_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.
- NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_assertion evidence source_evidence_literature NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_provenance.
- NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_assertion SIO_000772 18024388 NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_provenance.
- NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_assertion wasDerivedFrom befree-20150227 NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_provenance.
- NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_assertion wasGeneratedBy ECO_0000203 NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP519526.RAfC9qNm_-l0ZPzd6Diuac3dub0bmlW1Lr06SKi5XuY2U130_provenance.