Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_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.
- NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_assertion evidence source_evidence_literature NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_provenance.
- NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_assertion SIO_000772 18024388 NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_provenance.
- NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_assertion wasDerivedFrom befree-2016 NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_provenance.
- NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_assertion wasGeneratedBy ECO_0000203 NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_provenance.
- befree-2016 importedOn "2016-02-19" NP641074.RALTEO_dQBC0Deef-V6L0T_6uwH784G-lKVw972kb6tYg130_provenance.