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- source_evidence_literature type ECO_0000212 NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance.
- NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_assertion description "[The high prevalence of the V617F mutation of Janus kinase 2 and associated mutations in myeloproliferative disorders (> 95% in polycythemia vera and about half of patients with essential thrombocythemia and primary myelofibrosis) has led the World Health Organization to alter the diagnostic criteria for these myeloproliferative disorders, and these changes are reviewed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance.
- NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_assertion evidence source_evidence_literature NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance.
- NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_assertion SIO_000772 18300758 NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance.
- NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_assertion wasDerivedFrom befree-2016 NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance.
- NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_assertion wasGeneratedBy ECO_0000203 NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance.
- befree-2016 importedOn "2016-02-19" NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance.