Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_provenance.
- NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_assertion wasGeneratedBy ECO_0000203 NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_provenance.
- NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_assertion wasDerivedFrom befree-20150227 NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_provenance.
- NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_assertion SIO_000772 20966544 NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_provenance.
- NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_assertion evidence source_evidence_literature NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_provenance.
- NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_assertion description "[Recently, a single gain-of-function point mutation of JAK2 was described in myeloproliferative diseases leading to constitutive Jak2 kinase activity, subsequent Stat5a/b activation and involvement of V617F Jak2 in the pathogenesis of myeloproliferative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717573.RAGqL9mcy2IlVMEfHpBe_r224fOTZ5kTW8sWW8JfxYSUw130_provenance.