Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_provenance.
- befree-2016 importedOn "2016-02-19" NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_provenance.
- NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_assertion wasGeneratedBy ECO_0000203 NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_provenance.
- NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_assertion wasDerivedFrom befree-2016 NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_provenance.
- NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_assertion SIO_000772 20966544 NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_provenance.
- NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_assertion evidence source_evidence_literature NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_provenance.
- NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_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." NP847399.RAonz2fmzmI0bJgmQwB9iJG7JQFOLKx1j_BYK7gWxfj88130_provenance.