Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_provenance.
- NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_assertion description "[The JAK2(V617F) mutation, which has been found in patients with myeloproliferative disorders (MPD), has not yet been evaluated in lymphoproliferative disorders by any adequately sensitive techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_provenance.
- NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_assertion evidence source_evidence_literature NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_provenance.
- NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_assertion SIO_000772 18032883 NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_provenance.
- NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_assertion wasDerivedFrom befree-2016 NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_provenance.
- NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_assertion wasGeneratedBy ECO_0000203 NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_provenance.
- befree-2016 importedOn "2016-02-19" NP641745.RADi7KxEPXKm0AjIUtg-9xvyomFy0ltdI3sA9csasLFl4130_provenance.