Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_provenance.
- NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_assertion description "[The frequency of the JAK2 V617F was 73% (85% in PV, 65% in ET, and 65% in CIMF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_provenance.
- NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_assertion evidence source_evidence_literature NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_provenance.
- NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_assertion SIO_000772 17255768 NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_provenance.
- NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_assertion wasDerivedFrom befree-2016 NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_provenance.
- NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_assertion wasGeneratedBy ECO_0000203 NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_provenance.
- befree-2016 importedOn "2016-02-19" NP590776.RA2AVQU3CHNBcNeS28iC-a_mHSN_bEGCAR3FMStGrSSG0130_provenance.