Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_provenance.
- NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_assertion description "[A single point mutation (Val617Phe) was identified in JAK2 in 71 (97%) of 73 patients with polycythaemia vera, 29 (57%) of 51 with essential thrombocythaemia, and eight (50%) of 16 with idiopathic myelofibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_provenance.
- NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_assertion evidence source_evidence_curated NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_provenance.
- NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_assertion SIO_000772 15781101 NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_provenance.
- NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_assertion wasDerivedFrom ctd_human-20150221 NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_provenance.
- NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_assertion wasGeneratedBy ECO_0000218 NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP19961.RAGbPC1_99y-FmJQwgocRiX68w8dSl0s2J4InOVHS18sQ130_provenance.