Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_provenance.
- NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_assertion description "[The remaining cases usually lack the JAK2(V617F)mutation, have a platelet count less than 600 � 10(3)/?L (600 � 10(9)/L), and may represent an MDS or MPN with thrombocytosis of unknown mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_provenance.
- NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_assertion evidence source_evidence_literature NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_provenance.
- NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_assertion SIO_000772 21350094 NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_provenance.
- NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_assertion wasDerivedFrom befree-2016 NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_provenance.
- NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_assertion wasGeneratedBy ECO_0000203 NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_provenance.
- befree-2016 importedOn "2016-02-19" NP875059.RAAsUvcw4wFmLX4hJR_xPVJI2iSu23WuXqdEleWsbr5vs130_provenance.