Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_provenance.
- NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_assertion description "[These observations signify immediate clinical relevance and warrant i) CALR and ASXL1 mutation determination in all patients with PMF and ii) molecular revision of DIPSS-plus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_provenance.
- NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_assertion evidence source_evidence_literature NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_provenance.
- NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_assertion SIO_000772 24496303 NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_provenance.
- NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_assertion wasDerivedFrom befree-2016 NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_provenance.
- NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_assertion wasGeneratedBy ECO_0000203 NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1152065.RAdZHeQkXgQlprv4FsII8bWN7g2MlJplsqsP5d-H-jgO0130_provenance.