Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_provenance.
- NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_assertion description "[In this context, the distinctive role of a positive JAK2(V617F) mutation for the diagnosis of Ph- MPD was underscored, including entities with a low allele burden and the discrimination from reactive disorders (autoimmune myelofibrosis, reactive thrombocytosis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_provenance.
- NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_assertion evidence source_evidence_literature NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_provenance.
- NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_assertion SIO_000772 19605821 NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_provenance.
- NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_assertion wasDerivedFrom befree-20150227 NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_provenance.
- NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_assertion wasGeneratedBy ECO_0000203 NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP519091.RAPYsP-d7f6YfwH_yGctWTnh0lDmAZfcHcxZTHIHZv3-A130_provenance.