Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_provenance.
- NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_assertion description "[Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_provenance.
- NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_assertion evidence source_evidence_literature NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_provenance.
- NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_assertion SIO_000772 23889083 NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_provenance.
- NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_assertion wasDerivedFrom befree-20150227 NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_provenance.
- NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_assertion wasGeneratedBy ECO_0000203 NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP881225.RAtNeGThOtozxSKVXjkLJzRyMsiyj7YSjchb7qinSeYE8130_provenance.