Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_provenance.
- NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_assertion description "[We, therefore, investigated individuals from families with one or more first-degree relatives with myelodysplastic syndrome/acute myeloid leukemia with wild-type RUNX1 and CEBPA, for GATA2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_provenance.
- NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_assertion evidence source_evidence_literature NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_provenance.
- NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_assertion SIO_000772 22271902 NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_provenance.
- NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_assertion wasDerivedFrom befree-20140225 NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_provenance.
- NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_assertion wasGeneratedBy ECO_0000203 NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP586178.RAnUkmX9NwCKni4N_RDKFfWZi19sqC_dsxTfeszyvZiJQ130_provenance.