Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_provenance.
- NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_assertion description "[In addition to mutations in genes known to be involved in leukemogenesis (ETV6, NOTCH1, JAK1, and NF1), we identified novel recurrent mutations in FAT1 (25%), FAT3 (20%), DNM2 (35%), and genes associated with epigenetic regulation (MLL2, BMI1, and DNMT3A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_provenance.
- NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_assertion evidence source_evidence_literature NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_provenance.
- NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_assertion SIO_000772 23603912 NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_provenance.
- NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_assertion wasDerivedFrom befree-2016 NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_provenance.
- NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_assertion wasGeneratedBy ECO_0000203 NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1071149.RAh8igxtTfzGw6jhzI4nR57hplDDR7Y6hIEIZvvt1WwZg130_provenance.