Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_provenance.
- NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_assertion description "[Importantly, we verified the high rate of DNMT3A mutations (16%) in a larger cohort of adult patients with ETP-ALL (10/68).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_provenance.
- NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_assertion evidence source_evidence_literature NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_provenance.
- NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_assertion SIO_000772 23603912 NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_provenance.
- NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_assertion wasDerivedFrom befree-20140225 NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_provenance.
- NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_assertion wasGeneratedBy ECO_0000203 NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP926530.RAiFueQu0P7zWZ81koBJzJgNjxf0FZREKmrI5AGJXXN-o130_provenance.