Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_provenance.
- NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_assertion description "[Significant differences in OS were observed for SM mutated patients grouped based on the presence of combined TET2/DNMT3A/ASXL1 mutations independent of KIT (P = 0.04) and sole TET2 mutations (P<0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_provenance.
- NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_assertion evidence source_evidence_literature NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_provenance.
- NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_assertion SIO_000772 22905207 NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_provenance.
- NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_assertion wasDerivedFrom befree-2016 NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_provenance.
- NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_assertion wasGeneratedBy ECO_0000203 NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1006496.RApIYBsErTBK-EwLs6SkHsWDcVecL751ipO4--vAqFYtw130_provenance.