Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_provenance.
- NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_assertion description "[In total, 35 of 43 (81%) subjects with Ollier disease and 10 of 13 (77%) with Maffucci syndrome carried IDH1 (98%) or IDH2 (2%) mutations in their tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_provenance.
- NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_assertion evidence source_evidence_literature NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_provenance.
- NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_assertion SIO_000772 22057234 NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_provenance.
- NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_assertion wasDerivedFrom befree-20140225 NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_provenance.
- NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_assertion wasGeneratedBy ECO_0000203 NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP241833.RAVm_bByRbrAFwMcGV9CkX3FEQZTKFBB_XrkRJ8tKI_hM130_provenance.