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- source_evidence_literature type ECO_0000212 NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_provenance.
- NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_assertion wasGeneratedBy ECO_0000203 NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_provenance.
- NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_assertion wasDerivedFrom befree-20150227 NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_provenance.
- NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_assertion SIO_000772 24451280 NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_provenance.
- NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_assertion evidence source_evidence_literature NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_provenance.
- NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_assertion description "[Sequencing analysis revealed that UCs harbored somatic mutations in PIK3CA (50%), CTNNB1 (30%), TP53 (30%), FBXW7 (20%), and PPP2R1A (20%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751807.RAS9TkFjV4I-9UD9sMAk3bhXS9lLd_87j7M-EElQw3rYg130_provenance.