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- source_evidence_literature type ECO_0000212 NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_provenance.
- NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_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." NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_provenance.
- NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_assertion evidence source_evidence_literature NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_provenance.
- NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_assertion SIO_000772 24451280 NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_provenance.
- NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_assertion wasDerivedFrom befree-20150227 NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_provenance.
- NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_assertion wasGeneratedBy ECO_0000203 NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP336377.RAticmuNjHPOELmgzS65Hos64JS1JwhG0ho9-Uqdw3W7I130_provenance.