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- source_evidence_literature type ECO_0000212 NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_provenance.
- NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_assertion description "[The most common combination of gene mutations was APC and K-ras mutations (21.9%), followed by K-ras and p53 mutations (12.5%) and then APC and p53 mutations (10.4%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_provenance.
- NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_assertion evidence source_evidence_literature NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_provenance.
- NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_assertion SIO_000772 18265644 NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_provenance.
- NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_assertion wasDerivedFrom befree-2016 NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_provenance.
- NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_assertion wasGeneratedBy ECO_0000203 NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_provenance.
- befree-2016 importedOn "2016-02-19" NP654810.RAKn_LRFNZ8997xgF-iSl4RmK5GB52yEBu66_tdR1Ybxg130_provenance.