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- source_evidence_literature type ECO_0000212 NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_provenance.
- NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_assertion description "[Nine patients (25.7%) with SCC and 6 patients (23.1%) with Ad were shown to have mutations of the p53 gene by single-strand conformation polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_provenance.
- NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_assertion evidence source_evidence_literature NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_provenance.
- NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_assertion SIO_000772 10023701 NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_provenance.
- NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_assertion wasDerivedFrom befree-2016 NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_provenance.
- NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_assertion wasGeneratedBy ECO_0000203 NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_provenance.
- befree-2016 importedOn "2016-02-19" NP245828.RA_J_Zd4_7fhKdN2zrrnOkuENMIYHQ17HGucFhbPUoxmg130_provenance.