Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_provenance.
- NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_assertion description "[Instead, we identified deletion of the p16 (CDKN2A) and retinoblastoma (RB1) genes as likely causal events leading to increased AURKA and CINSARC gene expression, to chromosome rearrangement, and ultimately to metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_provenance.
- NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_assertion evidence source_evidence_literature NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_provenance.
- NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_assertion SIO_000772 22167411 NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_provenance.
- NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_assertion wasDerivedFrom befree-2016 NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_provenance.
- NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_assertion wasGeneratedBy ECO_0000203 NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_provenance.
- befree-2016 importedOn "2016-02-19" NP946476.RASvt568moogtO-6ce0pgW_pzFRVGObhYB0RS1eJdsaxU130_provenance.