Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_provenance.
- NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_assertion wasGeneratedBy ECO_0000203 NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_provenance.
- NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_assertion wasDerivedFrom befree-20140225 NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_provenance.
- NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_assertion SIO_000772 22167411 NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_provenance.
- NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_assertion evidence source_evidence_literature NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_provenance.
- NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_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." NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP237680.RAsqhrA873IEPxxIr3bzOttQX-DtIBBJTc1u4oZj_dTJc130_provenance.