Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_provenance.
- befree-20150227 importedOn "2015-02-27" NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_provenance.
- NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_assertion wasGeneratedBy ECO_0000203 NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_provenance.
- NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_assertion wasDerivedFrom befree-20150227 NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_provenance.
- NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_assertion SIO_000772 22167411 NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_provenance.
- NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_assertion evidence source_evidence_literature NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_provenance.
- NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_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." NP306931.RACeH5EiITvzpQQN1U7ChYZ9507rk__MJCn5v2MrwSQng130_provenance.