Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_provenance.
- NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_assertion description "[We identify three new CIN-suppressor genes (PIGN (also known as MCD4), MEX3C (RKHD2) and ZNF516 (KIAA0222)) encoded on chromosome 18q that are subject to frequent copy number loss in CIN(+) CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_provenance.
- NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_assertion evidence source_evidence_literature NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_provenance.
- NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_assertion SIO_000772 23446422 NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_provenance.
- NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_assertion wasDerivedFrom befree-2016 NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_provenance.
- NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_assertion wasGeneratedBy ECO_0000203 NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1056468.RAOgErexcu7nM25mfVG13pesKCUosKUgtz9CS6Wz2TgOA130_provenance.