Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_provenance.
- NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_assertion description "[MDM2 amplification in the face of chromosome 12 diploidy was seen in 8%, while another 8% had trisomy 12 with an equivalent increase in signals for MDM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_provenance.
- NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_assertion evidence source_evidence_literature NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_provenance.
- NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_assertion SIO_000772 12745272 NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_provenance.
- NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_assertion wasDerivedFrom befree-20140225 NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_provenance.
- NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_assertion wasGeneratedBy ECO_0000203 NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP250101.RAd9iCkoD51iQG_O1k6n9-G2tmC5iXBxG7appG2ByBsMI130_provenance.