Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_provenance.
- NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_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." NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_provenance.
- NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_assertion evidence source_evidence_literature NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_provenance.
- NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_assertion SIO_000772 12745272 NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_provenance.
- NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_assertion wasDerivedFrom befree-2016 NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_provenance.
- NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_assertion wasGeneratedBy ECO_0000203 NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_provenance.
- befree-2016 importedOn "2016-02-19" NP394122.RANjrGV27GYE25jahJ8XvC9MlZrxwnAI37DZBNs7pLugo130_provenance.