Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_assertion> ?p ?o ?g. }
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- NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_assertion type Assertion NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_head.
- NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_assertion description "[First, we established HeLa cell lines stably expressing DHODH with Miller syndrome-causative mutations: G202A, R346W and R135C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_provenance.
- NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_assertion evidence source_evidence_literature NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_provenance.
- NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_assertion SIO_000772 22967083 NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_provenance.
- NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_assertion wasDerivedFrom befree-20140225 NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_provenance.
- NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_assertion wasGeneratedBy ECO_0000203 NP404761.RAyk9ZYDVz8sDG5sAOisTf4V8K4YW_Te2rmjyeO8xbZNo130_provenance.