Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_assertion> ?p ?o ?g. }
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- NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_assertion type Assertion NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_head.
- NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_assertion description "[This study was designed to detect wether the TNF2 allele is associated with disease progression in MS. We examined the TNFalpha -308 polymorphism with an allelic discrimination PCR to detect the G-->A transition in the genomic DNA of 283 MS patients from Germany and in 72 patients with amyotrophic lateral sclerosis (ALS) and 66 with stroke from the same genetic background who served as controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_provenance.
- NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_assertion evidence source_evidence_literature NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_provenance.
- NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_assertion SIO_000772 10552245 NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_provenance.
- NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_assertion wasDerivedFrom befree-2016 NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_provenance.
- NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_assertion wasGeneratedBy ECO_0000203 NP267134.RAKrp9kjfQHHW6Fw8j82wDrTzU-BnqAyH04LzoTHVS9DE130_provenance.