Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_assertion> ?p ?o ?g. }
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- NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_assertion type Assertion NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_head.
- NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_assertion wasGeneratedBy ECO_0000203 NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_provenance.
- NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_assertion wasDerivedFrom befree-2016 NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_provenance.
- NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_assertion SIO_000772 21545237 NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_provenance.
- NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_assertion evidence source_evidence_literature NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_provenance.
- NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_assertion description "[Sporadic motor neuron disease in a familial novel SOD1 mutation: incomplete penetrance or chance association?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP891956.RAs0RKGoDV05TQd87EkQY7ncrEQN_YWkIYZfyBtZdPI_k130_provenance.