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- NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_assertion type Assertion NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_head.
- NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_provenance.
- NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_assertion evidence source_evidence_literature NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_provenance.
- NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_assertion SIO_000772 17646629 NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_provenance.
- NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_assertion wasDerivedFrom lhgdn-20090331 NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_provenance.
- NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_assertion wasGeneratedBy ECO_0000203 NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_provenance.