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- NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_assertion type Assertion NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_head.
- NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_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 (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_provenance.
- NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_assertion evidence source_evidence_literature NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_provenance.
- NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_assertion SIO_000772 17646629 NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_provenance.
- NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_assertion wasDerivedFrom befree-2016 NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_provenance.
- NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_assertion wasGeneratedBy ECO_0000203 NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_provenance.