Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_assertion> ?p ?o ?g. }
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- NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_assertion type Assertion NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_head.
- NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_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." NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_provenance.
- NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_assertion evidence source_evidence_literature NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_provenance.
- NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_assertion SIO_000772 17646629 NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_provenance.
- NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_assertion wasDerivedFrom befree-20150227 NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_provenance.
- NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_assertion wasGeneratedBy ECO_0000203 NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_provenance.