Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion> ?p ?o ?g. }
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- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion type Assertion NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_head.
- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_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." NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion evidence source_evidence_literature NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion SIO_000772 17646629 NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion wasDerivedFrom lhgdn-20090331 NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion wasGeneratedBy ECO_0000203 NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.