Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion> ?p ?o ?g. }
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- NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion type Assertion NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_head.
- NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion description "[These results suggest that the frequency of SPAST mutations is higher among Japanese patients with autosomal dominant Hereditary spastic paraplegia (HSP), although SPAST mutations are also observed in patients with sporadic spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_provenance.
- NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion evidence source_evidence_literature NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_provenance.
- NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion SIO_000772 16788734 NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_provenance.
- NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion wasDerivedFrom lhgdn-20090331 NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_provenance.
- NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion wasGeneratedBy ECO_0000203 NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_provenance.