Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_assertion> ?p ?o ?g. }
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- NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_assertion type Assertion NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_head.
- NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_provenance.
- NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_assertion evidence source_evidence_literature NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_provenance.
- NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_assertion SIO_000772 20857310 NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_provenance.
- NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_assertion wasDerivedFrom befree-20140225 NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_provenance.
- NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_assertion wasGeneratedBy ECO_0000203 NP713922.RAUUVWtEMqAoIewYPRtZIUx-u2GVMOeBjqeneKcatiTUA130_provenance.