Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_assertion> ?p ?o ?g. }
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- NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_assertion type Assertion NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_head.
- NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_assertion description "[ To our knowledge, this is the first report of SPG4 mutations in the People's Republic of China. The percentage of involved Chinese families with autosomal dominant hereditary spastic paraplegia with an SPG4 mutation is 18% (4/22), lower than the estimated 40% linked to this locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_provenance.
- NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_assertion evidence source_evidence_literature NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_provenance.
- NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_assertion SIO_000772 14732620 NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_provenance.
- NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_assertion wasDerivedFrom gad-20130706 NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_provenance.
- NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_assertion wasGeneratedBy ECO_0000203 NP51143.RA7QvPchg3KMloRdrAbG8nDuMCbopofTCy7qfwNVkRN0Q130_provenance.