Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_assertion> ?p ?o ?g. }
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- NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_assertion type Assertion NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_head.
- NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_assertion description "[The frequency for SPG4 mutations detected in autosomal dominant hereditary spastic paraplegia was 44.4%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_provenance.
- NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_assertion evidence source_evidence_literature NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_provenance.
- NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_assertion SIO_000772 16684598 NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_provenance.
- NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_assertion wasDerivedFrom befree-20150227 NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_provenance.
- NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_assertion wasGeneratedBy ECO_0000203 NP710047.RAJHO-lL95WDX3QAg_aq1uxzx40uacmCuMlW7ALCLFTMs130_provenance.