Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion> ?p ?o ?g. }
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- NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion type Assertion NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_head.
- NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion wasGeneratedBy ECO_0000203 NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.
- NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion wasDerivedFrom befree-2016 NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.
- NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion SIO_000772 15596607 NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.
- NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion evidence source_evidence_literature NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.
- NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion description "[This study enables us to estimate the frequency of the SPG3A mutations in France at 39% in families with young-onset autosomal dominant spastic paraplegia after exclusion of SPG4 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.