Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the 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.
- NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion evidence source_evidence_literature NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.
- NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion SIO_000772 15596607 NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.
- NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion wasDerivedFrom befree-2016 NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.
- NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_assertion wasGeneratedBy ECO_0000203 NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.
- befree-2016 importedOn "2016-02-19" NP472581.RABCciGGPss3d6x1NuCTyR8xfU80UpWFWeDLyRDqJUPus130_provenance.