Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_provenance.
- NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_assertion description "[Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_provenance.
- NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_assertion evidence source_evidence_literature NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_provenance.
- NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_assertion SIO_000772 7719135 NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_provenance.
- NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_assertion wasDerivedFrom befree-20150227 NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_provenance.
- NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_assertion wasGeneratedBy ECO_0000203 NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP900916.RAnfh4RAg2VvJYCUoH3LrMBPe8TNzNLklolWevje9epbk130_provenance.