Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_provenance.
- NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_assertion description "[The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_provenance.
- NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_assertion evidence source_evidence_literature NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_provenance.
- NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_assertion SIO_000772 18400758 NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_provenance.
- NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_assertion wasDerivedFrom befree-20150227 NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_provenance.
- NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_assertion wasGeneratedBy ECO_0000203 NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP469663.RAjjM5k2WP37_ysQZFQzTqkKPJygKQ1dOnnmB_GVhhhq4130_provenance.