Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance.
- NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_assertion description "[Point mutations in SPG4, the gene encoding spastin, are a frequent cause of autosomal dominant hereditary spastic paraplegia (AD-HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance.
- NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_assertion evidence source_evidence_literature NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance.
- NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_assertion SIO_000772 17098887 NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance.
- NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_assertion wasDerivedFrom befree-20140225 NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance.
- NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_assertion wasGeneratedBy ECO_0000203 NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance.