Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_provenance.
- NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_assertion description "[We demonstrate that the mutation S100P is associated with proteasome-mediated degradation, and thus presumably represents a null mutation comparable to the Ca8 mutation underlying the previously described waddles mouse, which exhibits ataxia and appendicular dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_provenance.
- NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_assertion evidence source_evidence_literature NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_provenance.
- NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_assertion SIO_000772 19461874 NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_provenance.
- NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_assertion wasDerivedFrom befree-20140225 NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_provenance.
- NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_assertion wasGeneratedBy ECO_0000203 NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP801320.RAbedz9xFPE4zxk2wki1sdeVTejsHZsmHRZ9iauWmMhxQ130_provenance.