Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_provenance.
- befree-2016 importedOn "2016-02-19" NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_provenance.
- NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_assertion wasGeneratedBy ECO_0000203 NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_provenance.
- NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_assertion wasDerivedFrom befree-2016 NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_provenance.
- NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_assertion SIO_000772 16060937 NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_provenance.
- NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_assertion evidence source_evidence_literature NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_provenance.
- NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_assertion description "[Choreoacanthocytosis (ChAc) is an autosomal recessive disorder caused by mutations in VPS13A on chromosome 9q21 and characterized by neurodegeneration and red cell acanthocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506700.RASiQVogc8Q5jSH9dtZPSU5Cl7qigmww_f7jaXxXAEWqY130_provenance.