Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_provenance.
- NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_assertion description "[Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive lipid storage disease caused by mutations in the cytochrome P450(27) (CYP27) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_provenance.
- NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_assertion evidence source_evidence_literature NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_provenance.
- NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_assertion SIO_000772 8728324 NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_provenance.
- NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_assertion wasDerivedFrom befree-20150227 NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_provenance.
- NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_assertion wasGeneratedBy ECO_0000203 NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP345664.RAvvzwhJItooH5EjenEfulwAseMc6lpGh9nwLXGou9ZA8130_provenance.