Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_provenance.
- NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_assertion description "[For four mutations affecting ATRX (p.1761M>T), PQBP1 (p.155R>X) and SLC6A8 (p.390P>L and p.477S>L), we provide evidence for a functional involvement of these changes in the aetiology of intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_provenance.
- NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_assertion evidence source_evidence_literature NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_provenance.
- NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_assertion SIO_000772 21267006 NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_provenance.
- NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_assertion wasDerivedFrom befree-2016 NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_provenance.
- NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_assertion wasGeneratedBy ECO_0000203 NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_provenance.
- befree-2016 importedOn "2016-02-19" NP867769.RA_XXjDNP0IzO9Nvdy1WklHkM41H1K-0kMSxoF13VP6Y0130_provenance.