Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_provenance.
- NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_assertion description "[This hypothesis is supported by the finding of decreased adenosine deaminase (ADA) activity in the sera of some children with autism and reports of an association of the A allele of the ADA G22A (Asp8Asn) polymorphism in individuals with autism of Italian-descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_provenance.
- NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_assertion evidence source_evidence_literature NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_provenance.
- NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_assertion SIO_000772 17340203 NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_provenance.
- NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_assertion wasDerivedFrom befree-20140225 NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_provenance.
- NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_assertion wasGeneratedBy ECO_0000203 NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401003.RA0s7fOkFwQvqgd042nIUtBYH68R6tfJqIdaaXgbVbVyE130_provenance.