Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion description "[Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion evidence source_evidence_literature NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion SIO_000772 20384727 NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion wasDerivedFrom befree-2016 NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion wasGeneratedBy ECO_0000203 NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- befree-2016 importedOn "2016-02-19" NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.