Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_provenance.
- NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_assertion description "[The most common cause of fragile X syndrome is expansion of a CGG trinucleotide repeat in the 5'UTR of FMR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_provenance.
- NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_assertion evidence source_evidence_literature NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_provenance.
- NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_assertion SIO_000772 18412117 NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_provenance.
- NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_assertion wasDerivedFrom befree-20150227 NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_provenance.
- NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_assertion wasGeneratedBy ECO_0000203 NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP431880.RAdBb_4QW7Nzv42QrNCsa9KhaQxhLN42DUMii4-uW-GSk130_provenance.