Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_provenance.
- NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_assertion description "[The Fragile X-Related 1 gene (FXR1) is a paralog of the Fragile X Mental Retardation 1 gene (FMR1), whose absence causes the Fragile X syndrome, the most common form of inherited intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_provenance.
- NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_assertion evidence source_evidence_literature NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_provenance.
- NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_assertion SIO_000772 23555284 NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_provenance.
- NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_assertion wasDerivedFrom befree-20140225 NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_provenance.
- NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_assertion wasGeneratedBy ECO_0000203 NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP463865.RAi8cMBxncrn7Kr22Yw6QgUWmN0eKjpNtymp9y9mSJYZA130_provenance.