Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_provenance.
- NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_assertion description "[Expansion of a (CGG)n trinucleotide repeat unit at FRAXE, a newly defined fragile site distal to FRAXA, at Xq28, is reported to be associated with mild mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_provenance.
- NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_assertion evidence source_evidence_literature NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_provenance.
- NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_assertion SIO_000772 7541938 NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_provenance.
- NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_assertion wasDerivedFrom befree-20140225 NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_provenance.
- NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_assertion wasGeneratedBy ECO_0000203 NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP572100.RAWLZj0OJKQ6JbhZNLuB2bIesb68ushlL1ABFB4odNuNA130_provenance.