Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_provenance.
- NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_assertion description "[Expansion of GAA repeats in the intron of this gene is involved in the autosomal recessive Friedreich ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_provenance.
- NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_assertion evidence source_evidence_literature NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_provenance.
- NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_assertion SIO_000772 12354077 NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_provenance.
- NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_assertion wasDerivedFrom lhgdn-20090331 NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_provenance.
- NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_assertion wasGeneratedBy ECO_0000203 NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP199109.RAJ-4716TqGd8DpekLIErK_Nw98Hj83jIC-8Gm74Xbs-k130_provenance.