Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_provenance.
- befree-2016 importedOn "2016-02-19" NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_provenance.
- NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_assertion wasGeneratedBy ECO_0000203 NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_provenance.
- NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_assertion wasDerivedFrom befree-2016 NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_provenance.
- NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_assertion SIO_000772 12215255 NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_provenance.
- NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_assertion evidence source_evidence_literature NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_provenance.
- NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_assertion description "[Fragile X syndrome linked to the FRAXA locus is the most common inherited genetic disease accounting for mental retardation and is usually caused by the expansion of an unstable CGG repeat in the first exon of the FMR1 gene on the X chromosome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367102.RAEo_UVdy7XS1OrnOBr4uJrdxndFcfLqoYa63mMFsp_-s130_provenance.