Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_provenance.
- NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_assertion description "[Fragile X-associated tremor/ataxia syndrome is a late adult onset neurodegenerative disorder that affects individuals who carry a premutation CGG repeat expansion (55-200 CGG repeats) in the 5' untranslated portion of the fragile X mental retardation 1 (FMR1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_provenance.
- NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_assertion evidence source_evidence_literature NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_provenance.
- NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_assertion SIO_000772 19794313 NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_provenance.
- NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_assertion wasDerivedFrom befree-2016 NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_provenance.
- NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_assertion wasGeneratedBy ECO_0000203 NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_provenance.
- befree-2016 importedOn "2016-02-19" NP766574.RAEyyAlhacczS7Z5At2eBYGSarFPdxeRLvseAvUbzhJbo130_provenance.