Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_provenance.
- NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_assertion description "[Premutation alleles of the fragile X mental retardation 1 (FMR1) gene give rise to a late-onset movement disorder, fragile X-associated tremor/ataxia syndrome (FXTAS), characterized by progressive intention tremor and gait ataxia, with associated dementia and global brain atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_provenance.
- NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_assertion evidence source_evidence_literature NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_provenance.
- NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_assertion SIO_000772 17133502 NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_provenance.
- NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_assertion wasDerivedFrom befree-20140225 NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_provenance.
- NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_assertion wasGeneratedBy ECO_0000203 NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP193113.RApuIFLtgfVHRw4w3gDvxeiWSQu160RLnbg9yog_C0G6c130_provenance.