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- source_evidence_literature type ECO_0000212 NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_provenance.
- NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_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." NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_provenance.
- NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_assertion evidence source_evidence_literature NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_provenance.
- NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_assertion SIO_000772 17133502 NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_provenance.
- NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_assertion wasDerivedFrom befree-20150227 NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_provenance.
- NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_assertion wasGeneratedBy ECO_0000203 NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP408699.RAxQrg2D-nHYOSZp2yyl3j-3vRkgV7gFA1fPI6rw59ETI130_provenance.