Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_provenance.
- NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_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." NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_provenance.
- NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_assertion evidence source_evidence_literature NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_provenance.
- NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_assertion SIO_000772 17133502 NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_provenance.
- NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_assertion wasDerivedFrom befree-2016 NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_provenance.
- NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_assertion wasGeneratedBy ECO_0000203 NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_provenance.
- befree-2016 importedOn "2016-02-19" NP581611.RAS16Un74i_ODTNRR2XlvM5GqI0sDx5ZQD9iTfuo2KgcU130_provenance.