Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_provenance.
- NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_assertion wasGeneratedBy ECO_0000203 NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_provenance.
- NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_assertion wasDerivedFrom befree-2016 NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_provenance.
- NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_assertion SIO_000772 23790110 NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_provenance.
- NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_assertion evidence source_evidence_literature NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_provenance.
- NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_assertion description "[Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder associated with FMR1 gene premutation alleles (55-200 CGG repeats).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1087841.RAVw4_JclQE8_r8frWiGv3uW_vlgZeJ1p2KyMX2EAEX4U130_provenance.