Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_provenance.
- NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_assertion description "[It is not clear if or how MMR would affect instability of disease-causing expanded trinucleotide repeat sequences that adopt secondary structures other than hairpins, such as the triplex/R-loop forming (GAA�TTC)(n) sequence that causes Friedreich ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_provenance.
- NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_assertion evidence source_evidence_literature NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_provenance.
- NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_assertion SIO_000772 23071719 NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_provenance.
- NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_assertion wasDerivedFrom befree-20140225 NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_provenance.
- NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_assertion wasGeneratedBy ECO_0000203 NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP191378.RAHIWgeZHK041zc7yvoInfZuOuS8Iec6xhroJwch4sipM130_provenance.