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- source_evidence_literature type ECO_0000212 NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_provenance.
- NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_assertion description "[Werner syndrome (WS) is a rare autosomal progeroid disorder caused by a mutation in the gene encoding the WRN (Werner syndrome protein), a member of the RecQ family of helicases with a role in maintaining genomic stability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_provenance.
- NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_assertion evidence source_evidence_literature NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_provenance.
- NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_assertion SIO_000772 19064679 NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_provenance.
- NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_assertion wasDerivedFrom befree-2016 NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_provenance.
- NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_assertion wasGeneratedBy ECO_0000203 NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP707853.RAT3ybNXc57GmUwXxtoO-BP3ukGsTW3WB-BdOSS0wa2qQ130_provenance.