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- source_evidence_literature type ECO_0000212 NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_provenance.
- NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_assertion description "[Mutations in AQP2 cause autosomal nephrogenic diabetes insipidus (NDI), a disease that renders the kidney unresponsive to vasopressin, resulting in polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_provenance.
- NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_assertion evidence source_evidence_literature NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_provenance.
- NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_assertion SIO_000772 19701945 NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_provenance.
- NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_assertion wasDerivedFrom befree-2016 NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_provenance.
- NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_assertion wasGeneratedBy ECO_0000203 NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_provenance.
- befree-2016 importedOn "2016-02-19" NP759128.RA01okGS09Id9iUYvhX3m9YVLyNpovobFP_0D4h3W0tfU130_provenance.