Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance.
- NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance.
- NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_assertion evidence source_evidence_literature NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance.
- NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_assertion SIO_000772 21088058 NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance.
- NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_assertion wasDerivedFrom befree-2016 NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance.
- NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_assertion wasGeneratedBy ECO_0000203 NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance.
- befree-2016 importedOn "2016-02-19" NP853299.RAvHNihqA72Qb-P35Hgz4tRmb2K-8MOnXl1qp7H96dCFg130_provenance.