Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_provenance.
- NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_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." NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_provenance.
- NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_assertion evidence source_evidence_literature NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_provenance.
- NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_assertion SIO_000772 19701945 NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_provenance.
- NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_assertion wasDerivedFrom befree-2016 NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_provenance.
- NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_assertion wasGeneratedBy ECO_0000203 NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_provenance.
- befree-2016 importedOn "2016-02-19" NP759129.RA54Fx2Z1Xvu5vKEaBnYvdvcrGIxPCgdTzApQywY7F5Eo130_provenance.