Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_provenance.
- NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_assertion description "[Two novel mutations in the aquaporin-2 and the vasopressin V2 receptor genes in patients with congenital nephrogenic diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_provenance.
- NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_assertion evidence source_evidence_literature NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_provenance.
- NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_assertion SIO_000772 8882880 NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_provenance.
- NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_assertion wasDerivedFrom befree-2016 NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_provenance.
- NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_assertion wasGeneratedBy ECO_0000203 NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1360888.RAUnnj9L4dmITQAYh7USqMe2KpQ0hD52G2WFbP7VXX9cA130_provenance.