Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance.
- NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_assertion description "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance.
- NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_assertion evidence source_evidence_literature NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance.
- NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_assertion SIO_000772 9302264 NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance.
- NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_assertion wasDerivedFrom befree-20150227 NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance.
- NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_assertion wasGeneratedBy ECO_0000203 NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP258146.RA4qNwpIA1BXe-ZqvmkIxjWxqMt-aw588Jh3emZwx23Gg130_provenance.