Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_provenance.
- NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_assertion description "[Mutations in the vasopressin V2 receptor and aquaporin-2 genes in 12 families with congenital nephrogenic diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_provenance.
- NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_assertion evidence source_evidence_curated NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_provenance.
- NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_assertion SIO_000772 9402087 NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_provenance.
- NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_assertion wasDerivedFrom uniprot-20130724 NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_provenance.
- NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_assertion wasGeneratedBy ECO_0000218 NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP461.RALdeW8YkuVA98dDHHz1BQNMLqhcrA7r41I6XNm4ujev4130_provenance.