Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_provenance.
- NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_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." NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_provenance.
- NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_assertion evidence source_evidence_curated NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_provenance.
- NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_assertion SIO_000772 8882880 NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_provenance.
- NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_assertion wasDerivedFrom uniprot-2016 NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_provenance.
- NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_assertion wasGeneratedBy ECO_0000218 NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9193.RA8bsnt0Std_22pQaQcET6tSD06MgBuK415NDgmKv-bo4130_provenance.