Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_provenance.
- NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_assertion description "[We studied 11 individuals with renal tubular dysgenesis, belonging to nine families, and found that they had homozygous or compound heterozygous mutations in the genes encoding renin, angiotensinogen, angiotensin converting enzyme or angiotensin II receptor type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_provenance.
- NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_assertion evidence source_evidence_curated NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_provenance.
- NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_assertion SIO_000772 16116425 NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_provenance.
- NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_assertion wasDerivedFrom ctd_human-20150221 NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_provenance.
- NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_assertion wasGeneratedBy ECO_0000218 NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP5543.RAcUVEFaixu32RYCfqCAEOEs0SYqPxHBIYu2iLPys7rWc130_provenance.