Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_provenance.
- NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_assertion description "[The syndrome of apparent mineralocorticoid excess (AME) is an inherited form of human hypertension thought to result from a deficiency of 11 beta-hydroxysteroid dehydrogenase (11 beta HSD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_provenance.
- NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_assertion evidence source_evidence_curated NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_provenance.
- NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_assertion SIO_000772 7670488 NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_provenance.
- NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_assertion wasDerivedFrom ctd_human-20150221 NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_provenance.
- NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_assertion wasGeneratedBy ECO_0000218 NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP17670.RAPmDu24hRUUB6Wp8ldWsRRD-WOxk_26FDWSYRY_aXxPc130_provenance.