Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_provenance.
- NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_assertion description "[The aims of the present study are to discuss the clinical and molecular findings of two Brazilian patients with ACTH-independent CS due to PPNAD and to show the diagnostic challenge CS represents in childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_provenance.
- NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_assertion evidence source_evidence_literature NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_provenance.
- NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_assertion SIO_000772 20924687 NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_provenance.
- NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_assertion wasDerivedFrom befree-20140225 NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_provenance.
- NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_assertion wasGeneratedBy ECO_0000203 NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP626563.RAdw4WxKLRPNv6kxuQV2rgpLOiXMdHKjBncangU9c4ZyQ130_provenance.