Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_provenance.
- NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_assertion wasGeneratedBy ECO_0000203 NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_provenance.
- NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_assertion wasDerivedFrom befree-20140225 NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_provenance.
- NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_assertion SIO_000772 15741255 NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_provenance.
- NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_assertion evidence source_evidence_literature NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_provenance.
- NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_assertion description "[In a patient with HLRCC caused by a germline-inactivating FH mutation, we diagnosed atypical (subclinical) CS due to bilateral, ACTH-independent adrenocortical hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP383914.RAAlhQ9Uezxia14XEaEoUv0HePsC8Si__1w7kBTSPmtPE130_provenance.