Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_provenance.
- NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_assertion description "[We have reported previously nonsense inactivating mutations of the phosphodiesterase 11A (PDE11A) gene in patients with micronodular adrenocortical hyperplasia and Cushing syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_provenance.
- NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_assertion evidence source_evidence_literature NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_provenance.
- NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_assertion SIO_000772 18559625 NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_provenance.
- NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_assertion wasDerivedFrom befree-20140225 NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_provenance.
- NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_assertion wasGeneratedBy ECO_0000203 NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP680561.RA0FOB0otgIrALm4sswC2laRkDBgzvK3bAd95sMc1rMhI130_provenance.