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- source_evidence_literature type ECO_0000212 NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_provenance.
- NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_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." NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_provenance.
- NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_assertion evidence source_evidence_literature NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_provenance.
- NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_assertion SIO_000772 18559625 NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_provenance.
- NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_assertion wasDerivedFrom befree-20150227 NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_provenance.
- NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_assertion wasGeneratedBy ECO_0000203 NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP899097.RAOgyMvAL4z0ye79cT34tcvFyHReVfbakicydh7gX6WxA130_provenance.