Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_provenance.
- NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_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." NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_provenance.
- NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_assertion evidence source_evidence_literature NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_provenance.
- NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_assertion SIO_000772 18559625 NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_provenance.
- NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_assertion wasDerivedFrom befree-2016 NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_provenance.
- NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_assertion wasGeneratedBy ECO_0000203 NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_provenance.
- befree-2016 importedOn "2016-02-19" NP677137.RAOo-U8chHXCJEJRYy3A8yYqkcrYrtzOa4PS9CpfRqRGg130_provenance.