Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_provenance.
- NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_assertion description "[Primary Pigmented Nodular Adrenocortical Disease (PPNAD) is a rare form of bilateral adrenocortical hyperplasia that is inherited in an autosomal dominant manner and leads to ACTH-independent Cushing's syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_provenance.
- NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_assertion evidence source_evidence_literature NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_provenance.
- NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_assertion SIO_000772 20924687 NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_provenance.
- NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_assertion wasDerivedFrom befree-20150227 NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_provenance.
- NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_assertion wasGeneratedBy ECO_0000203 NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP634338.RApc0ET3_XSAmrtylDTa6YHY3eOMra-q5ch7EZpCU4EYs130_provenance.