Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_provenance.
- NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_assertion description "[Genetic testing of the 2 sisters and their mother (who also had multiple facial lentigines but did not have Cushing syndrome) revealed a novel mutation in the PRKAR1A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_provenance.
- NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_assertion evidence source_evidence_literature NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_provenance.
- NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_assertion SIO_000772 19833579 NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_provenance.
- NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_assertion wasDerivedFrom befree-2016 NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_provenance.
- NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_assertion wasGeneratedBy ECO_0000203 NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_provenance.
- befree-2016 importedOn "2016-02-19" NP769566.RAmQjWmbbq7_dcD6UtWGiR9m8YRX1dG-TP0cWmvNMkd88130_provenance.