Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_assertion> ?p ?o ?g. }
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- NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_assertion type Assertion NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_head.
- NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_assertion description "[The X-linked lethal Ogden syndrome was the first reported human genetic disorder associated with a mutation in an N-terminal acetyltransferase (NAT) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_provenance.
- NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_assertion evidence source_evidence_literature NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_provenance.
- NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_assertion SIO_000772 25489052 NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_provenance.
- NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_assertion wasDerivedFrom befree-2016 NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_provenance.
- NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_assertion wasGeneratedBy ECO_0000203 NP1246338.RAo93a3Mp-PvBgSw3U6py6zlL7e7LFL5Z9k6dnGAd39oM130_provenance.