Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_assertion> ?p ?o ?g. }
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- NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_assertion type Assertion NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_head.
- NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_assertion wasGeneratedBy ECO_0000203 NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance.
- NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_assertion wasDerivedFrom gad-20130706 NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance.
- NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_assertion SIO_000772 18162506 NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance.
- NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_assertion evidence source_evidence_literature NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance.
- NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_assertion description "[INS mutations are the second most common cause of PND and a rare cause of MODY.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance.