Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance.
- 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.
- gad-20130706 importedOn "2013-07-06" NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance.