Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_assertion> ?p ?o ?g. }
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- NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_assertion type Assertion NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_head.
- NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_assertion wasGeneratedBy ECO_0000203 NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_provenance.
- NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_assertion wasDerivedFrom gad-20130706 NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_provenance.
- NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_assertion SIO_000772 18162506 NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_provenance.
- NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_assertion evidence source_evidence_literature NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_provenance.
- NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_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." NP86687.RAVYpTVNxWSegsw0po_IDOyE-JRHQj2qSB1IoYnMuFgKM130_provenance.