Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_assertion> ?p ?o ?g. }
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- NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_assertion type Assertion NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_head.
- NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_assertion wasGeneratedBy ECO_0000203 NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_provenance.
- NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_assertion wasDerivedFrom gad-20130706 NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_provenance.
- NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_assertion SIO_000772 18162506 NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_provenance.
- NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_assertion evidence source_evidence_literature NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_provenance.
- NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_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." NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_provenance.