Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_assertion type Assertion NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_head.
- NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_assertion wasGeneratedBy ECO_0000203 NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_provenance.
- NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_assertion wasDerivedFrom befree-2016 NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_provenance.
- NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_assertion SIO_000772 23771172 NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_provenance.
- NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_assertion evidence source_evidence_literature NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_provenance.
- NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_assertion description "[We selected 29 genes in which mutations have been reported to cause neonatal diabetes, MODY, maternally inherited diabetes and deafness (MIDD) or familial partial lipodystrophy (FPLD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1086325.RAmT08Mhfpx5CnzEgIlgyhw5_BLBqjHJrESWx5RYdtOA8130_provenance.