Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_assertion> ?p ?o ?g. }
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- NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_assertion type Assertion NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_head.
- NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_assertion description "[The lamin A/C (LMNA) gene, mutations of which cause rare syndromes of severe insulin resistance and dyslipidemia, is located on chromosome 1q21-q24, a region linked to T2DM in several genome wide scans, including in the Old Order Amish.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_provenance.
- NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_assertion evidence source_evidence_literature NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_provenance.
- NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_assertion SIO_000772 15205219 NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_provenance.
- NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_assertion wasDerivedFrom befree-2016 NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_provenance.
- NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_assertion wasGeneratedBy ECO_0000203 NP448734.RAJr4-tXl8Aig7XYrIFjedrYNGPiXDGBgoHk7Ds0YugSw130_provenance.