Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_assertion type Assertion NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_head.
- NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_assertion description "[Mowat-Wilson syndrome (MWS) is an autosomal dominant developmental disorder with mental retardation and variable multiple congenital abnormalities due to mutations of the ZEB2 (ZFHX1B) gene at 2q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_provenance.
- NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_assertion evidence source_evidence_literature NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_provenance.
- NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_assertion SIO_000772 18445050 NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_provenance.
- NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_assertion wasDerivedFrom befree-20140225 NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_provenance.
- NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_assertion wasGeneratedBy ECO_0000203 NP662778.RAMucdiJFG5tKKuuUAtdm-8gwWsj8Sy2gJntifggtU6tM130_provenance.