Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_assertion type Assertion NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_head.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_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." NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_assertion evidence source_evidence_literature NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_assertion SIO_000772 18445050 NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_assertion wasDerivedFrom befree-20140225 NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_assertion wasGeneratedBy ECO_0000203 NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.