Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_assertion> ?p ?o ?g. }
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- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_assertion type Assertion NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_head.
- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_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." NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_assertion evidence source_evidence_literature NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_assertion SIO_000772 18445050 NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_assertion wasDerivedFrom befree-20140225 NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_assertion wasGeneratedBy ECO_0000203 NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.