Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_assertion> ?p ?o ?g. }
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- NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_assertion type Assertion NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_head.
- NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_assertion wasGeneratedBy ECO_0000203 NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_provenance.
- NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_assertion wasDerivedFrom befree-20140225 NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_provenance.
- NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_assertion SIO_000772 24029077 NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_provenance.
- NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_assertion evidence source_evidence_literature NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_provenance.
- NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_assertion description "[Individuals with Mowat-Wilson syndrome (MWS; OMIM#235730) have characteristic facial features, a variety of congenital anomalies such as Hirschsprung disease, and intellectual disabilities caused by mutation or deletion of ZEB2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713194.RAPxVHhNeE7C3JTVZt-x_I_Dq69hRmzURLbkkmTwDdaIQ130_provenance.