Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP524537.RAWM6XW_l22ZsBjoDea-8Pdf6rjjzKWRONkAjUawKKEhU130_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." NP524537.RAWM6XW_l22ZsBjoDea-8Pdf6rjjzKWRONkAjUawKKEhU130_provenance.
- NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_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." NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_provenance.
- NP391521.RA3fJ5vkmbhgazR-QQ4y1JXq22wkC1uNeKzx2290xTVPA130_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." NP391521.RA3fJ5vkmbhgazR-QQ4y1JXq22wkC1uNeKzx2290xTVPA130_provenance.
- NP160092.RAyaVTlDhfKocUjvmuUdIUkMqlfIm2ziQqiGRszM4W5Ek130_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." NP160092.RAyaVTlDhfKocUjvmuUdIUkMqlfIm2ziQqiGRszM4W5Ek130_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.
- NP845249.RAKobEPz1HiZv-012lxswu9lgHLgRQ7PokF_vtd5if1Aw130_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." NP845249.RAKobEPz1HiZv-012lxswu9lgHLgRQ7PokF_vtd5if1Aw130_provenance.
- 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." provenance.
- NP831223.RAhsW9CJbGGm2siXv0WcoEDtUYbBJyzOXvQDvsAmPcpWs130_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." NP831223.RAhsW9CJbGGm2siXv0WcoEDtUYbBJyzOXvQDvsAmPcpWs130_provenance.
- NP1109883.RAFzCVvzDpp5uZ3y9TCDLLbv-FyfI9tI-UD0BUKXwmAx4130_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." NP1109883.RAFzCVvzDpp5uZ3y9TCDLLbv-FyfI9tI-UD0BUKXwmAx4130_provenance.