Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_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." NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_provenance.
• NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_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." NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_provenance.
• 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.
• 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.
• NP760759.RA0ATAHe89Fb8Lv79qhKN1VT58xKKAXKbl7QXalfCd6NE130_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." NP760759.RA0ATAHe89Fb8Lv79qhKN1VT58xKKAXKbl7QXalfCd6NE130_provenance.
• 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.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_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." NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_provenance.
• NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_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." NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_provenance.
• NP668462.RAuW2E3mWDJcMe_29deptJNucDxZ3EVs6CS_dwGcSjLEQ130_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." NP668462.RAuW2E3mWDJcMe_29deptJNucDxZ3EVs6CS_dwGcSjLEQ130_provenance.
• NP831050.RAyfpZVA8M5RPZKXX86TXxAqorhf_H7LFHhPoWAybP860130_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." NP831050.RAyfpZVA8M5RPZKXX86TXxAqorhf_H7LFHhPoWAybP860130_provenance.
• NP668463.RA9im7e7EJnVI9nKninKNcrEGMAvrYsghriIRpwdT8NIY130_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." NP668463.RA9im7e7EJnVI9nKninKNcrEGMAvrYsghriIRpwdT8NIY130_provenance.