Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_assertion> ?p ?o ?g. }
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- NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_assertion type Assertion NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_head.
- 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.
- NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_assertion evidence source_evidence_literature NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_provenance.
- NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_assertion SIO_000772 18445050 NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_provenance.
- NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_assertion wasDerivedFrom befree-20140225 NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_provenance.
- NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_assertion wasGeneratedBy ECO_0000203 NP538413.RAhmUnwaBy9yvxGrbTPkAjR_6irFzVt_LAW1fTb6oZBOI130_provenance.