Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_assertion type Assertion NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_head.
- 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.
- NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_assertion evidence source_evidence_literature NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_provenance.
- NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_assertion SIO_000772 24029077 NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_provenance.
- NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_assertion wasDerivedFrom befree-20140225 NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_provenance.
- NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_assertion wasGeneratedBy ECO_0000203 NP724100.RADDWgQKahb2bjIiIGUs0uKrGhR82jm5Or36Vb10wE_pk130_provenance.