Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_assertion> ?p ?o ?g. }
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- NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_assertion type Assertion NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_head.
- NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_assertion description "[A similar issue of differential diagnosis was raised by a large 4.3 Mb 2q22.3q23.1 deletion encompassing ZEB2, the gene responsible for the Mowat-Wilson syndrome, whose signs may overlap with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_provenance.
- NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_assertion evidence source_evidence_literature NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_provenance.
- NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_assertion SIO_000772 20125191 NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_provenance.
- NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_assertion wasDerivedFrom befree-20140225 NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_provenance.
- NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_assertion wasGeneratedBy ECO_0000203 NP546608.RAUhXgSRTDzpzRxB627wX1e5uoIcW0JJ7NxCl1GC7H2GU130_provenance.