Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_provenance.
- 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.
- NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_assertion evidence source_evidence_literature NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_provenance.
- NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_assertion SIO_000772 18445050 NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_provenance.
- NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_assertion wasDerivedFrom befree-20140225 NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_provenance.
- NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_assertion wasGeneratedBy ECO_0000203 NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP210233.RA6aXvDd7lA0I003jP1frrK7WNNkAw-wALDavLa6Qcfxk130_provenance.