Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_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.
- NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_assertion evidence source_evidence_literature NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_provenance.
- NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_assertion SIO_000772 18445050 NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_provenance.
- NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_assertion wasDerivedFrom befree-2016 NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_provenance.
- NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_assertion wasGeneratedBy ECO_0000203 NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_provenance.
- befree-2016 importedOn "2016-02-19" NP668465.RARBMQvge92r7QYYBzpJPsu1O8IyGF7dY6pW_3K_Isb30130_provenance.