Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_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." NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_assertion evidence source_evidence_literature NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_assertion SIO_000772 18445050 NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_assertion wasDerivedFrom befree-20140225 NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_assertion wasGeneratedBy ECO_0000203 NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP389661.RA46Rjlw1TG6tC5FNJ5moDwnxW7wJfy4Vj6Zm8a87pr-w130_provenance.