Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_assertion> ?p ?o ?g. }
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- NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_assertion type Assertion NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_head.
- NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_assertion description "[This study screened WNT4 for mutation in 189 Chinese women with M�llerian duct abnormalities (10 Mayer-Rokitansky-K�ster-Hauser syndrome, five M�llerian aplasia and 174 incomplete M�llerian fusion) and detected no perturbation that would indicate a major role for WNT4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_provenance.
- NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_assertion evidence source_evidence_literature NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_provenance.
- NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_assertion SIO_000772 22503279 NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_provenance.
- NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_assertion wasDerivedFrom befree-2016 NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_provenance.
- NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_assertion wasGeneratedBy ECO_0000203 NP974766.RAvqhbCyvP88Pe4VGenzshMd23StwS6IE31kCuJyn-YJk130_provenance.