http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13600069

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contentType Journal Article|Research Support, Non-U.S. Gov't
issn 1750-1172
issueIdentifier 1
pageRange 258-
publicationName Orphanet Journal of Rare Diseases
startingPage 258
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bibliographicCitation Zhu Y, Wang R, Cheng Y, Han Y, Li T, Cao Y, Wang B. Analysis of copy number variations of WNT4 gene in a Chinese population with Müllerian anomalies. Orphanet Journal of Rare Diseases. 2021 Jun 07;16(1):258. doi: 10.1186/s13023-021-01888-0.
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date 2021-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/34099025
https://doi.org/10.1186/s13023-021-01888-0
https://pubmed.ncbi.nlm.nih.gov/PMC8183036
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http://rdf.ncbi.nlm.nih.gov/pubchem/journal/32787
language English
source https://scigraph.springernature.com/
https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title Analysis of copy number variations of WNT4 gene in a Chinese population with Müllerian anomalies
discusses http://id.nlm.nih.gov/mesh/M0554343
http://id.nlm.nih.gov/mesh/M0472106

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Predicate Subject
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Total number of triples: 29.