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DESCRIBE <http://purl.uniprot.org/SHA-384/80FF8280B4BBD878939D475253A23F6AA24976B48E9C236D9E4B2B2494C0997B0B8DFDA772350CFC527B2B0F0E45029D>
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http://purl.uniprot.org/SHA-384/80FF8280B4BBD878939D475253A23F6AA24976B48E9C236D9E4B2B2494C0997B0B8DFDA772350CFC527B2B0F0E45029D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/80FF8280B4BBD878939D475253A23F6AA24976B48E9C236D9E4B2B2494C0997B0B8DFDA772350CFC527B2B0F0E45029D
http://www.w3.org/2000/01/rdf-schema#comment
"Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Kuster-Hauser syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_0EBA74D37FAEB326878AB54675C75BE03D85D80EEEB163017059C33FC152DDADC0FE528ED08EA8B99C9E7341087B7C87
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/80FF8280B4BBD878939D475253A23F6AA24976B48E9C236D9E4B2B2494C0997B0B8DFDA772350CFC527B2B0F0E45029D
http://purl.uniprot.org/uniprot/Q9C091
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/80FF8280B4BBD878939D475253A23F6AA24976B48E9C236D9E4B2B2494C0997B0B8DFDA772350CFC527B2B0F0E45029D
http://purl.uniprot.org/uniprot/#_Q9C091-mappedCitation-37124138
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/80FF8280B4BBD878939D475253A23F6AA24976B48E9C236D9E4B2B2494C0997B0B8DFDA772350CFC527B2B0F0E45029D