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- NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_assertion type Assertion NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_head.
- NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_provenance.
- NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_assertion evidence source_evidence_literature NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_provenance.
- NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_assertion SIO_000772 10982188 NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_provenance.
- NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_assertion wasDerivedFrom befree-20150227 NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_provenance.
- NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_assertion wasGeneratedBy ECO_0000203 NP778981.RAx30863w03arAcgzo_hrr6_tslurqHu9c_O6Cxb-67Qg130_provenance.