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- source_evidence_literature type ECO_0000212 NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_provenance.
- NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_provenance.
- NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_assertion evidence source_evidence_literature NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_provenance.
- NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_assertion SIO_000772 15508018 NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_provenance.
- NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_assertion wasDerivedFrom befree-2016 NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_provenance.
- NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_assertion wasGeneratedBy ECO_0000203 NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_provenance.
- befree-2016 importedOn "2016-02-19" NP466319.RAN-su9tZbhiou_JkW_0givt3OoknObbhspYV2XGmFeGY130_provenance.