Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_assertion> ?p ?o ?g. }
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- NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_assertion type Assertion NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_head.
- NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_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." NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance.
- NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_assertion evidence source_evidence_literature NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance.
- NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_assertion SIO_000772 15508018 NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance.
- NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_assertion wasDerivedFrom befree-20140225 NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance.
- NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_assertion wasGeneratedBy ECO_0000203 NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance.