Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP911393.RAvs3PqX8QPMiGYTCI5asj4xgzbUCOYA-E65KEoP88jPQ130_provenance.