Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_provenance.
- NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_assertion description "[The results imply that an MRX gene subject to X inactivation is present in a roughly 4 Mb region between DXS7182 and DAX-1, and that reduced expression of the normal MRX gene caused by random X inactivation results in MR in carrier females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_provenance.
- NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_assertion evidence source_evidence_literature NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_provenance.
- NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_assertion SIO_000772 10204842 NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_provenance.
- NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_assertion wasDerivedFrom befree-20140225 NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_provenance.
- NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_assertion wasGeneratedBy ECO_0000203 NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477358.RAQONeQhkGDEPB7dUaoo2Jfc9EiVz-4JN7B5OZylVwXVg130_provenance.