Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_provenance.
- NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_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." NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_provenance.
- NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_assertion evidence source_evidence_literature NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_provenance.
- NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_assertion SIO_000772 10204842 NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_provenance.
- NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_assertion wasDerivedFrom befree-20150227 NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_provenance.
- NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_assertion wasGeneratedBy ECO_0000203 NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP823358.RACDMVsj02-4I0AgacSJj80HmE1IR5F64m4_hRNmDrB5I130_provenance.