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- source_evidence_literature type ECO_0000212 NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_provenance.
- NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_assertion description "[In addition to the results demonstrating the involvement of MECP2 in MRX, this study shows that the frequency of mutations in MECP2 in the mentally retarded population screened for the fragile X syndrome is comparable to the frequency of the CGG expansions in FMR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_provenance.
- NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_assertion evidence source_evidence_literature NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_provenance.
- NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_assertion SIO_000772 11309367 NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_provenance.
- NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_assertion wasDerivedFrom befree-20150227 NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_provenance.
- NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_assertion wasGeneratedBy ECO_0000203 NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP551879.RALbizOWc8Ko4lNAPlXWopNQ8_F_MhmKSlVY2tkyvXyiQ130_provenance.