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- source_evidence_literature type ECO_0000212 NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_provenance.
- NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_assertion description "[Finally, the identified MeCP2-YY1 interaction, together with the well-known involvement of YY1 in the regulation of D4Z4-associated genes at 4q35, led us to discover the anomalous depression of FRG2, a subtelomeric gene of unknown function, in Rett fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_provenance.
- NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_assertion evidence source_evidence_literature NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_provenance.
- NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_assertion SIO_000772 20504995 NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_provenance.
- NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_assertion wasDerivedFrom befree-2016 NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_provenance.
- NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_assertion wasGeneratedBy ECO_0000203 NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_provenance.
- befree-2016 importedOn "2016-02-19" NP814917.RATtEHontpVI2GwJD__KGK7OWl4r7S2dcTXfU9jEWy1L8130_provenance.