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- NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_assertion type Assertion NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_head.
- NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_assertion wasGeneratedBy ECO_0000203 NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_provenance.
- NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_assertion wasDerivedFrom befree-20150227 NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_provenance.
- NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_assertion SIO_000772 19172752 NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_provenance.
- NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_assertion evidence source_evidence_literature NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_provenance.
- NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_assertion description "[Patients with the rare neurodevelopmental repair syndrome known as group A trichothiodystrophy (TTD-A) carry mutations in the gene encoding the p8 subunit of the transcription and DNA repair factor TFIIH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441622.RADGSpi3tUmIfURC18Ag41ym2h97tfkxj9ImU5zCfU8j8130_provenance.