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- NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_assertion type Assertion NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_head.
- NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_assertion wasGeneratedBy ECO_0000203 NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_provenance.
- NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_assertion wasDerivedFrom befree-2016 NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_provenance.
- NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_assertion SIO_000772 19172752 NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_provenance.
- NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_assertion evidence source_evidence_literature NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_provenance.
- NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_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." NP716786.RAD4EH-7RApPILKCgr0f3olJSDxM1JmDMIQmHPiTiSUwk130_provenance.