Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_assertion> ?p ?o ?g. }
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- NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_assertion type Assertion NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_head.
- NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_assertion description "[In contrast, mutations in two members of the TFIIH complex, the XPB and XPD genes are generally very severe with both skin and CNS disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_provenance.
- NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_assertion evidence source_evidence_literature NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_provenance.
- NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_assertion SIO_000772 10699759 NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_provenance.
- NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_assertion wasDerivedFrom befree-20140225 NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_provenance.
- NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_assertion wasGeneratedBy ECO_0000203 NP471941.RAwYw7If3nbR527pxtFx-CZhQu6pxlLBGsPXEcI3c3ZNY130_provenance.