Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_assertion> ?p ?o ?g. }
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- NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_assertion type Assertion NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_head.
- NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_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." NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_provenance.
- NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_assertion evidence source_evidence_literature NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_provenance.
- NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_assertion SIO_000772 10699759 NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_provenance.
- NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_assertion wasDerivedFrom befree-20150227 NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_provenance.
- NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_assertion wasGeneratedBy ECO_0000203 NP441706.RAttCEy85DNEG0dZG3v1OX_PJmX1HqnXTzJ5rn9RT5H0w130_provenance.