Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_assertion> ?p ?o ?g. }
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- NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_assertion type Assertion NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_head.
- NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_assertion description "[This work, in addition to clarifying the role of the various TFIIH subunits, supports the current hypothesis that XP-B/D patients are more likely to suffer from transcription repair syndromes rather than DNA repair disorders alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_provenance.
- NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_assertion evidence source_evidence_literature NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_provenance.
- NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_assertion SIO_000772 10064601 NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_provenance.
- NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_assertion wasDerivedFrom befree-20150227 NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_provenance.
- NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_assertion wasGeneratedBy ECO_0000203 NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_provenance.