Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP441766.RAYElFv9o0cz5VGbbTaAgQQmpV1WCdF7wqscEcUlVWco4130_provenance.