Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_provenance.
- NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_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." NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_provenance.
- NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_assertion evidence source_evidence_literature NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_provenance.
- NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_assertion SIO_000772 10699759 NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_provenance.
- NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_assertion wasDerivedFrom befree-20150227 NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_provenance.
- NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_assertion wasGeneratedBy ECO_0000203 NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382389.RAhX2A1WGeFuwix0yG2RRmNw625Tto60yavQ7CB0rYa3c130_provenance.