Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_provenance.
- NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_assertion description "[Defects in the xeroderma pigmentosum type B (XPB) gene (ERCC3), a DNA helicase involved in nucleotide excision repair (NER) and an essential subunit of the basal transcription factor, TFIIH, have been described in only three families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_provenance.
- NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_assertion evidence source_evidence_literature NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_provenance.
- NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_assertion SIO_000772 16947863 NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_provenance.
- NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_assertion wasDerivedFrom befree-20140225 NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_provenance.
- NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_assertion wasGeneratedBy ECO_0000203 NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP359835.RAPa8MZz_Rn9bDLVbHkCFQDoFT44zOrhYtqODxo5ACxKc130_provenance.