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- source_evidence_literature type ECO_0000212 NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_provenance.
- NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_assertion description "[Variant alleles in xeroderma pigmentosum complementation group C, more than three total variant alleles in all DNA repair genes studied and more than two total variant alleles in three nucleotide excision repair genes were independently associated with improved overall and disease-specific survival of UUT-TCC patients in multivariate analysis (P = .0063 and P = .0005 for xeroderma pigmentosum complementation group C, P = .016 and P = .0016 for all genes, and P = .0053 and P = .018 for nucleotide excision repair genes, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_provenance.
- NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_assertion evidence source_evidence_literature NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_provenance.
- NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_assertion SIO_000772 18320070 NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_provenance.
- NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_assertion wasDerivedFrom befree-20150227 NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_provenance.
- NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_assertion wasGeneratedBy ECO_0000203 NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP779273.RAjGAEEfGg24Q50s_Peg_ymx34FH0DAp8YjUCWGk_7HdU130_provenance.