Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_provenance.
- NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_assertion description "[Moreover, when XPD mutations prevent interaction with the p44 subunit of TFIIH, transactivation directed by certain nuclear receptors is inhibited, regardless of TTD versus XP phenotype, thus explaining the overlapping symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_provenance.
- NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_assertion evidence source_evidence_literature NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_provenance.
- NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_assertion SIO_000772 12820975 NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_provenance.
- NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_assertion wasDerivedFrom befree-2016 NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_provenance.
- NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_assertion wasGeneratedBy ECO_0000203 NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_provenance.
- befree-2016 importedOn "2016-02-19" NP399126.RA509SPObnDBTRbzLj9hcJTFcDzOBsID1R1X29Xa421DM130_provenance.