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- source_evidence_literature type ECO_0000212 NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_provenance.
- NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_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." NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_provenance.
- NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_assertion evidence source_evidence_literature NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_provenance.
- NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_assertion SIO_000772 10064601 NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_provenance.
- NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_assertion wasDerivedFrom befree-20150227 NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_provenance.
- NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_assertion wasGeneratedBy ECO_0000203 NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1009764.RAeNQ7-AoZhsEnVzcPAdo7gEJebNt60jZrNEdi7Zcniqo130_provenance.