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- source_evidence_literature type ECO_0000212 NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_provenance.
- NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_assertion description "[Cockayne syndrome (CS) is mainly caused by mutations in the Cockayne syndrome group A or B (CSA or CSB) genes which are required for a sub-pathway of nucleotide excision repair entitled transcription coupled repair.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_provenance.
- NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_assertion evidence source_evidence_literature NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_provenance.
- NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_assertion SIO_000772 17084038 NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_provenance.
- NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_assertion wasDerivedFrom befree-20150227 NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_provenance.
- NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_assertion wasGeneratedBy ECO_0000203 NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP332472.RABFhSBmaBw0qNPDdRELABzBan8YS4SxZT5z5LAGG1h7Q130_provenance.