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- NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_assertion type Assertion NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_head.
- NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_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." NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_provenance.
- NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_assertion evidence source_evidence_literature NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_provenance.
- NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_assertion SIO_000772 17084038 NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_provenance.
- NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_assertion wasDerivedFrom befree-20140225 NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_provenance.
- NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_assertion wasGeneratedBy ECO_0000203 NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_provenance.