Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP491713.RA3pjDxCKzbBNy1mnIcVLfWoHxx0RtmlFuVzoiDGz4K-A130_provenance.