Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_provenance.
- NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_assertion wasGeneratedBy ECO_0000203 NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_provenance.
- NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_assertion wasDerivedFrom befree-20150227 NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_provenance.
- NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_assertion SIO_000772 22466610 NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_provenance.
- NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_assertion evidence source_evidence_literature NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_provenance.
- NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_assertion description "[Three of the seven known UV(S)S cases carry mutations in the Cockayne syndrome genes ERCC8 or ERCC6 (also known as CSA and CSB, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP468237.RAGzSV1jL4zwjitnZFy_sxc1rtz2WA_YDkSNFQ0MD03Xg130_provenance.