Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_provenance.
- NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_assertion description "[Although the RecQ helicases WRN and BLM are implicated in the resolution of telomeric secondary structures, very little is known about RECQL4, the RecQ helicase mutated in Rothmund-Thomson syndrome (RTS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_provenance.
- NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_assertion evidence source_evidence_literature NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_provenance.
- NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_assertion SIO_000772 22039056 NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_provenance.
- NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_assertion wasDerivedFrom befree-20140225 NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_provenance.
- NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_assertion wasGeneratedBy ECO_0000203 NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401666.RAG4IhEsWRHCI9BfedBi-xvDFmmMatC-ZEf68v4dC6Urs130_provenance.