Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_provenance.
- NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_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." NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_provenance.
- NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_assertion evidence source_evidence_literature NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_provenance.
- NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_assertion SIO_000772 22039056 NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_provenance.
- NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_assertion wasDerivedFrom befree-2016 NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_provenance.
- NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_assertion wasGeneratedBy ECO_0000203 NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_provenance.
- befree-2016 importedOn "2016-02-19" NP934950.RAhE95M3uzfJU9fqjR1ZwYHRRcBUsAcXrYQXJhROt6dvs130_provenance.