Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_provenance.
- NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_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." NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_provenance.
- NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_assertion evidence source_evidence_literature NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_provenance.
- NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_assertion SIO_000772 22039056 NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_provenance.
- NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_assertion wasDerivedFrom befree-20150227 NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_provenance.
- NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_assertion wasGeneratedBy ECO_0000203 NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP268121.RAAQacL2-N2sNeKgSlEkNAxa8Cf_lqi2vfPVUeu0BQzrc130_provenance.