Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_provenance.
- NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_assertion description "[Of the five known human RecQ family members, three (BLM, WRN and RECQ4, which cause Bloom's syndrome, Werner's syndrome and Rothmund-Thomson syndrome respectively) are mutated in distinct clinical disorders associated with cancer predisposition and/or premature aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_provenance.
- NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_assertion evidence source_evidence_literature NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_provenance.
- NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_assertion SIO_000772 16246145 NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_provenance.
- NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_assertion wasDerivedFrom befree-2016 NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_provenance.
- NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_assertion wasGeneratedBy ECO_0000203 NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_provenance.
- befree-2016 importedOn "2016-02-19" NP519275.RAieiQ8UIgZ8D79qs8oLyL2IXIRtLx60dewhiw4PILQtU130_provenance.