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- source_evidence_literature type ECO_0000212 NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_provenance.
- befree-2016 importedOn "2016-02-19" NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_provenance.
- NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_assertion wasGeneratedBy ECO_0000203 NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_provenance.
- NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_assertion wasDerivedFrom befree-2016 NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_provenance.
- NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_assertion SIO_000772 15661754 NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_provenance.
- NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_assertion evidence source_evidence_literature NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_provenance.
- NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_assertion description "[Both the total number of chromosome gaps and breaks and breaks at the specific common fragile sites FRA3B and FRA16D were significantly elevated in the absence of an intact FA pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477147.RAWx8jZX0ypAhWO9cjTXF_WL4jkLbj5rTXgUsBIXhJ6Og130_provenance.