Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_assertion> ?p ?o ?g. }
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- NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_assertion type Assertion NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_head.
- NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_assertion wasGeneratedBy ECO_0000203 NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_provenance.
- NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_assertion wasDerivedFrom befree-2016 NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_provenance.
- NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_assertion SIO_000772 15661754 NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_provenance.
- NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_assertion evidence source_evidence_literature NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_provenance.
- NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_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." NP477151.RAaRGLRM8EVmstZ7s1N9nuT-BjoSmV_Who8CaEyBVEQLc130_provenance.