Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_assertion> ?p ?o ?g. }
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- NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_assertion type Assertion NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_head.
- NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_assertion wasGeneratedBy ECO_0000203 NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_provenance.
- NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_assertion wasDerivedFrom befree-20140225 NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_provenance.
- NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_assertion SIO_000772 15661754 NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_provenance.
- NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_assertion evidence source_evidence_literature NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_provenance.
- NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_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." NP290670.RA_LbVqfRV2l88Dm_kx18Fjs9WzhqCXAfDJ101gWkv0xw130_provenance.