Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_assertion type Assertion NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_head.
- NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_assertion description "[To date, all identified causative mutations for CS have been in the two known CS-associated genes, ERCC8 (CSA) and ERCC6 (CSB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_provenance.
- NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_assertion evidence source_evidence_literature NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_provenance.
- NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_assertion SIO_000772 23623389 NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_provenance.
- NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_assertion wasDerivedFrom befree-20150227 NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_provenance.
- NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_assertion wasGeneratedBy ECO_0000203 NP314959.RAuTLLGDJFLaJS3xHXls8K1QEBWNyuNK0UMiAr9TZdTrY130_provenance.