Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion> ?p ?o ?g. }
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- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion type Assertion NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_head.
- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_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." NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion evidence source_evidence_literature NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion SIO_000772 23623389 NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion wasDerivedFrom befree-20150227 NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.
- NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_assertion wasGeneratedBy ECO_0000203 NP382854.RA042aJiCcUlKD49j9HAa3aPRXfjE2UbXAHRE5HF8ruIU130_provenance.