Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_assertion> ?p ?o ?g. }
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- NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_assertion type Assertion NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_head.
- NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_assertion wasGeneratedBy ECO_0000203 NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_provenance.
- NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_assertion wasDerivedFrom befree-20150227 NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_provenance.
- NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_assertion SIO_000772 10767341 NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_provenance.
- NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_assertion evidence source_evidence_literature NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_provenance.
- NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_assertion description "[Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332319.RA0LAYn3svljMGYi7tE7Ih48OKppPlxrVP2-4SVH00upY130_provenance.