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- NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_assertion type Assertion NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_head.
- NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_assertion description "[Because some ARO patients have mutations in both copies of the ClCN7 gene, ADO II is allelic with a subset of ARO cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_provenance.
- NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_assertion evidence source_evidence_literature NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_provenance.
- NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_assertion SIO_000772 11741829 NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_provenance.
- NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_assertion wasDerivedFrom befree-2016 NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_provenance.
- NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_assertion wasGeneratedBy ECO_0000203 NP338744.RAkrywM1oGlE_ZNrheM1v70FZryXEH14RXyAhNlb5l-yE130_provenance.