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- NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_assertion type Assertion NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_head.
- NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_assertion wasGeneratedBy ECO_0000203 NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_provenance.
- NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_assertion wasDerivedFrom befree-20150227 NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_provenance.
- NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_assertion SIO_000772 23171239 NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_provenance.
- NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_assertion evidence source_evidence_literature NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_provenance.
- NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_assertion description "[Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961923.RAGmX3BNd1Hm0BoymRNlfmL8kNkhuzFdTK8aKcS49tt2Q130_provenance.