Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_assertion> ?p ?o ?g. }
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- NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_assertion type Assertion NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_head.
- NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_assertion wasGeneratedBy ECO_0000218 NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_provenance.
- NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_assertion wasDerivedFrom uniprot-20150221 NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_provenance.
- NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_assertion SIO_000772 23103230 NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_provenance.
- NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_assertion evidence source_evidence_curated NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_provenance.
- NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_assertion description "[In-frame mutations in exon 1 of SKI cause dominant Shprintzen-Goldberg syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1575.RAGWrOXKyyQN42sA3xMhR2HnW-6g4LZPgyN1tLXhnODdg130_provenance.