Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_assertion> ?p ?o ?g. }
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- NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_assertion type Assertion NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_head.
- NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_assertion description "[De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature review.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_provenance.
- NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_assertion evidence source_evidence_literature NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_provenance.
- NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_assertion SIO_000772 25851617 NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_provenance.
- NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_assertion wasDerivedFrom befree-2016 NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_provenance.
- NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_assertion wasGeneratedBy ECO_0000203 NP1276449.RAaTmT-TKBENe6etg7nBhqwxmn5AW_037I2DYYFpoRu5Q130_provenance.