Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_assertion> ?p ?o ?g. }
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- NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_assertion type Assertion NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_head.
- NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_assertion description "[Syndromic true hermaphroditism due to an R-spondin1 (RSPO1) homozygous mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_provenance.
- NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_assertion evidence source_evidence_literature NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_provenance.
- NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_assertion SIO_000772 18085567 NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_provenance.
- NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_assertion wasDerivedFrom befree-20140225 NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_provenance.
- NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_assertion wasGeneratedBy ECO_0000203 NP861885.RAgUiEcY6EF9kCFyIh3XgZYRe5GMBpUqmhtpSLTqhWpWQ130_provenance.