Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_assertion> ?p ?o ?g. }
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- NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_assertion type Assertion NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_head.
- NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_assertion description "[The results of our study suggest that mutations in HNF3B are not a common cause of MODY in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_provenance.
- NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_assertion evidence source_evidence_literature NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_provenance.
- NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_assertion SIO_000772 10868948 NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_provenance.
- NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_assertion wasDerivedFrom befree-20140225 NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_provenance.
- NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_assertion wasGeneratedBy ECO_0000203 NP837109.RAjBZXq6HlCp6M0yTzOIJNzsEmfAbeWVxTyBt20rUMUCI130_provenance.