Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_assertion> ?p ?o ?g. }
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- NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_assertion type Assertion NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_head.
- NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_assertion description "[three new exonic LHX4 allelic variants with at least one being responsible for congenital hypopituitarism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_provenance.
- NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_assertion evidence source_evidence_literature NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_provenance.
- NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_assertion SIO_000772 18445675 NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_provenance.
- NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_assertion wasDerivedFrom lhgdn-20090331 NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_provenance.
- NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_assertion wasGeneratedBy ECO_0000203 NP153383.RAgrD7IoJBnj9I7lNiD7EgbUamJ6nLIUlD9B9tfdFjWH4130_provenance.