Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_provenance.
• NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196698.RAnSN4hlP8li7Jt5QQeddeGU5QXzbNkjqFb73SwceC_sA130_provenance.
• NP902745.RAUA2xBL6huLUzpWXTURgZbtEZ8UzQ_mOTVc3K3nmwiNE130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902745.RAUA2xBL6huLUzpWXTURgZbtEZ8UzQ_mOTVc3K3nmwiNE130_provenance.
• NP861428.RA5R6IFZYIWkKH0_Jgh2tn08linnqOKvTbR09JjRSkSng130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP861428.RA5R6IFZYIWkKH0_Jgh2tn08linnqOKvTbR09JjRSkSng130_provenance.
• NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651697.RAOwzapA1rWfywLWgeanOa9JTDvpkAMlxLkw69py_-pCg130_provenance.
• NP252296.RAecOkC7p_mYoqEF4QDU71QAMzuZTWq3eprwuHOlWHn3I130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252296.RAecOkC7p_mYoqEF4QDU71QAMzuZTWq3eprwuHOlWHn3I130_provenance.
• NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252295.RAhHFok84YrevC7VgMnOeqnDh63I2YQXYEZVWF6SI_OmM130_provenance.
• NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance.
• NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_provenance.
• NP252294.RAHYo1f9mEvkWs9wV4JLjiOAS1roklgPVXn-jiv8BEKlk130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252294.RAHYo1f9mEvkWs9wV4JLjiOAS1roklgPVXn-jiv8BEKlk130_provenance.
• NP252297.RAL8IzBK7bbIbC3kLM-UKTlCONVEofbIXMUVc5fj2gP_k130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252297.RAL8IzBK7bbIbC3kLM-UKTlCONVEofbIXMUVc5fj2gP_k130_provenance.
• NP902763.RAMI5s-AzsOmwhKEPUQUapfdWkW-MDzfFbaF8JDXmdZh4130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902763.RAMI5s-AzsOmwhKEPUQUapfdWkW-MDzfFbaF8JDXmdZh4130_provenance.