Matches in Nanopublications for { ?s ?p "[the 35delG mutation was determined as the most frequently shown mutation that leads to congenital hearing loss as in previous studies from Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_assertion description "[the 35delG mutation was determined as the most frequently shown mutation that leads to congenital hearing loss as in previous studies from Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance.
- NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_assertion description "[the 35delG mutation was determined as the most frequently shown mutation that leads to congenital hearing loss as in previous studies from Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance.
- assertion description "[the 35delG mutation was determined as the most frequently shown mutation that leads to congenital hearing loss as in previous studies from Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP124658.RAIZMcdugnSm6wmDnzszoVMp80ILD6Rg6l-5j97kCNYS8130_assertion description "[the 35delG mutation was determined as the most frequently shown mutation that leads to congenital hearing loss as in previous studies from Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP124658.RAIZMcdugnSm6wmDnzszoVMp80ILD6Rg6l-5j97kCNYS8130_provenance.