Matches in Nanopublications for { ?s ?p "[Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_assertion description "[Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_provenance.