Matches in Nanopublications for { ?s ?p "[Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP714405.RAmeY4L_QZqZe_sNKCTpAZmoPgMjEv-fAkZ39lCUc1Px8130_assertion description "[Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714405.RAmeY4L_QZqZe_sNKCTpAZmoPgMjEv-fAkZ39lCUc1Px8130_provenance.
- NP783597.RASGaQPhKa7S_Ex-wKQJZSap9nsE4PF1uGgi9RcM7dGgY130_assertion description "[Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783597.RASGaQPhKa7S_Ex-wKQJZSap9nsE4PF1uGgi9RcM7dGgY130_provenance.
- assertion description "[Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP783647.RAs6E7SnLw1J8l1xHeMakHJlndyt7F5pIqktQ3h4depmE130_assertion description "[Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783647.RAs6E7SnLw1J8l1xHeMakHJlndyt7F5pIqktQ3h4depmE130_provenance.
- NP754761.RAQ_PDw113_zCMmZfcjeJm8F-jpCKk3dzYkeaEYhu3qlQ130_assertion description "[Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754761.RAQ_PDw113_zCMmZfcjeJm8F-jpCKk3dzYkeaEYhu3qlQ130_provenance.
- NP754762.RAWf9Tut1nGYijMGWhFVReUbMdC4CNsJxxCM2eQ7BKRlU130_assertion description "[Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754762.RAWf9Tut1nGYijMGWhFVReUbMdC4CNsJxxCM2eQ7BKRlU130_provenance.