Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1180460.RAUiEdj-aZdUxEXPyzikp2v8fNIOAEWCNhVXrGVpIReuk130_assertion description "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180460.RAUiEdj-aZdUxEXPyzikp2v8fNIOAEWCNhVXrGVpIReuk130_provenance.
• NP1180461.RAcHP8CtDejP1tpfJWVlyCZuLWvvNCJjoRpHBeBaAESk8130_assertion description "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180461.RAcHP8CtDejP1tpfJWVlyCZuLWvvNCJjoRpHBeBaAESk8130_provenance.
• NP1180466.RAR6oFbq1Zy_PRYo-E38CPaA91GQHSGY3YVqnX7VSYdLE130_assertion description "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180466.RAR6oFbq1Zy_PRYo-E38CPaA91GQHSGY3YVqnX7VSYdLE130_provenance.
• NP1180462.RAg-WBYGGHHy2NTF5NAkdInkstiK-d_RsRzXK3Kjbdapo130_assertion description "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180462.RAg-WBYGGHHy2NTF5NAkdInkstiK-d_RsRzXK3Kjbdapo130_provenance.
• NP1180463.RALjp0CTMvltp56k6lLqe4khoMALEGBQK8in0UcGAFBq0130_assertion description "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180463.RALjp0CTMvltp56k6lLqe4khoMALEGBQK8in0UcGAFBq0130_provenance.
• NP1180464.RA5Rz-2zIcJsUYQ107N3MZAqvkdEzEH22sfYrz8Yentw8130_assertion description "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180464.RA5Rz-2zIcJsUYQ107N3MZAqvkdEzEH22sfYrz8Yentw8130_provenance.
• NP1180465.RAx5iD9bGtq8ZxRdCe9DBo6SwPYUYmWHzKk3mM59fJHmQ130_assertion description "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180465.RAx5iD9bGtq8ZxRdCe9DBo6SwPYUYmWHzKk3mM59fJHmQ130_provenance.
• NP1180467.RA3SdZM6fOcQD8khup4Gll5mokAOshWv1E2EDLkFEpKlg130_assertion description "[The deleted region hereby reported encompassed 34 known genes, including GJA3, GJB2, and GJB6, which are responsible for autosomal recessive deafness, FGF9, which plays crucial roles in embryonic neurological development, and ATP8A2, which causes a cerebellar ataxia and disequilibrium syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180467.RA3SdZM6fOcQD8khup4Gll5mokAOshWv1E2EDLkFEpKlg130_provenance.