Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP731475.RAA-IJdARRgHW4TlXA9sdBALJ0rdKYxggUFoKF0KRKdGM130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP731475.RAA-IJdARRgHW4TlXA9sdBALJ0rdKYxggUFoKF0KRKdGM130_provenance.
• NP717874.RADYnm6hojGnsCH1-YId00-Bpm39jXZDo5X9gcadIkT6k130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717874.RADYnm6hojGnsCH1-YId00-Bpm39jXZDo5X9gcadIkT6k130_provenance.
• NP908961.RAXtH4ZfVsWHz3OXPdgyDzUxdtivJ5POOnubTmKYZtMrs130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908961.RAXtH4ZfVsWHz3OXPdgyDzUxdtivJ5POOnubTmKYZtMrs130_provenance.
• NP743421.RAwotrhyAFWgsZWALVSlMLRmPWJu_-UVwP-1lrZ_Ct4_Y130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743421.RAwotrhyAFWgsZWALVSlMLRmPWJu_-UVwP-1lrZ_Ct4_Y130_provenance.
• NP501767.RAN__j9V66f8yIzcw8-sfmzd3s7jJbtyL9XpycXDPDbW0130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501767.RAN__j9V66f8yIzcw8-sfmzd3s7jJbtyL9XpycXDPDbW0130_provenance.
• NP905615.RAU7LfHGqDTuCxs-HJzEDkiChbgGznjpdITVgOxGp_12w130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905615.RAU7LfHGqDTuCxs-HJzEDkiChbgGznjpdITVgOxGp_12w130_provenance.
• NP1017500.RAB-Rl8NdkrljJ8QDs6qQsFe8Vlv8b1FEZu6xkwdkaftw130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1017500.RAB-Rl8NdkrljJ8QDs6qQsFe8Vlv8b1FEZu6xkwdkaftw130_provenance.
• assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP854922.RAd-907re13og6vpVv5CGEVj5Rh6wF4V42ls_LmHS_Sw0130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854922.RAd-907re13og6vpVv5CGEVj5Rh6wF4V42ls_LmHS_Sw0130_provenance.
• NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854921.RAgAySx-_ErWTKsK90o1YI4DZcbcyeeVhO6Xw5c5YbSXY130_provenance.
• NP675078.RAxF2PopKXOmDxbvbtsR8hO1LOxhaR-sCdT1onSkxeCBk130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675078.RAxF2PopKXOmDxbvbtsR8hO1LOxhaR-sCdT1onSkxeCBk130_provenance.
• NP990790.RA8t9hQck1l2wj-c-5rcr4MJp3xwEvCr9h_Vc1SvSsGEY130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990790.RA8t9hQck1l2wj-c-5rcr4MJp3xwEvCr9h_Vc1SvSsGEY130_provenance.
• NP1016219.RA8e9FIme_xgoF1cdSwgpQ8WQE7kLhaSz4TE4AvVNrquo130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1016219.RA8e9FIme_xgoF1cdSwgpQ8WQE7kLhaSz4TE4AvVNrquo130_provenance.
• NP854923.RA50qbQTpRZ-AjN5EP_qfA3C1p-DCBM-0OEimExX4j5fE130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854923.RA50qbQTpRZ-AjN5EP_qfA3C1p-DCBM-0OEimExX4j5fE130_provenance.
• NP854924.RA5P5gREawTK5q-G6ETAjd6slfGSB2EZwHLlWV3zt7-xQ130_assertion description "[Analysis of affected families allowed narrowing of the candidate region on chromosome 15q22.31, and mutation screening led to the identification of a previously uncharacterized gene, KBTBD13, coding for a hypothetical protein and containing missense mutations that perfectly cosegregate with nemaline myopathy in the studied families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854924.RA5P5gREawTK5q-G6ETAjd6slfGSB2EZwHLlWV3zt7-xQ130_provenance.