Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
• NP692987.RAnoFtxaDQKxMGpeGU9Adzx-0wjpZbjJpV-F2L-ZaAt9s130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692987.RAnoFtxaDQKxMGpeGU9Adzx-0wjpZbjJpV-F2L-ZaAt9s130_provenance.
• NP361953.RADeiaCNYR9Wr7pGPKGUrQrfK4mLKinTnwm93Nt0L4S1s130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361953.RADeiaCNYR9Wr7pGPKGUrQrfK4mLKinTnwm93Nt0L4S1s130_provenance.
• NP362013.RAUSBSIwjUB0LZz1hkcwbda8nCjN0ojjRtM3wj42fsUZU130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362013.RAUSBSIwjUB0LZz1hkcwbda8nCjN0ojjRtM3wj42fsUZU130_provenance.
• NP361991.RA_gxeb9k0A6MLU0xrQGSJEZbKoS4bpeYKJor7Uu21sHE130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361991.RA_gxeb9k0A6MLU0xrQGSJEZbKoS4bpeYKJor7Uu21sHE130_provenance.
• NP362032.RA92sOskTJng3V8_xpAHuOuI2wDNZM1OArqteJn1o6MFk130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362032.RA92sOskTJng3V8_xpAHuOuI2wDNZM1OArqteJn1o6MFk130_provenance.
• assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1092583.RAZbTwywJ7heBQiHb2aZB-0D07HJjDWHjDsvx4vc-lJco130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1092583.RAZbTwywJ7heBQiHb2aZB-0D07HJjDWHjDsvx4vc-lJco130_provenance.
• NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance.
• NP1092585.RAEoEnprsvMZdkUGBk41eC1HB5oylz1mTY-el_xObicMM130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1092585.RAEoEnprsvMZdkUGBk41eC1HB5oylz1mTY-el_xObicMM130_provenance.
• NP1092586.RAqPSsZGRsVTTRejrG8LyED8FkOZn5o0lt35TaXqsj3vw130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1092586.RAqPSsZGRsVTTRejrG8LyED8FkOZn5o0lt35TaXqsj3vw130_provenance.