Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270376.RAvpikofTgT2taHGa6U23rov2eHsOEp9bTL-IJ67LSDcc130_provenance.
• NP270439.RArztnII95Bc0r9itZOOiSI-esk2RLii4jxgMsw5Gfr8s130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270439.RArztnII95Bc0r9itZOOiSI-esk2RLii4jxgMsw5Gfr8s130_provenance.
• NP918834.RATYHEyp9QgpK8C3CmD_JNY1Xv5_eGEQUIk8phi5kXI5k130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918834.RATYHEyp9QgpK8C3CmD_JNY1Xv5_eGEQUIk8phi5kXI5k130_provenance.
• NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918836.RAtyYTNZ068KL1zhfwj43npRYROPVVXxxthVPFROPKFsQ130_provenance.
• NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270350.RAyCaAxLvP635MIUSmf1IiqB__fzmUPIA9traQT4D8veA130_provenance.
• NP270312.RAF9pLt8M-GgO3QpHQIb-0XM7ovqw246YXHpJH2XewVhc130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270312.RAF9pLt8M-GgO3QpHQIb-0XM7ovqw246YXHpJH2XewVhc130_provenance.
• NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918838.RAEW9aNuEr83Cwt-e2TfuFk1ro3iaWBbkLqfaz5zCiFjY130_provenance.
• NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance.
• NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918835.RA6xvzMEB0xVugP6Jmc6UUepBizKWJF1JsTVo1FIMhC3s130_provenance.