Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_provenance.
• NP784141.RAXa3EXbEqAGWR357DDrZEUfhDyH3Bf41vUWaNlOXlxJ8130_assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784141.RAXa3EXbEqAGWR357DDrZEUfhDyH3Bf41vUWaNlOXlxJ8130_provenance.
• NP841466.RAVM937TlTjJPrTAhZq_GN9Bpq0VtTCHnpxih9zHM52ME130_assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841466.RAVM937TlTjJPrTAhZq_GN9Bpq0VtTCHnpxih9zHM52ME130_provenance.
• assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance.
• NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_provenance.
• NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_provenance.
• NP804916.RAyS1ygyMF7PfBBXZIPhlLrvTyDcVuFjkxkq6zxiA9E04130_assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804916.RAyS1ygyMF7PfBBXZIPhlLrvTyDcVuFjkxkq6zxiA9E04130_provenance.