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- NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_assertion type Assertion NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_head.
- 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.
- NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_assertion evidence source_evidence_literature NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_provenance.
- NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_assertion SIO_000772 20376468 NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_provenance.
- NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_assertion wasDerivedFrom befree-20140225 NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_provenance.
- NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_assertion wasGeneratedBy ECO_0000203 NP486761.RAoAo4x2THZzXAxKz_fAk6P0DPPWNhe1hIdLLx5Lh8sMk130_provenance.