Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_assertion> ?p ?o ?g. }
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- NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_assertion type Assertion NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_head.
- 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.
- NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_assertion evidence source_evidence_literature NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_provenance.
- NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_assertion SIO_000772 20376468 NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_provenance.
- NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_assertion wasDerivedFrom befree-2016 NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_provenance.
- NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_assertion wasGeneratedBy ECO_0000203 NP804920.RADuvCSu1YBe3PXM0LPw9EX1uHmzEkqHyFiaaAblfecf8130_provenance.