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- NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_assertion type Assertion NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_head.
- NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_assertion wasGeneratedBy ECO_0000203 NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_provenance.
- NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_assertion wasDerivedFrom befree-20150227 NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_provenance.
- NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_assertion SIO_000772 24392928 NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_provenance.
- NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_assertion evidence source_evidence_literature NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_provenance.
- NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_assertion description "[Two novel heterozygous mutations were detected: a heterozygous mutation in exon 4 of the TUBA1A gene (c.1160C>T) in a 5-year-old female with microcephaly, severe intellectual disability, and absence of language, and a c.1080 _1084del CCTGAinsACATCTTC in exon 4 of the TUBB2B gene in a 31-year-old female with microcephaly, spastic tetraparesis, severe intellectual disability, and scoliosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986882.RA-TMTRl6dM_buLqfQWGpPQ_IpW_QYRo7VsH4Hr5B6hK4130_provenance.