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- NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_assertion type Assertion NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_head.
- NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_assertion description "[Using a novel conditional RP58 allele here we show that its CNS-specific loss yields a novel postnatal phenotype: microencephaly, agenesis of the corpus callosum and cerebellar hypoplasia that resembles the chr1qter deletion microcephaly syndrome in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_provenance.
- NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_assertion evidence source_evidence_literature NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_provenance.
- NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_assertion SIO_000772 22095278 NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_provenance.
- NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_assertion wasDerivedFrom befree-20140225 NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_provenance.
- NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_assertion wasGeneratedBy ECO_0000203 NP410511.RAqt72bo0yew20DHgjJWrhTYCgF2fmjFgkHOF0HbFwoqI130_provenance.