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- NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_assertion type Assertion NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_head.
- NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_assertion wasGeneratedBy ECO_0000203 NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_provenance.
- NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_assertion wasDerivedFrom befree-2016 NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_provenance.
- NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_assertion SIO_000772 10835633 NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_provenance.
- NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_assertion evidence source_evidence_literature NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_provenance.
- NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_assertion description "[We have isolated LHX3, a gene involved in a new syndrome, using a candidate-gene approach developed on the basis of documented pituitary abnormalities of a recessive lethal mutation in mice generated by targeted disruption of Lhx3 (ref.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285432.RAUnD4DluBaDiK54ficyQt5OoGPHbuyXwvWe9PrWh-93M130_provenance.