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- NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_assertion type Assertion NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_head.
- NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_assertion description "[Mutations of the DCTN1 gene have been previously associated with amyotrophic lateral sclerosis and with Perry syndrome, a rare autosomal dominant disorder characterized by weight loss, parkinsonism, central hypoventilation, and psychiatric disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_provenance.
- NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_assertion evidence source_evidence_literature NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_provenance.
- NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_assertion SIO_000772 24343258 NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_provenance.
- NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_assertion wasDerivedFrom befree-20150227 NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_provenance.
- NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_assertion wasGeneratedBy ECO_0000203 NP350613.RAUaYOAD3iQS-wu5SiOV6s-Xqmgau_BWqaS2az7dvQHGQ130_provenance.