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- NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_assertion type Assertion NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_head.
- NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_assertion wasGeneratedBy ECO_0000203 NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_provenance.
- NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_assertion wasDerivedFrom befree-20150227 NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_provenance.
- NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_assertion SIO_000772 14506070 NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_provenance.
- NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_assertion evidence source_evidence_literature NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_provenance.
- NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914834.RAUUdejtYtP9nk1L0vGhenf4gKS7Ap7UbhDn-vOnd_464130_provenance.