Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_assertion> ?p ?o ?g. }
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- NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_assertion type Assertion NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_head.
- NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_assertion wasGeneratedBy ECO_0000203 NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_provenance.
- NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_assertion wasDerivedFrom befree-20140225 NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_provenance.
- NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_assertion SIO_000772 17440947 NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_provenance.
- NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_assertion evidence source_evidence_literature NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_provenance.
- NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_assertion description "[PD patients without autosomal dominant family history or obvious cerebellar ataxia should not be candidates for routine screening of SCA2 or SCA3 mutations for cost-effectiveness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430648.RAjMa2pRb3RE1l1qQrHoBXoorDm_8CdS7hEKSwn-rXZf0130_provenance.