Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_assertion type Assertion NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_head.
- NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_assertion description "[report that an autosomal recessive infantile parkinsonism-dystonia is caused by loss-of-function mutations in DAT that impair dopamine reuptake (see the related article beginning on page 1595).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_provenance.
- NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_assertion evidence source_evidence_literature NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_provenance.
- NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_assertion SIO_000772 19504720 NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_provenance.
- NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_assertion wasDerivedFrom befree-20150227 NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_provenance.
- NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_assertion wasGeneratedBy ECO_0000203 NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_provenance.