Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP698564.RAi_Qg5gKMBPY6doxhcjnKpEhCtaJBzLAYvCZs5KVwZ1A130_provenance.