Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_assertion> ?p ?o ?g. }
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- NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_assertion type Assertion NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_head.
- NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_assertion description "[Recently, mutations in a novel gene, PINK1, encoding a 581 amino acid protein with both mitochondrial targeting and serine/threonine kinase domains, were identified as a cause of autosomal recessive parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_provenance.
- NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_assertion evidence source_evidence_literature NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_provenance.
- NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_assertion SIO_000772 16702191 NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_provenance.
- NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_assertion wasDerivedFrom befree-20150227 NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_provenance.
- NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_assertion wasGeneratedBy ECO_0000203 NP374167.RAxN4Vjq03j4CYwOiaaiYj6XZNc7RcTUeMtlCS7eo4EEs130_provenance.