Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_provenance.
- NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_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." NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_provenance.
- NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_assertion evidence source_evidence_literature NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_provenance.
- NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_assertion SIO_000772 16702191 NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_provenance.
- NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_assertion wasDerivedFrom befree-20150227 NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_provenance.
- NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_assertion wasGeneratedBy ECO_0000203 NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP940609.RAZe7BcTQkhwfEJRjw4zVcFqCN7XBCAB-mUWKOYWFR_qM130_provenance.