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- source_evidence_literature type ECO_0000212 NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_provenance.
- NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_assertion description "[Recessively inherited deletions/duplications and point mutations in the parkin gene are the most common cause of early-onset parkinsonism known so far, but in an increasing number of studies, genetic variations in the serine/threonine kinase domain of the PINK1 gene are found to explain early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_provenance.
- NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_assertion evidence source_evidence_literature NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_provenance.
- NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_assertion SIO_000772 19087301 NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_provenance.
- NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_assertion wasDerivedFrom befree-2016 NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_provenance.
- NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_assertion wasGeneratedBy ECO_0000203 NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_provenance.
- befree-2016 importedOn "2016-02-19" NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_provenance.