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- source_evidence_literature type ECO_0000212 NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_provenance.
- NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_assertion description "[Here we show that Lrrk2 is closely associated with the tau-positive inclusions in eight members of a family with frontotemporal dementia of the pallido-ponto-nigral degeneration type linked to the chromosome 17 N279K tau mutation (N279K/FTDP-17/PPND).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_provenance.
- NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_assertion evidence source_evidence_literature NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_provenance.
- NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_assertion SIO_000772 17639429 NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_provenance.
- NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_assertion wasDerivedFrom befree-2016 NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_provenance.
- NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_assertion wasGeneratedBy ECO_0000203 NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_provenance.
- befree-2016 importedOn "2016-02-19" NP620877.RASD-0XXqmeDcoZUm28gqPYRQjxXKU3TIXgTD3mS0eH4o130_provenance.