Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_provenance.
- NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_assertion description "[In total, we identified 78 potentially damaging rare variants (frequency <1%), including ABCA7 p.L400V in a family with Alzheimer's disease and LRRK2 p.R1514Q in 6 of 98 patients with Parkinson's disease (6.1%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_provenance.
- NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_assertion evidence source_evidence_literature NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_provenance.
- NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_assertion SIO_000772 25174650 NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_provenance.
- NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_assertion wasDerivedFrom befree-2016 NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_provenance.
- NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_assertion wasGeneratedBy ECO_0000203 NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215476.RAJ51XaGpUQz8eA2Oxw9vgx-7flsmunIg1rgn7kqNShvI130_provenance.