Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_provenance.
- NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_assertion description "[Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_provenance.
- NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_assertion evidence source_evidence_literature NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_provenance.
- NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_assertion SIO_000772 16511860 NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_provenance.
- NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_assertion wasDerivedFrom gad-20150221 NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_provenance.
- NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_assertion wasGeneratedBy ECO_0000203 NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP99258.RAWkFr2UeOGGm2MulUFf-5W3MYBTGoyjOaQIjutBHGUXc130_provenance.