Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_provenance.
- NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_assertion description "[We screened the most common LRRK2 mutation (p.G2019S) in a series of 180 consecutive patients clinically diagnosed with Alzheimer Disease (AD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_provenance.
- NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_assertion evidence source_evidence_literature NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_provenance.
- NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_assertion SIO_000772 19822953 NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_provenance.
- NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_assertion wasDerivedFrom gad-20150221 NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_provenance.
- NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_assertion wasGeneratedBy ECO_0000203 NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP69450.RAXhLh8QZgTT91BKhYuF8JebGS2VQamukj5HMORFFr6Xs130_provenance.