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- source_evidence_literature type ECO_0000212 NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_provenance.
- NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_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." NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_provenance.
- NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_assertion evidence source_evidence_literature NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_provenance.
- NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_assertion SIO_000772 19822953 NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_provenance.
- NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_assertion wasDerivedFrom gad-20150221 NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_provenance.
- NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_assertion wasGeneratedBy ECO_0000203 NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP157903.RAk5imtUytqX-Ssj3A65gbnWgkySpU8e9h3mp5_N6oXCs130_provenance.