Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_provenance.
- NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_assertion description "[These two PD patients also were characterized by the presence of occasional cytoplasmic TDP-43 inclusions in the temporal cortex, a finding that was not observed in three other patients with the G2019S mutation in LRRK2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_provenance.
- NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_assertion evidence source_evidence_literature NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_provenance.
- NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_assertion SIO_000772 19006185 NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_provenance.
- NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_assertion wasDerivedFrom befree-20140225 NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_provenance.
- NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_assertion wasGeneratedBy ECO_0000203 NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717907.RAqTFlO1BlhUK6WTy_9hQ7O7ieqTIobsRoH3pSbR-Uh4w130_provenance.