Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_provenance.
- NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_assertion description "[Clinical features were compared between patients with genetically undefined PD (n=107) and those with LRRK2 (n=73) and PINK1 (n=42) mutations using regression analyses adjusted for gender, age of onset and disease duration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_provenance.
- NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_assertion evidence source_evidence_literature NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_provenance.
- NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_assertion SIO_000772 19726410 NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_provenance.
- NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_assertion wasDerivedFrom befree-20140225 NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_provenance.
- NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_assertion wasGeneratedBy ECO_0000203 NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP174568.RAz22gNEc9E2CpZA-awrp04IH6gYQnkUU8aJ59YZVLD_I130_provenance.