Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_provenance.
- NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_assertion description "[CFTR and/or SPINK1 gene mutations associate with IP (idiopathic CP and IRAP) independently of the presence of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_provenance.
- NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_assertion evidence source_evidence_literature NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_provenance.
- NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_assertion SIO_000772 21222060 NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_provenance.
- NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_assertion wasDerivedFrom befree-20140225 NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_provenance.
- NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_assertion wasGeneratedBy ECO_0000203 NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP551581.RA-gPZiIf9xcHip3NYE7UkwJe98YZ4J41ZY3BWaetH6lM130_provenance.