Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_provenance.
- NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_assertion description "[Heterozygous R1215Q mutation is found in atypical hemolytic uremic syndrome, with incomplete penetrance of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_provenance.
- NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_assertion evidence source_evidence_literature NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_provenance.
- NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_assertion SIO_000772 17973958 NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_provenance.
- NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_assertion wasDerivedFrom lhgdn-20090331 NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_provenance.
- NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_assertion wasGeneratedBy ECO_0000203 NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP148960.RANUgB9ZuBUg8jGY3AXD6M8-YOB-dbkBvQlHytGt7jgYk130_provenance.