Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_provenance.
- NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_assertion description "[MEFV E148Q polymorphism is associated with Henoch-Sch�nlein purpura in Chinese children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_provenance.
- NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_assertion evidence source_evidence_literature NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_provenance.
- NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_assertion SIO_000772 20602240 NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_provenance.
- NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_assertion wasDerivedFrom befree-20150227 NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_provenance.
- NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_assertion wasGeneratedBy ECO_0000203 NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP552564.RAvsRh8aN8shk9mV3xw8wOa-lPprXlCckGLUGZw7B8Kbg130_provenance.