Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_provenance.
- NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_assertion description "[To investigate the distribution of polymorphisms in the PAX2 gene in children with Henoch-Schonlein purpura with and without nephritis (HSPN and HSP, respectively), with particular attention to the relationship between PAX2 gene polymorphisms and the development of kidney pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_provenance.
- NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_assertion evidence source_evidence_literature NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_provenance.
- NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_assertion SIO_000772 16509931 NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_provenance.
- NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_assertion wasDerivedFrom befree-20150227 NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_provenance.
- NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_assertion wasGeneratedBy ECO_0000203 NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP469180.RAOqV14apVuJiCYZaPYO4nve6nLDk899rfqv7XsR7_xEg130_provenance.