Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_provenance.
- NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_assertion description "[MEFV E148Q polymorphism is associated with Henoch-SchAPnlein purpura in Chinese children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_provenance.
- NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_assertion evidence source_evidence_literature NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_provenance.
- NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_assertion SIO_000772 20602240 NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_provenance.
- NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_assertion wasDerivedFrom gad-20150221 NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_provenance.
- NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_assertion wasGeneratedBy ECO_0000203 NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_provenance.
- gad-20150221 importedOn "2015-02-21" NP180536.RARi0GT4fyu_S2WswI9BuEqmR5H59XRcPuWHezyBz6n3w130_provenance.