Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_provenance.
- NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_assertion description "[In contrast, no significant difference was observed between the healthy individuals and CML patients in the frequency of polymorphic variants of GSTM1 and CYP1A1 genes (p > 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_provenance.
- NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_assertion evidence source_evidence_literature NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_provenance.
- NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_assertion SIO_000772 21254556 NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_provenance.
- NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_assertion wasDerivedFrom gad-20150221 NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_provenance.
- NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_assertion wasGeneratedBy ECO_0000203 NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP142705.RAc3hVKG9MnQQuMduOuaI1MtdQHzqLYaoF3F_-IIWJsmE130_provenance.