Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_provenance.
- NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_assertion description "[We postulate that to fully determine whether the sequence differences in VDR gene are susceptibility variants for T2DM, additional studies in different populations are required in a large study group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_provenance.
- NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_assertion evidence source_evidence_literature NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_provenance.
- NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_assertion SIO_000772 14714273 NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_provenance.
- NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_assertion wasDerivedFrom gad-20150221 NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_provenance.
- NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_assertion wasGeneratedBy ECO_0000203 NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_provenance.
- gad-20150221 importedOn "2015-02-21" NP75858.RAqksR6nCaOPZy_JlG9MhHLgQpS1CM-jhBD9XJtsmUU9I130_provenance.