Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_provenance.
- NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_assertion description "[In the combined analysis, we identified common genetic variants at six loci (GRB14, ST6GAL1, VPS26A, HMG20A, AP3S2 and HNF4A) newly associated with T2D (P = 4.1 A 10(-8) to P = 1.9 A 10(-11)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_provenance.
- NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_assertion evidence source_evidence_literature NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_provenance.
- NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_assertion SIO_000772 21874001 NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_provenance.
- NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_assertion wasDerivedFrom gad-20150221 NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_provenance.
- NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_assertion wasGeneratedBy ECO_0000203 NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP190167.RABqDyY0coEk3yiUa40mSA1i5LdUICfRHx_lDIMVCHfdI130_provenance.