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- source_evidence_literature type ECO_0000212 NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_provenance.
- NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_assertion description "[Additionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_provenance.
- NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_assertion evidence source_evidence_literature NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_provenance.
- NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_assertion SIO_000772 23761423 NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_provenance.
- NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_assertion wasDerivedFrom befree-2016 NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_provenance.
- NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_assertion wasGeneratedBy ECO_0000203 NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1085472.RANyd94eN7QOO2a2zpug-UFcAPJD3ExR07UVdwCMPC7h8130_provenance.