Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_provenance.
- befree-2016 importedOn "2016-02-19" NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_provenance.
- NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_assertion wasGeneratedBy ECO_0000203 NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_provenance.
- NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_assertion wasDerivedFrom befree-2016 NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_provenance.
- NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_assertion SIO_000772 23298195 NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_provenance.
- NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_assertion evidence source_evidence_literature NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_provenance.
- NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_assertion description "[Variants in WFS1, CDKN2A/B, KCNJ11, CDC123/CAMK1D, JAZF1, SLC30A8, FTO, CDKAL1, and HHEX/IDE genes are significantly associated with T2DM in She Chinese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1041634.RAiv4VLL-s3mB5tn10m6G042KTiUEDZpM_vc3MGeaWqak130_provenance.