Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_provenance.
- NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_assertion description "[We have shown for the first time that variants at WFS1, JAZF1, SLC30A8, CDKN2A/B, TCF7L2, KCNQ1, HMG20A, HNF4A and DUSP9 are associated with T2D in the Saudi population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_provenance.
- NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_assertion evidence source_evidence_literature NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_provenance.
- NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_assertion SIO_000772 23448427 NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_provenance.
- NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_assertion wasDerivedFrom befree-20150227 NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_provenance.
- NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_assertion wasGeneratedBy ECO_0000203 NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977970.RAtlLyn8C99AChhzff7DjUuV8KVR9upY6W_xJYyZRiHQo130_provenance.