Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_provenance.
- NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_assertion description "[TCF7L2 codes for the transcription factor TCF/LF, part of the Wnt canonical pathway, and is one of the strongest genetic risk variants for type 2 diabetes (T2D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_provenance.
- NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_assertion evidence source_evidence_literature NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_provenance.
- NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_assertion SIO_000772 24322204 NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_provenance.
- NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_assertion wasDerivedFrom befree-2016 NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_provenance.
- NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_assertion wasGeneratedBy ECO_0000203 NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1135209.RAMVrghIYKPm6iqZqhLMOReXAShkPXbD8LpJEq4f0seV0130_provenance.