Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_provenance.
- NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_assertion description "[Chromosome 7q32 contains both SNPs and a deletion that were associated to T2D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_provenance.
- NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_assertion evidence source_evidence_literature NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_provenance.
- NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_assertion SIO_000772 18498660 NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_provenance.
- NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_assertion wasDerivedFrom gad-20130706 NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_provenance.
- NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_assertion wasGeneratedBy ECO_0000203 NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_provenance.
- gad-20130706 importedOn "2013-07-06" NP75705.RA5LxXnQKCVRNpD4CyGfuBJe61BD-1XI06yX_tM66S154130_provenance.