Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_provenance.
- NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_assertion description "[Genes that significantly influence CCT can be candidate genes for common disorders in which CCT has been implicated, such as primary open-angle glaucoma (POAG) and keratoconus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_provenance.
- NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_assertion evidence source_evidence_literature NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_provenance.
- NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_assertion SIO_000772 21984434 NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_provenance.
- NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_assertion wasDerivedFrom befree-20140225 NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_provenance.
- NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_assertion wasGeneratedBy ECO_0000203 NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP749096.RAgWt0s58bal29XG4c0ixRSUFOlKakRDBwt7Ada3Ov12I130_provenance.