Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_provenance.
- NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_assertion description "[In conclusion, IDDM7 (D2S152) links to IDDM in Danish patients, but D2S2363 and the identified T284A polymorphism in the GALNT3 3'UTR did not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_provenance.
- NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_assertion evidence source_evidence_literature NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_provenance.
- NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_assertion SIO_000772 10679951 NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_provenance.
- NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_assertion wasDerivedFrom befree-20140225 NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_provenance.
- NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_assertion wasGeneratedBy ECO_0000203 NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP307971.RAcGsLCbP5Nff4yNhrD07ME9OB_KInGCe9VcrKh3ouJTQ130_provenance.