Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_provenance.
- NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_assertion description "[Controlled for duration of diabetes, the frequency of I/D genotype was not significantly different in 271 subjects with retinopathy (IDDM and NIDDM combined) when compared with 86 subjects without retinopathy at 15 years or more after diagnosis of diabetes (chi 2 = 1.29, df = 2, p = ns).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_provenance.
- NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_assertion evidence source_evidence_literature NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_provenance.
- NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_assertion SIO_000772 8582133 NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_provenance.
- NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_assertion wasDerivedFrom befree-2016 NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_provenance.
- NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_assertion wasGeneratedBy ECO_0000203 NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1346585.RAxCRHVkpu9o7QrXr57WqzQXPZdu4wqe4FLjYR6ffL0jw130_provenance.