Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_provenance.
- NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_assertion description "[Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_provenance.
- NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_assertion evidence source_evidence_curated NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_provenance.
- NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_assertion SIO_000772 21640322 NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_provenance.
- NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_assertion wasDerivedFrom gwascat-2016 NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_provenance.
- NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_assertion wasGeneratedBy ECO_0000218 NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_provenance.
- gwascat-2016 importedOn "2016-01-27" NP52863.RAPmajxvzCUAo5ylnC1ShBic2vLCYP7saL9ZLILIrvUsI130_provenance.