Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_provenance.
- NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_assertion description "[This result shows that mutation in LCA5 is likely to be a rare genetic cause in Koreans and suggests that further investigation to identify other causative genes is necessary in Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_provenance.
- NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_assertion evidence source_evidence_literature NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_provenance.
- NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_assertion SIO_000772 19172513 NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_provenance.
- NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_assertion wasDerivedFrom gad-20150221 NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_provenance.
- NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_assertion wasGeneratedBy ECO_0000203 NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_provenance.
- gad-20150221 importedOn "2015-02-21" NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_provenance.