Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_assertion> ?p ?o ?g. }
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- NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_assertion type Assertion NP109800.RAJnOaP2aWSh2d0TV-A7aylU6BomHxS3xi-5BzY1Br3Ko130_head.
- 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.