Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_assertion type Assertion NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_head.
- NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_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." NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_provenance.
- NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_assertion evidence source_evidence_literature NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_provenance.
- NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_assertion SIO_000772 19172513 NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_provenance.
- NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_assertion wasDerivedFrom gad-20150221 NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_provenance.
- NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_assertion wasGeneratedBy ECO_0000203 NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_provenance.