Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP139732.RAfQpwDPU_70o4WStkvU0_QuHkmRwj3aD40LjhhshoYAg130_provenance.