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- NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_assertion type Assertion NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_head.
- NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_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." NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_provenance.
- NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_assertion evidence source_evidence_literature NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_provenance.
- NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_assertion SIO_000772 19172513 NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_provenance.
- NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_assertion wasDerivedFrom gad-20150221 NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_provenance.
- NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_assertion wasGeneratedBy ECO_0000203 NP109801.RAWiHBWOyiQzZW-BGrnywe05j7YbfQB9CeysneQf_ni2I130_provenance.