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- NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_assertion type Assertion NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_head.
- NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_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." NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_provenance.
- NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_assertion evidence source_evidence_literature NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_provenance.
- NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_assertion SIO_000772 19172513 NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_provenance.
- NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_assertion wasDerivedFrom gad-20150221 NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_provenance.
- NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_assertion wasGeneratedBy ECO_0000203 NP139731.RASHCj9j2jCFPlbplCvuX6xwRaHTUpnbTx4Tyn0dqd7I0130_provenance.