Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_assertion> ?p ?o ?g. }
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- NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_assertion type Assertion NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_head.
- NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_assertion wasGeneratedBy ECO_0000203 NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_provenance.
- NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_assertion wasDerivedFrom lhgdn-20090331 NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_provenance.
- NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_assertion SIO_000772 18429043 NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_provenance.
- NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_assertion evidence source_evidence_literature NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_provenance.
- NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_assertion description "[Based on our results it is estimated that about 20% of patients with Usher syndrome type I have CDH23 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237040.RAh0pTCHJwRV-peQZIVo5DEHrRctshWRNfGmAw50DXCvE130_provenance.