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- NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_assertion type Assertion NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_head.
- NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_assertion description "[Molecular diagnosis is provided by the identification of a mutation in the OPA1 gene (75% of DOA patients) or in the OPA3 gene (1% of patients).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_provenance.
- NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_assertion evidence source_evidence_literature NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_provenance.
- NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_assertion SIO_000772 22776096 NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_provenance.
- NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_assertion wasDerivedFrom befree-2016 NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_provenance.
- NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_assertion wasGeneratedBy ECO_0000203 NP996192.RAavCnfoyNAP-GWhTpHOvodBgOHw1PR1JNqfJi8d2hQn8130_provenance.