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- NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_assertion type Assertion NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_head.
- NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_provenance.
- NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_assertion evidence source_evidence_literature NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_provenance.
- NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_assertion SIO_000772 19089472 NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_provenance.
- NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_assertion wasDerivedFrom befree-2016 NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_provenance.
- NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_assertion wasGeneratedBy ECO_0000203 NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_provenance.