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- NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_assertion type Assertion NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_head.
- NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_assertion wasGeneratedBy ECO_0000218 NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_provenance.
- NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_assertion wasDerivedFrom uniprot-2016 NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_provenance.
- NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_assertion SIO_000772 22405087 NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_provenance.
- NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_assertion evidence source_evidence_curated NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_provenance.
- NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_assertion description "[Infantile cerebellar-retinal degeneration associated with a mutation in mitochondrial aconitase, ACO2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6995.RADiQ_1EecBX9B1WXFj7wHeisvssi3vVPGU_225amJlWI130_provenance.