Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_assertion> ?p ?o ?g. }
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- NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_assertion type Assertion NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_head.
- NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_assertion wasGeneratedBy ECO_0000203 NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_provenance.
- NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_assertion wasDerivedFrom gad-20150221 NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_provenance.
- NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_assertion SIO_000772 12873860 NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_provenance.
- NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_assertion evidence source_evidence_literature NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_provenance.
- NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_assertion description "[Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80816.RAyPNGJNEE6KSUCAiwt7PELBVvPVTRGDmqpCjOoD3SQZ0130_provenance.