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- NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_assertion type Assertion NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_head.
- NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_assertion description "[Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_provenance.
- NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_assertion evidence source_evidence_literature NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_provenance.
- NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_assertion SIO_000772 22022284 NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_provenance.
- NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_assertion wasDerivedFrom befree-20140225 NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_provenance.
- NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_assertion wasGeneratedBy ECO_0000203 NP689162.RAMKfegkomuXAx0XgFvKezEWlJ51rqEcUQhn6n5e96GNA130_provenance.