Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_assertion> ?p ?o ?g. }
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- NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_assertion type Assertion NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_head.
- NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_assertion description "[Recently, mutations in FARS2, which encodes for mitochondrial phenylalanyl-tRNA synthetase, have been implicated in autosomal recessive combined oxidative phosphorylation deficiency 14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_provenance.
- NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_assertion evidence source_evidence_literature NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_provenance.
- NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_assertion SIO_000772 25851414 NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_provenance.
- NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_assertion wasDerivedFrom befree-2016 NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_provenance.
- NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_assertion wasGeneratedBy ECO_0000203 NP1276445.RAv_3SHuFCguGr7UQOX77a-UBKGozdWOcH7lroCENSB0E130_provenance.