Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_assertion> ?p ?o ?g. }
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- NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_assertion type Assertion NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_head.
- NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_assertion wasGeneratedBy ECO_0000203 NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_provenance.
- NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_assertion wasDerivedFrom befree-20140225 NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_provenance.
- NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_assertion SIO_000772 17728257 NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_provenance.
- NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_assertion evidence source_evidence_literature NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_provenance.
- NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_assertion description "[Because of their high sequence homology, the missense mutations in MMAA that result in methylmalonic aciduria have been mapped onto MeaB and, in conjunction with mutagenesis data, provide possible explanations for the pathology of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP706249.RAnOl0Kd2t71wh4TSLf9SFElYipz8J29q6aaRf3uvTy78130_provenance.