Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion> ?p ?o ?g. }
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- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion type Assertion NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_head.
- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion wasGeneratedBy ECO_0000203 NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion wasDerivedFrom befree-20140225 NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion SIO_000772 12134148 NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion evidence source_evidence_literature NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion description "[SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.